Component

Calcium

Nutritional calcium element; distinct from free Ca2+, salts, mineral deposits and calcium-signaling events. Nutritional element; not elemental metal exposure, free calcium ion, or a specific calcium salt. Forms and intake are recorded in each event.

48 recorded relationships. Experimental role, claim status and evidence remain attached to each record.

How nutrients influence it

Every nutrient with a recorded effect on this component, credited to the nutrient that acted rather than the chapter that recorded it. Open a nutrient to see the findings and the conditions they were measured under.

How nutrients reach it in more than one step

Chains of two or more recorded steps that end here, grouped by the nutrient they start from. Each step is a separate finding, so a chain is a route a mechanism could take, not proof that it does.

Tracing routes…

What it does

Every recorded relationship this component is part of, grouped by its role. Plain wording comes first; the technical statement follows.

Recorded relationships

What it acts on

  1. Higher calcium intake did not significantly alter Mg absorption, excretion or modeled balance in five adolescent girls.

    Calcium → Whole-body magnesium balance source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Calcium -> magnesium balance: a bounded null interaction.
    experimental_model
    Randomized crossover; Mg isotope kinetics.
    exposure
    Calcium 800 versus 1800 mg/day; Mg intakes about 305 versus 286 mg/day.
    limitations
    Very small and population-specific; a null result is not equivalence for all intakes or ages.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Homo sapiens
    plain_language
    Calcium and magnesium do not always compete enough to change measured balance.
    primary_references
    [mg-sojka1997] Magnesium kinetics in adolescent girls determined using stable isotopes: effects of high and low calcium intake (1997). https://pubmed.ncbi.nlm.nih.gov/9277559/ DOI: 10.1152/ajpregu.1997.273.2.r710
    tissue_or_cell_type
    Human whole-body Mg isotope kinetics

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 1615–1626

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized crossover; Mg isotope kinetics. · source_derived_draft · unverified_draft

    ### mg-high-calcium-no-kinetic-difference Higher calcium intake did not significantly alter Mg absorption, excretion or modeled balance in five adolescent girls. Condition category: normal nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium and magnesium do not always compete enough to change measured balance. organism: Homo sapiens tissue_or_cell_type: Human whole-body Mg isotope kinetics experimental_model: Randomized crossover; Mg isotope kinetics. limitations: Very small and population-specific; a null result is not equivalence for all intakes or ages. cross_nutrient: Calcium -> magnesium balance: a bounded null interaction. exposure: Calcium 800 versus 1800 mg/day; Mg intakes about 305 versus 286 mg/day. [mg-sojka1997] Magnesium kinetics in adolescent girls determined using stable isotopes: effects of high and low calcium intake (1997). https://pubmed.ncbi.nlm.nih.gov/9277559/ DOI: 10.1152/ajpregu.1997.273.2.r710
    Complete structured claim and evidence
  2. An older-women calcium trial showed an upward myocardial-infarction signal that weakened when registry events were added.

    Calcium → Myocardial infarction incidence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    1471 postmenopausal women, five-year randomized trial; secondary cardiovascular analysis.
    exposure
    Calcium citrate tablets versus placebo in the parent randomized trial; calcium-only intervention, not the WHI calcium-plus-vitamin-D regimen.
    limitations
    Adjudicated reported MI RR 2.12 (1.01-4.47); including unreported registry events RR 1.49 (0.86-2.57). Does not establish vascular calcification as the mediator.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The heart-event result depended partly on how events were collected.
    primary_references
    [cal-clin-bolland2008] Vascular events in healthy older women receiving calcium supplementation: randomised controlled trial (2008). https://pubmed.ncbi.nlm.nih.gov/18198394/ DOI: 10.1136/bmj.39440.525752.BE
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1281–1291

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 1471 postmenopausal women, five-year randomized trial; secondary cardiovascular analysis. · source_derived_draft · unverified_draft

    ### cal-bolland-myocardial-events An older-women calcium trial showed an upward myocardial-infarction signal that weakened when registry events were added. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The heart-event result depended partly on how events were collected. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 1471 postmenopausal women, five-year randomized trial; secondary cardiovascular analysis. limitations: Adjudicated reported MI RR 2.12 (1.01-4.47); including unreported registry events RR 1.49 (0.86-2.57). Does not establish vascular calcification as the mediator. exposure: Calcium citrate tablets versus placebo in the parent randomized trial; calcium-only intervention, not the WHI calcium-plus-vitamin-D regimen. [cal-clin-bolland2008] Vascular events in healthy older women receiving calcium supplementation: randomised controlled trial (2008). https://pubmed.ncbi.nlm.nih.gov/18198394/ DOI: 10.1136/bmj.39440.525752.BE
    Complete structured claim and evidence
  3. A normal-calcium diet with less animal protein and salt reduced stone recurrence compared with a low-calcium diet.

    Calcium → Calcium oxalate stone recurrence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    120 hypercalciuric male recurrent stone formers; five-year randomized comparison.
    exposure
    Recurrences 12/60 versus 23/60; RR 0.49, 95% CI 0.24-0.98. Calcium 30 versus 10 mmol/day; intervention also reduced animal protein and salt.
    limitations
    Multiple dietary components changed together, preventing isolated calcium attribution.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Restricting calcium was not the better strategy in this particular dietary trial.
    primary_references
    [cal-clin-borghi2002] Comparison of two diets for the prevention of recurrent stones in idiopathic hypercalciuria (2002). https://pubmed.ncbi.nlm.nih.gov/11784873/ DOI: 10.1056/NEJMoa010369
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1235–1245

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 120 hypercalciuric male recurrent stone formers; five-year randomized comparison. · source_derived_draft · unverified_draft

    ### cal-borghi-stone-recurrence A normal-calcium diet with less animal protein and salt reduced stone recurrence compared with a low-calcium diet. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Restricting calcium was not the better strategy in this particular dietary trial. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 120 hypercalciuric male recurrent stone formers; five-year randomized comparison. limitations: Multiple dietary components changed together, preventing isolated calcium attribution. exposure: Recurrences 12/60 versus 23/60; RR 0.49, 95% CI 0.24-0.98. Calcium 30 versus 10 mmol/day; intervention also reduced animal protein and salt. [cal-clin-borghi2002] Comparison of two diets for the prevention of recurrent stones in idiopathic hypercalciuria (2002). https://pubmed.ncbi.nlm.nih.gov/11784873/ DOI: 10.1056/NEJMoa010369
    Complete structured claim and evidence
  4. Urinary oxalate rose with the low-calcium diet but fell with the normal-calcium, lower-protein, lower-salt diet.

    Calcium → Urinary oxalate excretion source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Same randomized dietary trial.
    limitations
    Urine result supports a plausible intestinal explanation but does not isolate binding or prove mediation of recurrence.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Diet composition changed urinary oxalate as well as calcium.
    primary_references
    [cal-clin-borghi2002] Comparison of two diets for the prevention of recurrent stones in idiopathic hypercalciuria (2002). https://pubmed.ncbi.nlm.nih.gov/11784873/ DOI: 10.1056/NEJMoa010369
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1247–1256

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Same randomized dietary trial. · source_derived_draft · unverified_draft

    ### cal-borghi-urinary-oxalate Urinary oxalate rose with the low-calcium diet but fell with the normal-calcium, lower-protein, lower-salt diet. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Diet composition changed urinary oxalate as well as calcium. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Same randomized dietary trial. limitations: Urine result supports a plausible intestinal explanation but does not isolate binding or prove mediation of recurrence. [cal-clin-borghi2002] Comparison of two diets for the prevention of recurrent stones in idiopathic hypercalciuria (2002). https://pubmed.ncbi.nlm.nih.gov/11784873/ DOI: 10.1056/NEJMoa010369
    Complete structured claim and evidence
  5. Combined calcium and vitamin D lowered hip-fracture occurrence in the elderly-women trial.

    Calcium → Hip fracture incidence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    3270 elderly women; mean age 84; 18-month randomized trial.
    exposure
    1.2 g elemental calcium as tricalcium phosphate plus 800 IU vitamin D3/day; 43% lower hip-fracture count among completers, with similar direction in intention-to-treat analysis.
    limitations
    Calcium-specific attribution is impossible because vitamin D was coadministered. Completer and intention-to-treat analyses must be distinguished.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    A combined intervention reduced fractures in this older population.
    primary_references
    [cal-clin-chapuy1992] Vitamin D3 and calcium to prevent hip fractures in elderly women (1992). https://pubmed.ncbi.nlm.nih.gov/1331788/ DOI: 10.1056/NEJM199212033272305
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1199–1209

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 3270 elderly women; mean age 84; 18-month randomized trial. · source_derived_draft · unverified_draft

    ### cal-chapuy-hip-fractures Combined calcium and vitamin D lowered hip-fracture occurrence in the elderly-women trial. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: A combined intervention reduced fractures in this older population. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 3270 elderly women; mean age 84; 18-month randomized trial. limitations: Calcium-specific attribution is impossible because vitamin D was coadministered. Completer and intention-to-treat analyses must be distinguished. exposure: 1.2 g elemental calcium as tricalcium phosphate plus 800 IU vitamin D3/day; 43% lower hip-fracture count among completers, with similar direction in intention-to-treat analysis. [cal-clin-chapuy1992] Vitamin D3 and calcium to prevent hip fractures in elderly women (1992). https://pubmed.ncbi.nlm.nih.gov/1331788/ DOI: 10.1056/NEJM199212033272305
    Complete structured claim and evidence
  6. Calcium absorption from the tested spinach meal was lower than from milk at equal calcium load.

    Calcium → Intestinal calcium absorption source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    13-adult crossover; 200 mg calcium per test meal, double-isotope measurement.
    exposure
    Mean fractional absorption: spinach 5.1%, milk 27.6%; oxalate slightly exceeded calcium stoichiometrically in tested spinach.
    limitations
    Food-matrix comparison; oxalate binding was inferred from composition, not isolated experimentally. Not a comparison of every plant food.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Equal calcium on a food label need not mean equal absorption.
    primary_references
    [cal-clin-heaney1988] Calcium absorbability from spinach (1988). https://pubmed.ncbi.nlm.nih.gov/3354496/ DOI: 10.1093/ajcn/47.4.707
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1152–1162

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 13-adult crossover; 200 mg calcium per test meal, double-isotope measurement. · source_derived_draft · unverified_draft

    ### cal-food-spinach-absorption Calcium absorption from the tested spinach meal was lower than from milk at equal calcium load. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Equal calcium on a food label need not mean equal absorption. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 13-adult crossover; 200 mg calcium per test meal, double-isotope measurement. limitations: Food-matrix comparison; oxalate binding was inferred from composition, not isolated experimentally. Not a comparison of every plant food. exposure: Mean fractional absorption: spinach 5.1%, milk 27.6%; oxalate slightly exceeded calcium stoichiometrically in tested spinach. [cal-clin-heaney1988] Calcium absorbability from spinach (1988). https://pubmed.ncbi.nlm.nih.gov/3354496/ DOI: 10.1093/ajcn/47.4.707
    Complete structured claim and evidence
  7. One year of calcium supplementation did not significantly alter measured iron-status markers in adolescent girls.

    Calcium → Blood iron-status markers source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    113 girls, randomized double-blind placebo-controlled trial.
    exposure
    500 mg calcium/day with evening meal for one year; reported marker comparisons were nonsignificant.
    limitations
    Does not establish absence of effect in iron-deficient people; hemoglobin, ferritin and soluble transferrin receptor are distinct endpoints.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    No significant worsening of iron markers was found after a year of supplementation in these girls.
    primary_references
    [cal-clin-molgaard2005] Long-term calcium supplementation does not affect the iron status of 12-14-y-old girls (2005). https://pubmed.ncbi.nlm.nih.gov/16002806/ DOI: 10.1093/ajcn.82.1.98
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1434–1444

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 113 girls, randomized double-blind placebo-controlled trial. · source_derived_draft · unverified_draft

    ### cal-iron-status-longterm One year of calcium supplementation did not significantly alter measured iron-status markers in adolescent girls. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: No significant worsening of iron markers was found after a year of supplementation in these girls. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 113 girls, randomized double-blind placebo-controlled trial. limitations: Does not establish absence of effect in iron-deficient people; hemoglobin, ferritin and soluble transferrin receptor are distinct endpoints. exposure: 500 mg calcium/day with evening meal for one year; reported marker comparisons were nonsignificant. [cal-clin-molgaard2005] Long-term calcium supplementation does not affect the iron status of 12-14-y-old girls (2005). https://pubmed.ncbi.nlm.nih.gov/16002806/ DOI: 10.1093/ajcn.82.1.98
    Complete structured claim and evidence
  8. Calcium also reduced heme-iron absorption in the meal experiments.

    Calcium → Heme iron absorption source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Human isotope meal experiments with heme substrate.
    limitations
    A shared mucosal mechanism was proposed, not directly localized to a named protein.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The acute interaction was not limited to nonheme iron.
    primary_references
    [cal-clin-hallberg1991] Calcium: effect of different amounts on nonheme- and heme-iron absorption in humans (1991). https://pubmed.ncbi.nlm.nih.gov/1984335/ DOI: 10.1093/ajcn/53.1.112
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1423–1432

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human isotope meal experiments with heme substrate. · source_derived_draft · unverified_draft

    ### cal-meal-heme-iron Calcium also reduced heme-iron absorption in the meal experiments. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The acute interaction was not limited to nonheme iron. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Human isotope meal experiments with heme substrate. limitations: A shared mucosal mechanism was proposed, not directly localized to a named protein. [cal-clin-hallberg1991] Calcium: effect of different amounts on nonheme- and heme-iron absorption in humans (1991). https://pubmed.ncbi.nlm.nih.gov/1984335/ DOI: 10.1093/ajcn/53.1.112
    Complete structured claim and evidence
  9. Added calcium reduced nonheme-iron absorption in the studied meals.

    Calcium → Nonheme iron absorption source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Human isotope meal experiments.
    limitations
    Meal processing/phytate and direct effects both occurred; no specific molecular transporter was identified and long-term iron deficiency was not demonstrated.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Calcium can reduce iron absorbed from a particular meal.
    primary_references
    [cal-clin-hallberg1991] Calcium: effect of different amounts on nonheme- and heme-iron absorption in humans (1991). https://pubmed.ncbi.nlm.nih.gov/1984335/ DOI: 10.1093/ajcn/53.1.112
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1412–1421

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human isotope meal experiments. · source_derived_draft · unverified_draft

    ### cal-meal-nonheme-iron Added calcium reduced nonheme-iron absorption in the studied meals. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium can reduce iron absorbed from a particular meal. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Human isotope meal experiments. limitations: Meal processing/phytate and direct effects both occurred; no specific molecular transporter was identified and long-term iron deficiency was not demonstrated. [cal-clin-hallberg1991] Calcium: effect of different amounts on nonheme- and heme-iron absorption in humans (1991). https://pubmed.ncbi.nlm.nih.gov/1984335/ DOI: 10.1093/ajcn/53.1.112
    Complete structured claim and evidence
  10. The 500-mg calcium regimen met the prespecified noninferiority criterion versus 1500 mg for preeclampsia in both 2024 trials.

    Calcium → Preeclampsia incidence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Independent India and Tanzania trials; 11,000 nulliparous women each.
    exposure
    500 versus 1500 mg elemental calcium/day; preeclampsia RR noninferiority margin 1.54.
    limitations
    No placebo arm: this cannot establish benefit versus no supplement. Noninferiority is not exact equality or a dosing recommendation.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The lower tested dose performed within the trial margin relative to the higher dose.
    primary_references
    [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1353–1363

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Independent India and Tanzania trials; 11,000 nulliparous women each. · source_derived_draft · unverified_draft

    ### cal-pregnancy-dose-noninferiority The 500-mg calcium regimen met the prespecified noninferiority criterion versus 1500 mg for preeclampsia in both 2024 trials. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The lower tested dose performed within the trial margin relative to the higher dose. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Independent India and Tanzania trials; 11,000 nulliparous women each. limitations: No placebo arm: this cannot establish benefit versus no supplement. Noninferiority is not exact equality or a dosing recommendation. exposure: 500 versus 1500 mg elemental calcium/day; preeclampsia RR noninferiority margin 1.54. [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    Complete structured claim and evidence
  11. The lower calcium regimen met the preterm-live-birth noninferiority criterion in India.

    Calcium → Preterm live birth source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    India component of the two trials.
    exposure
    RR 0.89, 95% CI 0.80-0.98; margin 1.16.
    limitations
    No untreated control; noninferiority need not generalize to another setting.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The India result met the planned comparison threshold.
    primary_references
    [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1365–1375

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · India component of the two trials. · source_derived_draft · unverified_draft

    ### cal-pregnancy-india-preterm The lower calcium regimen met the preterm-live-birth noninferiority criterion in India. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The India result met the planned comparison threshold. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: India component of the two trials. limitations: No untreated control; noninferiority need not generalize to another setting. exposure: RR 0.89, 95% CI 0.80-0.98; margin 1.16. [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    Complete structured claim and evidence
  12. The lower regimen did not meet preterm-live-birth noninferiority in Tanzania.

    Calcium → Preterm live birth source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Tanzania component of the two trials.
    exposure
    RR 1.07, 95% CI 0.95-1.21; margin 1.16.
    limitations
    Failure to establish noninferiority does not prove inferiority or harm.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The Tanzania estimate was too uncertain to meet the same threshold.
    primary_references
    [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1377–1387

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Tanzania component of the two trials. · source_derived_draft · unverified_draft

    ### cal-pregnancy-tanzania-preterm The lower regimen did not meet preterm-live-birth noninferiority in Tanzania. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The Tanzania estimate was too uncertain to meet the same threshold. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Tanzania component of the two trials. limitations: Failure to establish noninferiority does not prove inferiority or harm. exposure: RR 1.07, 95% CI 0.95-1.21; margin 1.16. [cal-clin-dwarkanath2024] Two Randomized Trials of Low-Dose Calcium Supplementation in Pregnancy (2024). https://www.nejm.org/doi/full/10.1056/NEJMoa2307212 DOI: 10.1056/NEJMoa2307212
    Complete structured claim and evidence
  13. Calcium-containing treatment produced more biochemical and radiographic healing than vitamin D alone in the Nigerian rickets trial.

    Calcium → Nutritional rickets healing source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    123 children, 24-week randomized trial; low calcium intake also present in matched controls.
    exposure
    1000 mg elemental calcium/day, vitamin D injections, or both. Combined healing endpoint: calcium 61%, combined 58%, vitamin D 19%. Historical regimens only.
    limitations
    Does not make every case of rickets calcium-deficiency disease. The combined endpoint included alkaline phosphatase and radiographs. The injected vitamin D molecular form is not assigned here.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    In these children, replacing calcium helped heal rickets.
    primary_references
    [cal-clin-thacher1999] A Comparison of Calcium, Vitamin D, or Both for Nutritional Rickets in Nigerian Children (1999). https://www.nejm.org/doi/full/10.1056/NEJM199908193410803 DOI: 10.1056/NEJM199908193410803
    tissue_or_cell_type
    Human clinical or absorption endpoint
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1187–1197

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 123 children, 24-week randomized trial; low calcium intake also present in matched controls. · source_derived_draft · unverified_draft

    ### cal-rickets-repletion Calcium-containing treatment produced more biochemical and radiographic healing than vitamin D alone in the Nigerian rickets trial. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: In these children, replacing calcium helped heal rickets. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 123 children, 24-week randomized trial; low calcium intake also present in matched controls. limitations: Does not make every case of rickets calcium-deficiency disease. The combined endpoint included alkaline phosphatase and radiographs. The injected vitamin D molecular form is not assigned here. exposure: 1000 mg elemental calcium/day, vitamin D injections, or both. Combined healing endpoint: calcium 61%, combined 58%, vitamin D 19%. Historical regimens only. [cal-clin-thacher1999] A Comparison of Calcium, Vitamin D, or Both for Nutritional Rickets in Nigerian Children (1999). https://www.nejm.org/doi/full/10.1056/NEJM199908193410803 DOI: 10.1056/NEJM199908193410803
    Complete structured claim and evidence
  14. WHI found no significant effect of calcium plus vitamin D on myocardial infarction or coronary death.

    Calcium → Myocardial infarction or coronary death source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Prespecified secondary WHI outcome; seven years.
    exposure
    MI/coronary-death HR 1.04, 95% CI 0.92-1.18.
    limitations
    Different cointervention, participants and ascertainment from the calcium-only trial; absence of significance does not prove universal safety.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    This trial did not reproduce a clear increase in coronary events.
    primary_references
    [cal-clin-hsia2007] Calcium/vitamin D supplementation and cardiovascular events (2007). https://pubmed.ncbi.nlm.nih.gov/17309935/ DOI: 10.1161/CIRCULATIONAHA.106.673491
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1293–1303

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Prespecified secondary WHI outcome; seven years. · source_derived_draft · unverified_draft

    ### cal-whi-coronary-events WHI found no significant effect of calcium plus vitamin D on myocardial infarction or coronary death. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: This trial did not reproduce a clear increase in coronary events. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Prespecified secondary WHI outcome; seven years. limitations: Different cointervention, participants and ascertainment from the calcium-only trial; absence of significance does not prove universal safety. exposure: MI/coronary-death HR 1.04, 95% CI 0.92-1.18. [cal-clin-hsia2007] Calcium/vitamin D supplementation and cardiovascular events (2007). https://pubmed.ncbi.nlm.nih.gov/17309935/ DOI: 10.1161/CIRCULATIONAHA.106.673491
    Complete structured claim and evidence
  15. WHI calcium plus vitamin D did not significantly reduce hip fractures in the intention-to-treat analysis.

    Calcium → Hip fracture incidence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    36,282 postmenopausal women; seven-year mean follow-up.
    exposure
    1000 mg elemental calcium as carbonate plus 400 IU vitamin D3/day; hip-fracture HR 0.88, 95% CI 0.72-1.08.
    limitations
    Adherence and background supplement use complicate comparison; a nonsignificant result is not proof of zero effect.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    A larger trial did not establish a hip-fracture benefit for its overall assigned-treatment groups.
    primary_references
    [cal-clin-jackson2006] Calcium plus vitamin D supplementation and the risk of fractures (2006). https://pubmed.ncbi.nlm.nih.gov/16481635/ DOI: 10.1056/NEJMoa055218
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1211–1221

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 36,282 postmenopausal women; seven-year mean follow-up. · source_derived_draft · unverified_draft

    ### cal-whi-hip-fractures WHI calcium plus vitamin D did not significantly reduce hip fractures in the intention-to-treat analysis. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: A larger trial did not establish a hip-fracture benefit for its overall assigned-treatment groups. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 36,282 postmenopausal women; seven-year mean follow-up. limitations: Adherence and background supplement use complicate comparison; a nonsignificant result is not proof of zero effect. exposure: 1000 mg elemental calcium as carbonate plus 400 IU vitamin D3/day; hip-fracture HR 0.88, 95% CI 0.72-1.08. [cal-clin-jackson2006] Calcium plus vitamin D supplementation and the risk of fractures (2006). https://pubmed.ncbi.nlm.nih.gov/16481635/ DOI: 10.1056/NEJMoa055218
    Complete structured claim and evidence
  16. WHI assigned calcium plus vitamin D increased reported renal-calculus events relative to placebo.

    Calcium → Urinary stone incidence source_derived_draftungraded
    Experimental context and source evidence
    experimental_model
    Randomized WHI safety outcome.
    exposure
    Renal-calculus HR 1.17, 95% CI 1.02-1.34; same assigned regimen as the fracture analysis.
    limitations
    Combined intervention; cannot attribute the whole effect to calcium or identify every stone composition.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The same trial recorded more kidney-stone events with the combined supplements.
    primary_references
    [cal-clin-jackson2006] Calcium plus vitamin D supplementation and the risk of fractures (2006). https://pubmed.ncbi.nlm.nih.gov/16481635/ DOI: 10.1056/NEJMoa055218
    tissue_or_cell_type
    Human clinical or absorption endpoint

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1223–1233

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized WHI safety outcome. · source_derived_draft · unverified_draft

    ### cal-whi-urinary-stones WHI assigned calcium plus vitamin D increased reported renal-calculus events relative to placebo. Condition category: normal nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The same trial recorded more kidney-stone events with the combined supplements. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Randomized WHI safety outcome. limitations: Combined intervention; cannot attribute the whole effect to calcium or identify every stone composition. exposure: Renal-calculus HR 1.17, 95% CI 1.02-1.34; same assigned regimen as the fracture analysis. [cal-clin-jackson2006] Calcium plus vitamin D supplementation and the risk of fractures (2006). https://pubmed.ncbi.nlm.nih.gov/16481635/ DOI: 10.1056/NEJMoa055218
    Complete structured claim and evidence
  17. Eclampsia was less frequent with calcium in a secondary analysis of the same WHO trial.

    Calcium → Eclampsia incidence source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    Same randomized pregnancy trial.
    exposure
    Eclampsia RR 0.68, 95% CI 0.48-0.97.
    limitations
    Secondary endpoint; distinct from preeclampsia incidence and not proof of an identified molecular mediator.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    A severe secondary outcome improved despite the null primary result.
    primary_references
    [cal-clin-villar2006] World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women (2006). https://pubmed.ncbi.nlm.nih.gov/16522392/ DOI: 10.1016/j.ajog.2006.01.068
    tissue_or_cell_type
    Human clinical or absorption endpoint
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1341–1351

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Same randomized pregnancy trial. · source_derived_draft · unverified_draft

    ### cal-who-eclampsia Eclampsia was less frequent with calcium in a secondary analysis of the same WHO trial. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: A severe secondary outcome improved despite the null primary result. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: Same randomized pregnancy trial. limitations: Secondary endpoint; distinct from preeclampsia incidence and not proof of an identified molecular mediator. exposure: Eclampsia RR 0.68, 95% CI 0.48-0.97. [cal-clin-villar2006] World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women (2006). https://pubmed.ncbi.nlm.nih.gov/16522392/ DOI: 10.1016/j.ajog.2006.01.068
    Complete structured claim and evidence
  18. In the WHO low-intake pregnancy trial, calcium did not significantly reduce overall preeclampsia incidence.

    Calcium → Preeclampsia incidence source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    8325 nulliparous women; blinded placebo comparison.
    exposure
    1.5 g calcium/day starting before 20 weeks; preeclampsia 4.1% versus 4.5%.
    limitations
    Preeclampsia was primary; reported benefits on severe outcomes were secondary.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Low baseline intake did not guarantee a benefit on the primary pregnancy outcome.
    primary_references
    [cal-clin-villar2006] World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women (2006). https://pubmed.ncbi.nlm.nih.gov/16522392/ DOI: 10.1016/j.ajog.2006.01.068
    tissue_or_cell_type
    Human clinical or absorption endpoint
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1329–1339

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 8325 nulliparous women; blinded placebo comparison. · source_derived_draft · unverified_draft

    ### cal-who-preeclampsia In the WHO low-intake pregnancy trial, calcium did not significantly reduce overall preeclampsia incidence. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Low baseline intake did not guarantee a benefit on the primary pregnancy outcome. organism: Homo sapiens tissue_or_cell_type: Human clinical or absorption endpoint experimental_model: 8325 nulliparous women; blinded placebo comparison. limitations: Preeclampsia was primary; reported benefits on severe outcomes were secondary. exposure: 1.5 g calcium/day starting before 20 weeks; preeclampsia 4.1% versus 4.5%. [cal-clin-villar2006] World Health Organization randomized trial of calcium supplementation among low calcium intake pregnant women (2006). https://pubmed.ncbi.nlm.nih.gov/16522392/ DOI: 10.1016/j.ajog.2006.01.068
    Complete structured claim and evidence
  19. A calcium-deficient diet increased osteoclasts and bone loss in adult mice; osteocyte-directed Rankl deletion blunted the response.

    Calcium → Osteoclastic bone resorption source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    30 days of 0.01% versus 0.516% dietary calcium
    limitations
    Mouse diet and Cre-targeting scope limit human generalization; bone loss was blunted, not necessarily abolished.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Mus musculus
    plain_language
    When dietary calcium was severely restricted, osteocyte RANKL helped drive withdrawal from bone.
    primary_references
    [xiong2014] Osteocyte-derived RANKL is a critical mediator of the increased bone resorption caused by dietary calcium deficiency (2014). https://pmc.ncbi.nlm.nih.gov/articles/PMC4125539/ DOI: 10.1016/j.bone.2014.06.006
    tissue_or_cell_type
    Adult cortical and cancellous bone
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 1070–1079

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 30 days of 0.01% versus 0.516% dietary calcium · source_derived_draft · unverified_draft

    ### low-calcium-diet-osteocyte-rankl-resorption A calcium-deficient diet increased osteoclasts and bone loss in adult mice; osteocyte-directed Rankl deletion blunted the response. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: When dietary calcium was severely restricted, osteocyte RANKL helped drive withdrawal from bone. organism: Mus musculus tissue_or_cell_type: Adult cortical and cancellous bone experimental_model: 30 days of 0.01% versus 0.516% dietary calcium limitations: Mouse diet and Cre-targeting scope limit human generalization; bone loss was blunted, not necessarily abolished. [xiong2014] Osteocyte-derived RANKL is a critical mediator of the increased bone resorption caused by dietary calcium deficiency (2014). https://pmc.ncbi.nlm.nih.gov/articles/PMC4125539/ DOI: 10.1016/j.bone.2014.06.006
    Complete structured claim and evidence
  20. The same diet reduction increased fractional oral 47Ca retention within one week.

    Calcium → Fractional whole-body calcium retention source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention
    limitations
    Retention indexes absorption; greater fraction does not guarantee adequate absolute uptake.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    The retained fraction adapts to low intake.
    primary_references
    [dawsonhughes1988] Effect of lowering dietary calcium intake on fractional whole body calcium retention (1988). https://pubmed.ncbi.nlm.nih.gov/3132484/ DOI: 10.1210/jcem-67-1-62
    tissue_or_cell_type
    Whole body
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 302–311

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention · source_derived_draft · unverified_draft

    ### low-calcium-intake-fractional-retention The same diet reduction increased fractional oral 47Ca retention within one week. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The retained fraction adapts to low intake. organism: Homo sapiens tissue_or_cell_type: Whole body experimental_model: Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention limitations: Retention indexes absorption; greater fraction does not guarantee adequate absolute uptake. [dawsonhughes1988] Effect of lowering dietary calcium intake on fractional whole body calcium retention (1988). https://pubmed.ncbi.nlm.nih.gov/3132484/ DOI: 10.1210/jcem-67-1-62
    Complete structured claim and evidence
  21. Reducing calcium intake from 2000 to 300 mg/day increased intact PTH within one week in nine healthy women.

    Calcium → Serum PTH concentration source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    experimental_model
    Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention
    limitations
    Small controlled study; low intake is not proof of symptomatic deficiency.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Homo sapiens
    plain_language
    Low intake recruits a hormonal response.
    primary_references
    [dawsonhughes1988] Effect of lowering dietary calcium intake on fractional whole body calcium retention (1988). https://pubmed.ncbi.nlm.nih.gov/3132484/ DOI: 10.1210/jcem-67-1-62
    tissue_or_cell_type
    Blood
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 291–300

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention · source_derived_draft · unverified_draft

    ### low-calcium-intake-increases-pth Reducing calcium intake from 2000 to 300 mg/day increased intact PTH within one week in nine healthy women. Condition category: nutrient_deficiency nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Low intake recruits a hormonal response. organism: Homo sapiens tissue_or_cell_type: Blood experimental_model: Nine healthy women; controlled 2000-to-300 mg/day calcium diet change and oral 47Ca retention limitations: Small controlled study; low intake is not proof of symptomatic deficiency. [dawsonhughes1988] Effect of lowering dietary calcium intake on fractional whole body calcium retention (1988). https://pubmed.ncbi.nlm.nih.gov/3132484/ DOI: 10.1210/jcem-67-1-62
    Complete structured claim and evidence
  22. A mineral/lactose rescue diet normalizes ionized calcium in VDR-ablated mice.

    Calcium → Serum ionized calcium concentration source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    experimental_model
    VDR-ablated mice and controls fed a mineral/lactose rescue diet
    limitations
    Combined dietary intervention; cannot attribute rescue to calcium alone.
    nutrient_topic
    Calcium research collection; topical membership is not evidence of a direct dietary effect. · Calcium
    organism
    Mus musculus
    plain_language
    Dietary mineral delivery can bypass part of receptor failure.
    primary_references
    [li1998] Normalization of mineral ion homeostasis by dietary means prevents hyperparathyroidism, rickets, and osteomalacia, but not alopecia in vitamin D receptor-ablated mice (1998). https://pubmed.ncbi.nlm.nih.gov/9751523/ DOI: 10.1210/endo.139.10.6262
    reported_effect
    normalizing
    tissue_or_cell_type
    Intestine and blood
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Calcium: mechanism-first literature curation (2026-09-17) · lines 146–156

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · VDR-ablated mice and controls fed a mineral/lactose rescue diet · source_derived_draft · unverified_draft

    ### vdr-null-mineral-diet-rescue A mineral/lactose rescue diet normalizes ionized calcium in VDR-ablated mice. Condition category: machinery_impairment nutrient_topic: Calcium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Dietary mineral delivery can bypass part of receptor failure. organism: Mus musculus tissue_or_cell_type: Intestine and blood experimental_model: VDR-ablated mice and controls fed a mineral/lactose rescue diet limitations: Combined dietary intervention; cannot attribute rescue to calcium alone. reported_effect: normalizing [li1998] Normalization of mineral ion homeostasis by dietary means prevents hyperparathyroidism, rickets, and osteomalacia, but not alopecia in vitamin D receptor-ablated mice (1998). https://pubmed.ncbi.nlm.nih.gov/9751523/ DOI: 10.1210/endo.139.10.6262
    Complete structured claim and evidence
  23. In the comparative diabetes study, adding oral calcium after three months of metformin reversed the decline in serum holo-transcobalamin.

    Calcium → Serum holotranscobalamin concentration source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    true
    experimental_model
    21 adults with type 2 diabetes; 14 switched to metformin, then received calcium
    exposure
    Oral calcium after three months of metformin; dose not specified in inspected abstract
    limitations
    Small sequential comparative intervention. Serum holo-TC is an indirect absorption readout and does not directly prove membrane calcium antagonism.
    nutrient_topic
    Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B12 (cobalamins)
    organism
    Homo sapiens
    plain_language
    Calcium increased the circulating B12-carrier marker after metformin.
    primary_references
    [bauman-2000-calcium] Increased intake of calcium reverses vitamin B12 malabsorption induced by metformin. (2000). https://pubmed.ncbi.nlm.nih.gov/10977010/ DOI: 10.2337/diacare.23.9.1227
    tissue_or_cell_type
    Circulating holo-transcobalamin

    Vitamin B12: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 439–450

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 21 adults with type 2 diabetes; 14 switched to metformin, then received calcium · source_derived_draft · unverified_draft

    ### b12-abs-bauman-calcium-holotc In the comparative diabetes study, adding oral calcium after three months of metformin reversed the decline in serum holo-transcobalamin. Condition category: normal nutrient_topic: Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium increased the circulating B12-carrier marker after metformin. organism: Homo sapiens tissue_or_cell_type: Circulating holo-transcobalamin experimental_model: 21 adults with type 2 diabetes; 14 switched to metformin, then received calcium limitations: Small sequential comparative intervention. Serum holo-TC is an indirect absorption readout and does not directly prove membrane calcium antagonism. exposure: Oral calcium after three months of metformin; dose not specified in inspected abstract cross_nutrient: true [bauman-2000-calcium] Increased intake of calcium reverses vitamin B12 malabsorption induced by metformin. (2000). https://pubmed.ncbi.nlm.nih.gov/10977010/ DOI: 10.2337/diacare.23.9.1227
    Complete structured claim and evidence
  24. Adding calcium 500 mg to metformin 850 mg raised mean tracer bioavailability from 30.8% to 46.4% in seven healthy completers (p=0.003).

    Experimental context and source evidence
    cross_nutrient
    true
    experimental_model
    Seven healthy adult completers; three experimental days separated by one-month washouts
    exposure
    Metformin 850 mg plus calcium 500 mg and carbon-13 cyanocobalamin
    limitations
    Small acute tracer pilot in healthy adults; cannot establish prevention of chronic deficiency or identify the exact molecular metformin target. Doses describe the experiment, not advice.
    nutrient_topic
    Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin B12 (cobalamins)
    organism
    Homo sapiens
    plain_language
    Calcium coadministration reversed the tracer reduction in this pilot.
    primary_references
    [muralidharan-2024-calcium] Effect of calcium supplementation on reversing metformin-based inhibition of vitamin B12 bioavailability in healthy adults using a [13C] cyanocobalamin tracer - A pilot study. (2024). https://pubmed.ncbi.nlm.nih.gov/38901951/ DOI: 10.1016/j.clnesp.2024.04.024
    tissue_or_cell_type
    Intestinal absorption assessed from serial venous tracer measurements

    Vitamin B12: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 465–476

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Seven healthy adult completers; three experimental days separated by one-month washouts · source_derived_draft · unverified_draft

    ### b12-abs-calcium-tracer-rescue Adding calcium 500 mg to metformin 850 mg raised mean tracer bioavailability from 30.8% to 46.4% in seven healthy completers (p=0.003). Condition category: normal nutrient_topic: Vitamin B12 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium coadministration reversed the tracer reduction in this pilot. organism: Homo sapiens tissue_or_cell_type: Intestinal absorption assessed from serial venous tracer measurements experimental_model: Seven healthy adult completers; three experimental days separated by one-month washouts limitations: Small acute tracer pilot in healthy adults; cannot establish prevention of chronic deficiency or identify the exact molecular metformin target. Doses describe the experiment, not advice. exposure: Metformin 850 mg plus calcium 500 mg and carbon-13 cyanocobalamin cross_nutrient: true [muralidharan-2024-calcium] Effect of calcium supplementation on reversing metformin-based inhibition of vitamin B12 bioavailability in healthy adults using a [13C] cyanocobalamin tracer - A pilot study. (2024). https://pubmed.ncbi.nlm.nih.gov/38901951/ DOI: 10.1016/j.clnesp.2024.04.024
    Complete structured claim and evidence
  25. Adding calcium to the human-milk test meal reduced manganese absorption in adults.

    Calcium → Intestinal manganese absorption source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Manganese (absorbed_nutrient)
    evidence_span
    {"source_cache": "artifacts/manganese-clinical-sources/davidsson1991.abstract.txt", "locator": "Indexed primary abstract", "file_sha256": "7570e2285532eac2292b252a3813f1be97b46d68529a4d4150a88b4f9038676a", "start_char": 0, "end_char": 912, "text_sha256": "7570e2285532eac2292b252a3813f1be97b46d68529a4d4150a88b4f9038676a", "text_characters": 912}
    experimental_model
    Paired radiotracer test-meal study in adults
    exposure
    Human milk, infant formula and wheat bread used as adult test meals; individual mineral and dietary-component additions.
    limitations
    These were adult experiments even when milk or infant formula was the matrix. Added amounts were not independently verified from the indexed abstract; no universal interaction or spacing rule follows.
    nutrient_topic
    Manganese research collection; topical membership is not evidence of a direct dietary effect. · Manganese
    organism
    Homo sapiens
    plain_language
    Calcium changed manganese uptake in this particular meal.
    primary_references
    [mn-clin-davidsson1991] The effect of individual dietary components on manganese absorption in humans. (1991). https://pubmed.ncbi.nlm.nih.gov/1957822/ DOI: 10.1093/ajcn/54.6.1065
    tissue_or_cell_type
    Intestinal absorption

    Manganese: enzyme cofactors, glycosylation, transport and nutrient interactions (2026-09-17) · lines 1020–1032

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Paired radiotracer test-meal study in adults · source_derived_draft · unverified_draft

    ### mn-clin-meal-calcium Adding calcium to the human-milk test meal reduced manganese absorption in adults. Condition category: normal nutrient_topic: Manganese research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium changed manganese uptake in this particular meal. organism: Homo sapiens tissue_or_cell_type: Intestinal absorption experimental_model: Paired radiotracer test-meal study in adults limitations: These were adult experiments even when milk or infant formula was the matrix. Added amounts were not independently verified from the indexed abstract; no universal interaction or spacing rule follows. exposure: Human milk, infant formula and wheat bread used as adult test meals; individual mineral and dietary-component additions. cross_nutrient: Manganese (absorbed_nutrient) evidence_span: {"source_cache": "artifacts/manganese-clinical-sources/davidsson1991.abstract.txt", "locator": "Indexed primary abstract", "file_sha256": "7570e2285532eac2292b252a3813f1be97b46d68529a4d4150a88b4f9038676a", "start_char": 0, "end_char": 912, "text_sha256": "7570e2285532eac2292b252a3813f1be97b46d68529a4d4150a88b4f9038676a", "text_characters": 912} [mn-clin-davidsson1991] The effect of individual dietary components on manganese absorption in humans. (1991). https://pubmed.ncbi.nlm.nih.gov/1957822/ DOI: 10.1093/ajcn/54.6.1065
    Complete structured claim and evidence

Where it participates (unsigned role)

  1. The studied Vitros 5600 PTH assay fell by a mean 61% after biotin, while serum calcium remained stable.

    Biotin → Ortho Vitros 5600 PTH immunoassay result source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    biomarker_context Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/biotin-research/28973622.fulltext.txt", "locator": "Exact primary full-text span; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ee7e5947d8391b7a0fa7601d8390147b99c5ff603b3462e9d1aa7f3db42b915", "start_char": 20261, "end_char": 20798, "text_sha256": "440bd38aad94623f97cd7f956c63815b7a25d790328c4407bcdf6d24f8d2be0d"}
    experimental_model
    Nonrandomized crossover study of 6 healthy adults, 37 assays and 11 analytes
    exposure
    10 mg oral biotin daily for 7 days
    limitations
    Interference depends on assay architecture and version; this study does not establish current platform performance, a universal washout time or true hormone changes.
    nutrient_topic
    Biotin research collection; topical membership is not evidence of a direct dietary effect. · Biotin
    organism
    Homo sapiens
    plain_language
    A falsely low PTH result can misleadingly suggest a problem in calcium regulation.
    primary_references
    [b7-p28973622] Association of Biotin Ingestion With Performance of Hormone and Nonhormone Assays in Healthy Adults. (2017). https://pubmed.ncbi.nlm.nih.gov/28973622/ DOI: 10.1001/jama.2017.13705
    tissue_or_cell_type
    Blood specimens measured on named 2017 assay systems
    trigger_kind
    biomarker_context Imported condition classification; unverified.

    Biotin: carboxylases, recycling, deficiency and nutrient interactions (2026-09-17) · lines 1261–1272

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Nonrandomized crossover study of 6 healthy adults, 37 assays and 11 analytes · source_derived_draft · unverified_draft

    ### b7-assay-pth The studied Vitros 5600 PTH assay fell by a mean 61% after biotin, while serum calcium remained stable. Condition category: biomarker_context nutrient_topic: Biotin research collection; topical membership is not evidence of a direct dietary effect. plain_language: A falsely low PTH result can misleadingly suggest a problem in calcium regulation. organism: Homo sapiens tissue_or_cell_type: Blood specimens measured on named 2017 assay systems experimental_model: Nonrandomized crossover study of 6 healthy adults, 37 assays and 11 analytes limitations: Interference depends on assay architecture and version; this study does not establish current platform performance, a universal washout time or true hormone changes. exposure: 10 mg oral biotin daily for 7 days evidence_span: {"source_cache": "artifacts/biotin-research/28973622.fulltext.txt", "locator": "Exact primary full-text span; zero-based, end-exclusive Unicode character offsets", "file_sha256": "4ee7e5947d8391b7a0fa7601d8390147b99c5ff603b3462e9d1aa7f3db42b915", "start_char": 20261, "end_char": 20798, "text_sha256": "440bd38aad94623f97cd7f956c63815b7a25d790328c4407bcdf6d24f8d2be0d"} [b7-p28973622] Association of Biotin Ingestion With Performance of Hormone and Nonhormone Assays in Healthy Adults. (2017). https://pubmed.ncbi.nlm.nih.gov/28973622/ DOI: 10.1001/jama.2017.13705
    Complete structured claim and evidence
  2. High-dose supplemental zinc reduced measured Mg absorption in the pooled metabolic-balance groups.

    Zinc sulfate → Intestinal magnesium absorption source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Zinc -> magnesium availability; calcium intake recorded as context.
    experimental_model
    Adult men; three dietary calcium strata.
    exposure
    142 mg Zn/day as sulfate; calcium 230, 500 or 800 mg/day. Only the 500-mg stratum individually significant; pooled groups significant.
    limitations
    142 mg zinc/day is a high experimental exposure; ordinary food zinc effects and a shared transporter were not established.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Homo sapiens
    plain_language
    Large zinc exposure can interfere with magnesium uptake.
    primary_references
    [mg-spencer1994] Inhibitory effects of zinc on magnesium balance and magnesium absorption in man (1994). https://pubmed.ncbi.nlm.nih.gov/7836627/ DOI: 10.1080/07315724.1994.10718438
    tissue_or_cell_type
    Human intestinal absorption and metabolic balance

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 1577–1588

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Adult men; three dietary calcium strata. · source_derived_draft · unverified_draft

    ### mg-high-zinc-lowers-absorption High-dose supplemental zinc reduced measured Mg absorption in the pooled metabolic-balance groups. Condition category: normal nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Large zinc exposure can interfere with magnesium uptake. organism: Homo sapiens tissue_or_cell_type: Human intestinal absorption and metabolic balance experimental_model: Adult men; three dietary calcium strata. limitations: 142 mg zinc/day is a high experimental exposure; ordinary food zinc effects and a shared transporter were not established. cross_nutrient: Zinc -> magnesium availability; calcium intake recorded as context. exposure: 142 mg Zn/day as sulfate; calcium 230, 500 or 800 mg/day. Only the 500-mg stratum individually significant; pooled groups significant. [mg-spencer1994] Inhibitory effects of zinc on magnesium balance and magnesium absorption in man (1994). https://pubmed.ncbi.nlm.nih.gov/7836627/ DOI: 10.1080/07315724.1994.10718438
    Complete structured claim and evidence
  3. Recombinant human PHOSPHO1 showed strong Mg dependence when hydrolyzing phosphoethanolamine and phosphocholine.

    Experimental context and source evidence
    cross_nutrient
    Magnesium -> PHOSPHO1 -> phosphate production; joins the existing calcium PHOSPHO1 records.
    experimental_model
    Purified recombinant phosphatase assays.
    limitations
    Enzyme evidence does not measure the effect of oral Mg on bone; substrate Km values are not Mg deficiency thresholds.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Homo sapiens
    plain_language
    Magnesium helps a phosphate-releasing enzyme already connected to calcium mineralization.
    primary_references
    [mg-roberts2004] Human PHOSPHO1 exhibits high specific phosphoethanolamine and phosphocholine phosphatase activities (2004). https://pubmed.ncbi.nlm.nih.gov/15175005/ DOI: 10.1042/bj20040511
    tissue_or_cell_type
    Purified recombinant human PHOSPHO1

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 1455–1465

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Purified recombinant phosphatase assays. · source_derived_draft · unverified_draft

    ### mg-phospho1-cofactor Recombinant human PHOSPHO1 showed strong Mg dependence when hydrolyzing phosphoethanolamine and phosphocholine. Condition category: normal nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Magnesium helps a phosphate-releasing enzyme already connected to calcium mineralization. organism: Homo sapiens tissue_or_cell_type: Purified recombinant human PHOSPHO1 experimental_model: Purified recombinant phosphatase assays. limitations: Enzyme evidence does not measure the effect of oral Mg on bone; substrate Km values are not Mg deficiency thresholds. cross_nutrient: Magnesium -> PHOSPHO1 -> phosphate production; joins the existing calcium PHOSPHO1 records. [mg-roberts2004] Human PHOSPHO1 exhibits high specific phosphoethanolamine and phosphocholine phosphatase activities (2004). https://pubmed.ncbi.nlm.nih.gov/15175005/ DOI: 10.1042/bj20040511
    Complete structured claim and evidence
  4. Magnesium assignment altered plasma 25(OH)D3 differently by baseline vitamin D: an increase near 30 ng/mL and a decrease at higher baseline concentrations.

    Magnesium → Plasma calcifediol concentration source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Magnesium <-> vitamin D status; baseline-dependent clinical endpoint.
    experimental_model
    Randomized 12-week ancillary analysis, 180 adults.
    exposure
    Personalized Mg supplementation; baseline calcium:magnesium intake ratio at least 2.6. Ratios describe enrollment, not a recommended target.
    limitations
    Only two participants had overt vitamin D deficiency; the trial does not show universal deficiency rescue or identify the responsible enzyme.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Homo sapiens
    plain_language
    The vitamin D response depended on the starting level.
    primary_references
    [mg-dai2018] Magnesium status and supplementation influence vitamin D status and metabolism: results from a randomized trial (2018). https://pubmed.ncbi.nlm.nih.gov/30541089/ DOI: 10.1093/ajcn/nqy274
    tissue_or_cell_type
    Human plasma

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 1430–1441

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized 12-week ancillary analysis, 180 adults. · source_derived_draft · unverified_draft

    ### mg-supplement-calcifediol-baseline-dependent Magnesium assignment altered plasma 25(OH)D3 differently by baseline vitamin D: an increase near 30 ng/mL and a decrease at higher baseline concentrations. Condition category: normal nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: The vitamin D response depended on the starting level. organism: Homo sapiens tissue_or_cell_type: Human plasma experimental_model: Randomized 12-week ancillary analysis, 180 adults. limitations: Only two participants had overt vitamin D deficiency; the trial does not show universal deficiency rescue or identify the responsible enzyme. cross_nutrient: Magnesium <-> vitamin D status; baseline-dependent clinical endpoint. exposure: Personalized Mg supplementation; baseline calcium:magnesium intake ratio at least 2.6. Ratios describe enrollment, not a recommended target. [mg-dai2018] Magnesium status and supplementation influence vitamin D status and metabolism: results from a randomized trial (2018). https://pubmed.ncbi.nlm.nih.gov/30541089/ DOI: 10.1093/ajcn/nqy274
    Complete structured claim and evidence
  5. Three weeks of selective Mg depletion produced a small but significant reduction in serum calcium in the adult study.

    Magnesium → Serum calcium concentration source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    cross_nutrient
    magnesium -> calcium
    experimental_model
    26 initially normal adults before/after three-week low-Mg diet
    limitations
    Mean change in a small controlled study; not evidence that every mildly low Mg value causes clinical hypocalcemia.
    nutrient_topic
    Magnesium research collection; topical membership is not evidence of a direct dietary effect. · Magnesium
    organism
    Homo sapiens
    plain_language
    Calcium regulation changed during experimental Mg shortage even without a preceding calcium-repletion failure.
    primary_references
    [fatemi-1991-selective-depletion] Effect of experimental human magnesium depletion on parathyroid hormone secretion and 1,25-dihydroxyvitamin D metabolism. (1991). https://pubmed.ncbi.nlm.nih.gov/1939521/ DOI: 10.1210/jcem-73-5-1067
    tissue_or_cell_type
    Blood; parathyroid and renal mineral axis
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Magnesium: cross-nutrient mechanisms and deficiency (2026-09-17) · lines 373–383

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 26 initially normal adults before/after three-week low-Mg diet · source_derived_draft · unverified_draft

    ### selective-mg-depletion-lowers-circulating-calcium Three weeks of selective Mg depletion produced a small but significant reduction in serum calcium in the adult study. Condition category: nutrient_deficiency nutrient_topic: Magnesium research collection; topical membership is not evidence of a direct dietary effect. plain_language: Calcium regulation changed during experimental Mg shortage even without a preceding calcium-repletion failure. organism: Homo sapiens tissue_or_cell_type: Blood; parathyroid and renal mineral axis experimental_model: 26 initially normal adults before/after three-week low-Mg diet limitations: Mean change in a small controlled study; not evidence that every mildly low Mg value causes clinical hypocalcemia. cross_nutrient: magnesium -> calcium [fatemi-1991-selective-depletion] Effect of experimental human magnesium depletion on parathyroid hormone secretion and 1,25-dihydroxyvitamin D metabolism. (1991). https://pubmed.ncbi.nlm.nih.gov/1939521/ DOI: 10.1210/jcem-73-5-1067
    Complete structured claim and evidence
  6. A non-enteric capsaicin/green-tea/caffeine/tyrosine/calcium mixture increased 24-hour energy expenditure by 160 kJ/day versus placebo; the enteric version did not.

    Experimental context and source evidence
    dose
    Seven days of simple, enteric-coated or placebo preparation
    duration
    7 days
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    evidence_scope
    literature_reviewed; model-specific source-derived curation
    experimental_model
    Nineteen overweight or obese men in a randomized three-way crossover trial
    limitations
    This is a mixture and formulation result, not an isolated-capsaicin estimate; the simple-versus-enteric comparison was P=0.09.
    nutrient_topic
    Capsaicin chapter; interacting nutrients, drugs, peptides and proteins retain their experimental settings. · Capsaicin
    organism
    Nineteen overweight or obese men in a randomized three-way crossover trial
    plain_language
    A non-enteric capsaicin/green-tea/caffeine/tyrosine/calcium mixture increased 24-hour energy expenditure by 160 kJ/day versus placebo; the enteric version did not.
    primary_references
    Bioactive food stimulants of sympathetic activity: effect on 24-h energy expenditure and fat oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15870822/ DOI: 10.1038/sj.ejcn.1602121
    route
    Oral multi-ingredient supplement
    tissue
    Respiration-chamber energy expenditure

    Capsaicin: mechanism of action and interactions (2026-09-20) · lines 132–141

    Original AI-assisted source-specific curation with primary-study citations, model, exposure, route, duration, negative findings and limitations preserved. Not publisher full text. · supports · Nineteen overweight or obese men in a randomized three-way crossover trial · source_derived_draft · unverified_draft

    ## capsaicin-multi-ingredient-energy A non-enteric capsaicin/green-tea/caffeine/tyrosine/calcium mixture increased 24-hour energy expenditure by 160 kJ/day versus placebo; the enteric version did not. Model/species: Nineteen overweight or obese men in a randomized three-way crossover trial Tissue/system: Respiration-chamber energy expenditure Exposure: Seven days of simple, enteric-coated or placebo preparation Route: Oral multi-ingredient supplement Duration: 7 days Limits: This is a mixture and formulation result, not an isolated-capsaicin estimate; the simple-versus-enteric comparison was P=0.09. Primary reference: Bioactive food stimulants of sympathetic activity: effect on 24-h energy expenditure and fat oxidation. (2005). https://pubmed.ncbi.nlm.nih.gov/15870822/ DOI: 10.1038/sj.ejcn.1602121 Access: Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    Complete structured claim and evidence
  7. Adding menatetrenone to calcium did not significantly reduce new vertebral fractures in the full analysis set; the clinical-fracture secondary difference was also nonsignificant.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/k2-research/19082528.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6d29b8f43348d8acd6ee85d4f65bb0cdd1352dd6f5113f58d7e58d7196bd96f5", "start_char": 0, "end_char": 1657, "text_sha256": "6d29b8f43348d8acd6ee85d4f65bb0cdd1352dd6f5113f58d7e58d7196bd96f5"}
    experimental_model
    Randomized open-label trial with blinded endpoint evaluation
    exposure
    Calcium alone versus calcium plus menatetrenone; 36-month primary and 48-month secondary endpoints
    limitations
    Full-analysis null result; advanced-osteoporosis subgroup signals are exploratory and do not replace the overall endpoint.
    nutrient_topic
    Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin K2 / menaquinone family
    organism
    4378 osteoporotic postmenopausal women
    plain_language
    A large trial did not establish a general fracture-prevention benefit from adding MK-4.
    primary_references
    [k2-p19082528] Randomized controlled study on the prevention of osteoporotic fractures (OF study): a phase IV clinical study of 15-mg menatetrenone capsules. (2009). https://pubmed.ncbi.nlm.nih.gov/19082528/ DOI: 10.1007/s00774-008-0008-8
    tissue_or_cell_type
    Vertebral and clinical fractures

    Vitamin K2: menaquinone forms, carboxylation, recycling and nutrient interactions (2026-09-17) · lines 1111–1122

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized open-label trial with blinded endpoint evaluation · source_derived_draft · unverified_draft

    ### k2-mk4-fractures-null Adding menatetrenone to calcium did not significantly reduce new vertebral fractures in the full analysis set; the clinical-fracture secondary difference was also nonsignificant. Condition category: normal nutrient_topic: Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. plain_language: A large trial did not establish a general fracture-prevention benefit from adding MK-4. organism: 4378 osteoporotic postmenopausal women tissue_or_cell_type: Vertebral and clinical fractures experimental_model: Randomized open-label trial with blinded endpoint evaluation limitations: Full-analysis null result; advanced-osteoporosis subgroup signals are exploratory and do not replace the overall endpoint. exposure: Calcium alone versus calcium plus menatetrenone; 36-month primary and 48-month secondary endpoints evidence_span: {"source_cache": "artifacts/k2-research/19082528.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "6d29b8f43348d8acd6ee85d4f65bb0cdd1352dd6f5113f58d7e58d7196bd96f5", "start_char": 0, "end_char": 1657, "text_sha256": "6d29b8f43348d8acd6ee85d4f65bb0cdd1352dd6f5113f58d7e58d7196bd96f5"} [k2-p19082528] Randomized controlled study on the prevention of osteoporotic fractures (OF study): a phase IV clinical study of 15-mg menatetrenone capsules. (2009). https://pubmed.ncbi.nlm.nih.gov/19082528/ DOI: 10.1007/s00774-008-0008-8
    Complete structured claim and evidence
  8. After three years, BMD declined without significant between-group differences, and microarchitecture and turnover changes were also similar.

    Menaquinone-7 / MK-7 → Bone mineral density source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/k2-research/33030563.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138", "start_char": 0, "end_char": 2370, "text_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138"}
    experimental_model
    Three-year double-blind randomized add-on trial
    exposure
    MK-7 375 micrograms/day versus placebo; both groups D3 38 micrograms/day and calcium 800 mg/day
    limitations
    Different population, dose and background supplementation from the 180-microgram trial; the one-year and three-year reports are not independent cohorts.
    nutrient_topic
    Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin K2 / menaquinone family
    organism
    142 postmenopausal women with osteopenia
    plain_language
    Improved carboxylation did not translate into a demonstrated bone-density benefit in this trial.
    primary_references
    [k2-p33030563] The effect of vitamin MK-7 on bone mineral density and microarchitecture in postmenopausal women with osteopenia, a 3-year randomized, placebo-controlled clinical trial. (2021). https://pubmed.ncbi.nlm.nih.gov/33030563/ DOI: 10.1007/s00198-020-05638-z
    tissue_or_cell_type
    Osteocalcin, DXA and bone microarchitecture

    Vitamin K2: menaquinone forms, carboxylation, recycling and nutrient interactions (2026-09-17) · lines 1098–1109

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Three-year double-blind randomized add-on trial · source_derived_draft · unverified_draft

    ### k2-mk7-cad-bone-null After three years, BMD declined without significant between-group differences, and microarchitecture and turnover changes were also similar. Condition category: normal nutrient_topic: Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Improved carboxylation did not translate into a demonstrated bone-density benefit in this trial. organism: 142 postmenopausal women with osteopenia tissue_or_cell_type: Osteocalcin, DXA and bone microarchitecture experimental_model: Three-year double-blind randomized add-on trial limitations: Different population, dose and background supplementation from the 180-microgram trial; the one-year and three-year reports are not independent cohorts. exposure: MK-7 375 micrograms/day versus placebo; both groups D3 38 micrograms/day and calcium 800 mg/day evidence_span: {"source_cache": "artifacts/k2-research/33030563.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138", "start_char": 0, "end_char": 2370, "text_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138"} [k2-p33030563] The effect of vitamin MK-7 on bone mineral density and microarchitecture in postmenopausal women with osteopenia, a 3-year randomized, placebo-controlled clinical trial. (2021). https://pubmed.ncbi.nlm.nih.gov/33030563/ DOI: 10.1007/s00198-020-05638-z
    Complete structured claim and evidence
  9. With calcium and D3 in both groups, MK-7 reduced ucOC by about 65% after one year.

    Menaquinone-7 / MK-7 → Undercarboxylated osteocalcin source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/k2-research/33030563.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138", "start_char": 0, "end_char": 2370, "text_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138"}
    experimental_model
    Three-year double-blind randomized add-on trial
    exposure
    MK-7 375 micrograms/day versus placebo; both groups D3 38 micrograms/day and calcium 800 mg/day
    limitations
    Different population, dose and background supplementation from the 180-microgram trial; the one-year and three-year reports are not independent cohorts.
    nutrient_topic
    Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin K2 / menaquinone family
    organism
    142 postmenopausal women with osteopenia
    plain_language
    Adding K2 changed the protein marker even with calcium and vitamin D already supplied.
    primary_references
    [k2-p33030563] The effect of vitamin MK-7 on bone mineral density and microarchitecture in postmenopausal women with osteopenia, a 3-year randomized, placebo-controlled clinical trial. (2021). https://pubmed.ncbi.nlm.nih.gov/33030563/ DOI: 10.1007/s00198-020-05638-z
    tissue_or_cell_type
    Osteocalcin, DXA and bone microarchitecture

    Vitamin K2: menaquinone forms, carboxylation, recycling and nutrient interactions (2026-09-17) · lines 1085–1096

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Three-year double-blind randomized add-on trial · source_derived_draft · unverified_draft

    ### k2-mk7-cad-carboxylation With calcium and D3 in both groups, MK-7 reduced ucOC by about 65% after one year. Condition category: normal nutrient_topic: Vitamin K2 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Adding K2 changed the protein marker even with calcium and vitamin D already supplied. organism: 142 postmenopausal women with osteopenia tissue_or_cell_type: Osteocalcin, DXA and bone microarchitecture experimental_model: Three-year double-blind randomized add-on trial limitations: Different population, dose and background supplementation from the 180-microgram trial; the one-year and three-year reports are not independent cohorts. exposure: MK-7 375 micrograms/day versus placebo; both groups D3 38 micrograms/day and calcium 800 mg/day evidence_span: {"source_cache": "artifacts/k2-research/33030563.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138", "start_char": 0, "end_char": 2370, "text_sha256": "008ef1b176a3f718d923eea696a7a97b09d64e3079e57c997beaf485153ca138"} [k2-p33030563] The effect of vitamin MK-7 on bone mineral density and microarchitecture in postmenopausal women with osteopenia, a 3-year randomized, placebo-controlled clinical trial. (2021). https://pubmed.ncbi.nlm.nih.gov/33030563/ DOI: 10.1007/s00198-020-05638-z
    Complete structured claim and evidence
  10. Zinc absorption fractions were 32.8±2.3%, 26.9±2.4%, 39.4±2.4% and 26.2±2.3% (mean±SE) for moderate-Ca/low-phytate, moderate-Ca/high-phytate, high-Ca/low-phytate and high-Ca/high-phytate menus. Phytate reduced absorption; calcium did not significantly impair it.

    Phytic acid / phytate → Intestinal zinc absorption source_derived_draftungraded
    Experimental context and source evidence
    absolute_absorption
    Corresponding absolute absorption: 3.8±0.3, 3.0±0.3, 4.5±0.3 and 3.2±0.3 mg zinc/day (mean±SE).
    cross_nutrient
    Calcium (dietary_context); Zinc (measured_nutrient)
    evidence_location
    Indexed primary abstract.
    evidence_span
    {"source_cache": "artifacts/zinc-clinical-sources/hunt2009.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "d912d9f2c0890cde2ae13e9de7f1202bf130e661e3f14e13483563f179319f85", "utf8_bytes": 1659}
    experimental_model
    Two-by-two one-day feeding and 65Zn tracer study in ten healthy women
    exposure
    Approximately 700 versus 1800 mg calcium/day, and 440 versus 1800 mg phytate/day in conventional menus.
    limitations
    Short controlled menus in ten women; null calcium effect does not cover every formulation, population or dose.
    nutrient_topic
    Zinc research collection; topical membership is not evidence of a direct dietary effect. · Zinc
    organism
    Homo sapiens
    plain_language
    Phytate reduced zinc uptake in these menus, while extra calcium did not.
    primary_references
    [zn-clin-hunt2009] Dietary calcium does not exacerbate phytate inhibition of zinc absorption by women from conventional diets. (2009). https://pubmed.ncbi.nlm.nih.gov/19176739/ DOI: 10.3945/ajcn.2008.27175
    tissue_or_cell_type
    Intestinal absorption

    Zinc: transport, enzyme loading, deficiency and nutrient interactions (2026-09-17) · lines 1271–1285

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Two-by-two one-day feeding and 65Zn tracer study in ten healthy women · source_derived_draft · unverified_draft

    ### zn-clin-phytate-calcium Zinc absorption fractions were 32.8±2.3%, 26.9±2.4%, 39.4±2.4% and 26.2±2.3% (mean±SE) for moderate-Ca/low-phytate, moderate-Ca/high-phytate, high-Ca/low-phytate and high-Ca/high-phytate menus. Phytate reduced absorption; calcium did not significantly impair it. Condition category: normal nutrient_topic: Zinc research collection; topical membership is not evidence of a direct dietary effect. plain_language: Phytate reduced zinc uptake in these menus, while extra calcium did not. organism: Homo sapiens tissue_or_cell_type: Intestinal absorption experimental_model: Two-by-two one-day feeding and 65Zn tracer study in ten healthy women limitations: Short controlled menus in ten women; null calcium effect does not cover every formulation, population or dose. exposure: Approximately 700 versus 1800 mg calcium/day, and 440 versus 1800 mg phytate/day in conventional menus. cross_nutrient: Calcium (dietary_context); Zinc (measured_nutrient) evidence_location: Indexed primary abstract. evidence_span: {"source_cache": "artifacts/zinc-clinical-sources/hunt2009.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "d912d9f2c0890cde2ae13e9de7f1202bf130e661e3f14e13483563f179319f85", "utf8_bytes": 1659} absolute_absorption: Corresponding absolute absorption: 3.8±0.3, 3.0±0.3, 4.5±0.3 and 3.2±0.3 mg zinc/day (mean±SE). [zn-clin-hunt2009] Dietary calcium does not exacerbate phytate inhibition of zinc absorption by women from conventional diets. (2009). https://pubmed.ncbi.nlm.nih.gov/19176739/ DOI: 10.3945/ajcn.2008.27175
    Complete structured claim and evidence
  11. At the same ascending phytate-P additions, seven-day calcium retention was 31%, 28%, 27%, 26%, 22%, 19%, 14% and 11%; reduction was significant from 100 mg phytate-P in this study.

    Phytic acid / phytate → Whole-body calcium retention source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Calcium (retained_nutrient); Zinc (concurrently_measured_nutrient)
    evidence_location
    Indexed primary abstract.
    evidence_span
    {"source_cache": "artifacts/zinc-clinical-sources/hallberg2006.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "3a8556f5e4076009ed9adbf018205c8a3b2d0aaae43cccc866dc6be0271451d4", "utf8_bytes": 1603}
    experimental_model
    Human dual-radioisotope meal study: 40 subjects, 105 meals
    exposure
    Wheat-roll meals contained 3.1 mg zinc and 266 mg calcium; added sodium phytate supplied 0–250 mg phytate phosphorus.
    limitations
    Phytate-P mass is phosphorus mass, not total phytate mass. Seven-day calcium retention and zinc absorption are distinct endpoints; meal-specific significance levels are not universal thresholds.
    nutrient_topic
    Zinc research collection; topical membership is not evidence of a direct dietary effect. · Zinc
    organism
    Homo sapiens
    plain_language
    The same meal manipulation also reduced retained calcium.
    primary_references
    [zn-clin-hallberg2006] Absorption of zinc and retention of calcium: dose-dependent inhibition by phytate. (2006). https://pubmed.ncbi.nlm.nih.gov/16632176/ DOI: 10.1016/j.jtemb.2006.01.003
    tissue_or_cell_type
    Intestinal zinc absorption and whole-body calcium retention

    Zinc: transport, enzyme loading, deficiency and nutrient interactions (2026-09-17) · lines 1302–1315

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human dual-radioisotope meal study: 40 subjects, 105 meals · source_derived_draft · unverified_draft

    ### zn-clin-phytate-calcium-retention At the same ascending phytate-P additions, seven-day calcium retention was 31%, 28%, 27%, 26%, 22%, 19%, 14% and 11%; reduction was significant from 100 mg phytate-P in this study. Condition category: normal nutrient_topic: Zinc research collection; topical membership is not evidence of a direct dietary effect. plain_language: The same meal manipulation also reduced retained calcium. organism: Homo sapiens tissue_or_cell_type: Intestinal zinc absorption and whole-body calcium retention experimental_model: Human dual-radioisotope meal study: 40 subjects, 105 meals limitations: Phytate-P mass is phosphorus mass, not total phytate mass. Seven-day calcium retention and zinc absorption are distinct endpoints; meal-specific significance levels are not universal thresholds. exposure: Wheat-roll meals contained 3.1 mg zinc and 266 mg calcium; added sodium phytate supplied 0–250 mg phytate phosphorus. cross_nutrient: Calcium (retained_nutrient); Zinc (concurrently_measured_nutrient) evidence_location: Indexed primary abstract. evidence_span: {"source_cache": "artifacts/zinc-clinical-sources/hallberg2006.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "3a8556f5e4076009ed9adbf018205c8a3b2d0aaae43cccc866dc6be0271451d4", "utf8_bytes": 1603} [zn-clin-hallberg2006] Absorption of zinc and retention of calcium: dose-dependent inhibition by phytate. (2006). https://pubmed.ncbi.nlm.nih.gov/16632176/ DOI: 10.1016/j.jtemb.2006.01.003
    Complete structured claim and evidence
  12. At added phytate-P levels of 0, 25, 50, 75, 100, 140, 175 and 250 mg, mean zinc absorption was 22%, 16%, 14%, 11%, 7%, 7%, 7% and 6%. Reductions were significant from 50 mg phytate-P in these meals.

    Phytic acid / phytate → Intestinal zinc absorption source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Zinc (absorbed_nutrient); Calcium (meal_context)
    evidence_location
    Indexed primary abstract.
    evidence_span
    {"source_cache": "artifacts/zinc-clinical-sources/hallberg2006.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "3a8556f5e4076009ed9adbf018205c8a3b2d0aaae43cccc866dc6be0271451d4", "utf8_bytes": 1603}
    experimental_model
    Human dual-radioisotope meal study: 40 subjects, 105 meals
    exposure
    Wheat-roll meals contained 3.1 mg zinc and 266 mg calcium; added sodium phytate supplied 0–250 mg phytate phosphorus.
    limitations
    Phytate-P mass is phosphorus mass, not total phytate mass. Seven-day calcium retention and zinc absorption are distinct endpoints; meal-specific significance levels are not universal thresholds.
    nutrient_topic
    Zinc research collection; topical membership is not evidence of a direct dietary effect. · Zinc
    organism
    Homo sapiens
    plain_language
    Increasing phytate progressively reduced zinc uptake in the test meal.
    primary_references
    [zn-clin-hallberg2006] Absorption of zinc and retention of calcium: dose-dependent inhibition by phytate. (2006). https://pubmed.ncbi.nlm.nih.gov/16632176/ DOI: 10.1016/j.jtemb.2006.01.003
    tissue_or_cell_type
    Intestinal zinc absorption and whole-body calcium retention

    Zinc: transport, enzyme loading, deficiency and nutrient interactions (2026-09-17) · lines 1287–1300

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Human dual-radioisotope meal study: 40 subjects, 105 meals · source_derived_draft · unverified_draft

    ### zn-clin-phytate-gradient At added phytate-P levels of 0, 25, 50, 75, 100, 140, 175 and 250 mg, mean zinc absorption was 22%, 16%, 14%, 11%, 7%, 7%, 7% and 6%. Reductions were significant from 50 mg phytate-P in these meals. Condition category: normal nutrient_topic: Zinc research collection; topical membership is not evidence of a direct dietary effect. plain_language: Increasing phytate progressively reduced zinc uptake in the test meal. organism: Homo sapiens tissue_or_cell_type: Intestinal zinc absorption and whole-body calcium retention experimental_model: Human dual-radioisotope meal study: 40 subjects, 105 meals limitations: Phytate-P mass is phosphorus mass, not total phytate mass. Seven-day calcium retention and zinc absorption are distinct endpoints; meal-specific significance levels are not universal thresholds. exposure: Wheat-roll meals contained 3.1 mg zinc and 266 mg calcium; added sodium phytate supplied 0–250 mg phytate phosphorus. cross_nutrient: Zinc (absorbed_nutrient); Calcium (meal_context) evidence_location: Indexed primary abstract. evidence_span: {"source_cache": "artifacts/zinc-clinical-sources/hallberg2006.abstract.txt", "locator": "Primary indexed abstract; complete local file", "file_sha256": "3a8556f5e4076009ed9adbf018205c8a3b2d0aaae43cccc866dc6be0271451d4", "utf8_bytes": 1603} [zn-clin-hallberg2006] Absorption of zinc and retention of calcium: dose-dependent inhibition by phytate. (2006). https://pubmed.ncbi.nlm.nih.gov/16632176/ DOI: 10.1016/j.jtemb.2006.01.003
    Complete structured claim and evidence
  13. Increasing boron intake from 0.33 to 3.33 mg/day did not alter the measured mineral absorption or excretion endpoints in the 1993 follow-up study.

    Boron → Urinary calcium excretion source_derived_draftungraded
    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/boron-research/8329361.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3e6e2137f75699ea6dce582375f335a85139fea1cfa7ec502f033e8bfe026d63", "start_char": 0, "end_char": 1079, "text_sha256": "3e6e2137f75699ea6dce582375f335a85139fea1cfa7ec502f033e8bfe026d63"}
    experimental_model
    Metabolic-unit low-intake/supplementation follow-up
    exposure
    0.33 mg boron/day for three weeks, then an additional 3 mg/day for three weeks
    limitations
    Small, short sequential study. The background diet produced positive calcium balance with increased urinary calcium; the authors proposed that this could mask a boron effect, but did not prove the explanation.
    nutrient_topic
    Boron research collection; topical membership is not evidence of a direct dietary effect. · Boron
    organism
    Human postmenopausal volunteers
    plain_language
    This follow-up did not reproduce the earlier calcium-sparing finding.
    primary_references
    [boron-p8329361] The influence of a low-boron diet and boron supplementation on bone, major mineral and sex steroid metabolism in postmenopausal women. (1993). https://pubmed.ncbi.nlm.nih.gov/8329361/ DOI: 10.1079/bjn19930087
    tissue_or_cell_type
    Mineral balance, hormones and bone-turnover markers
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Boron: chemistry, nutrient interactions, low-intake studies and mechanistic uncertainties (2026-09-17) · lines 703–714

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Metabolic-unit low-intake/supplementation follow-up · source_derived_draft · unverified_draft

    ### boron-human-calcium-null-1993 Increasing boron intake from 0.33 to 3.33 mg/day did not alter the measured mineral absorption or excretion endpoints in the 1993 follow-up study. Condition category: nutrient_deficiency nutrient_topic: Boron research collection; topical membership is not evidence of a direct dietary effect. plain_language: This follow-up did not reproduce the earlier calcium-sparing finding. organism: Human postmenopausal volunteers tissue_or_cell_type: Mineral balance, hormones and bone-turnover markers experimental_model: Metabolic-unit low-intake/supplementation follow-up limitations: Small, short sequential study. The background diet produced positive calcium balance with increased urinary calcium; the authors proposed that this could mask a boron effect, but did not prove the explanation. exposure: 0.33 mg boron/day for three weeks, then an additional 3 mg/day for three weeks evidence_span: {"source_cache": "artifacts/boron-research/8329361.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "3e6e2137f75699ea6dce582375f335a85139fea1cfa7ec502f033e8bfe026d63", "start_char": 0, "end_char": 1079, "text_sha256": "3e6e2137f75699ea6dce582375f335a85139fea1cfa7ec502f033e8bfe026d63"} [boron-p8329361] The influence of a low-boron diet and boron supplementation on bone, major mineral and sex steroid metabolism in postmenopausal women. (1993). https://pubmed.ncbi.nlm.nih.gov/8329361/ DOI: 10.1079/bjn19930087
    Complete structured claim and evidence
  14. Changes in testicular calcium, phosphorus and zinc did not precede atrophy in the rat boric-acid study, arguing against those measured changes as the initiating mechanism.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/boron-research/7889890.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "73e5c915a0c7a8fa107ff62480430e94c1cf5c40648f37e08d0266394b05b70a", "start_char": 0, "end_char": 1729, "text_sha256": "73e5c915a0c7a8fa107ff62480430e94c1cf5c40648f37e08d0266394b05b70a"}
    experimental_model
    High-dose rat toxicity experiments with supporting cell assays
    exposure
    High boric-acid exposure; testis boron approximately 1–2 mM
    limitations
    High-exposure animal toxicity does not specify a human dietary threshold. The indexed abstract is truncated; no unreported plasminogen-activator or cAMP result is inferred.
    nutrient_topic
    Boron research collection; topical membership is not evidence of a direct dietary effect. · Boron
    organism
    Rat
    plain_language
    Mineral changes appeared too late to explain the start of the injury in this experiment.
    primary_references
    [boron-p7889890] Mechanism of the testicular toxicity of boric acid in rats: in vivo and in vitro studies. (1994). https://pubmed.ncbi.nlm.nih.gov/7889890/ DOI: 10.1289/ehp.94102s799
    tissue_or_cell_type
    Testis, brain, tissue flavins and isolated Leydig cells

    Boron: chemistry, nutrient interactions, low-intake studies and mechanistic uncertainties (2026-09-17) · lines 1171–1182

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · High-dose rat toxicity experiments with supporting cell assays · source_derived_draft · unverified_draft

    ### boron-rat-testis-minerals-not-upstream Changes in testicular calcium, phosphorus and zinc did not precede atrophy in the rat boric-acid study, arguing against those measured changes as the initiating mechanism. Condition category: normal nutrient_topic: Boron research collection; topical membership is not evidence of a direct dietary effect. plain_language: Mineral changes appeared too late to explain the start of the injury in this experiment. organism: Rat tissue_or_cell_type: Testis, brain, tissue flavins and isolated Leydig cells experimental_model: High-dose rat toxicity experiments with supporting cell assays limitations: High-exposure animal toxicity does not specify a human dietary threshold. The indexed abstract is truncated; no unreported plasminogen-activator or cAMP result is inferred. exposure: High boric-acid exposure; testis boron approximately 1–2 mM evidence_span: {"source_cache": "artifacts/boron-research/7889890.abstract.txt", "locator": "Exact primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "73e5c915a0c7a8fa107ff62480430e94c1cf5c40648f37e08d0266394b05b70a", "start_char": 0, "end_char": 1729, "text_sha256": "73e5c915a0c7a8fa107ff62480430e94c1cf5c40648f37e08d0266394b05b70a"} [boron-p7889890] Mechanism of the testicular toxicity of boric acid in rats: in vivo and in vitro studies. (1994). https://pubmed.ncbi.nlm.nih.gov/7889890/ DOI: 10.1289/ehp.94102s799
    Complete structured claim and evidence
  15. Oral calcium supplementation reversed the metformin-induced depression of serum holotranscobalamin.

    Experimental context and source evidence
    availability_state
    nutrient_deficiency Imported condition classification; unverified.
    evidence_span
    {"source_cache": "artifacts/metformin-research/10977010.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7aed1bfb7ee680b248e083db467fd4a8199ac933e8a12b4c6ba08f9931a7794b", "start_char": 0, "end_char": 1267, "text_sha256": "7aed1bfb7ee680b248e083db467fd4a8199ac933e8a12b4c6ba08f9931a7794b"}
    experimental_model
    Comparative study in 21 people with type 2 diabetes, 14 switched to metformin, with oral calcium supplementation
    exposure
    Metformin for three months, then oral calcium supplementation
    limitations
    A small, non-randomised comparative study. The calcium-dependent ileal mechanism is the authors’ interpretation of the reversal, not a direct measurement of receptor binding.
    nutrient_topic
    Metformin research collection; topical membership is not evidence of a direct clinical effect, and pharmacological exposure is not dietary intake. · Metformin
    organism
    Human
    plain_language
    Adding calcium undid the drug’s effect on the vitamin.
    primary_references
    [metformin-p10977010] Increased intake of calcium reverses vitamin B12 malabsorption induced by metformin. (2000). https://pubmed.ncbi.nlm.nih.gov/10977010/ DOI: 10.2337/diacare.23.9.1227
    tissue_or_cell_type
    Ileal absorption
    trigger_kind
    nutrient_deficiency Imported condition classification; unverified.

    Metformin: transport, molecular targets, gut mechanisms and nutrient interactions (2026-09-19) · lines 1139–1150

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Comparative study in 21 people with type 2 diabetes, 14 switched to metformin, with oral calcium supplementation · source_derived_draft · unverified_draft

    ### metformin-b12-calcium-reversal Oral calcium supplementation reversed the metformin-induced depression of serum holotranscobalamin. Condition category: nutrient_deficiency nutrient_topic: Metformin research collection; topical membership is not evidence of a direct clinical effect, and pharmacological exposure is not dietary intake. plain_language: Adding calcium undid the drug’s effect on the vitamin. organism: Human tissue_or_cell_type: Ileal absorption experimental_model: Comparative study in 21 people with type 2 diabetes, 14 switched to metformin, with oral calcium supplementation limitations: A small, non-randomised comparative study. The calcium-dependent ileal mechanism is the authors’ interpretation of the reversal, not a direct measurement of receptor binding. exposure: Metformin for three months, then oral calcium supplementation evidence_span: {"source_cache": "artifacts/metformin-research/10977010.abstract.txt", "locator": "Indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "7aed1bfb7ee680b248e083db467fd4a8199ac933e8a12b4c6ba08f9931a7794b", "start_char": 0, "end_char": 1267, "text_sha256": "7aed1bfb7ee680b248e083db467fd4a8199ac933e8a12b4c6ba08f9931a7794b"} [metformin-p10977010] Increased intake of calcium reverses vitamin B12 malabsorption induced by metformin. (2000). https://pubmed.ncbi.nlm.nih.gov/10977010/ DOI: 10.2337/diacare.23.9.1227
    Complete structured claim and evidence
  16. After normalization to milk protein, calcium and manganese were lower in milk from Tmem165-deficient dams.

    Experimental context and source evidence
    availability_state
    machinery_impairment Imported condition classification; unverified.
    cross_nutrient
    Mouse TMEM165 (affected_protein); Milk calcium normalized to protein (measured_endpoint); Calcium (affected_nutrient); Manganese (affected_nutrient)
    evidence_span
    {"source_cache": "artifacts/manganese-glycosylation-sources/milk2019.abstract.txt", "locator": "Indexed primary abstract", "file_sha256": "88bcb50ecdb918803c5950bcff8f48665dbd17148b365a4f9f3b463fe7edd2a4", "start_char": 0, "end_char": 1462, "text_sha256": "88bcb50ecdb918803c5950bcff8f48665dbd17148b365a4f9f3b463fe7edd2a4", "text_characters": 1462}
    experimental_model
    Conditional mammary epithelial Tmem165 deletion in mice
    exposure
    Tissue-specific deletion with milk composition and pup-growth measurements.
    limitations
    The primary abstract supports normalized milk minerals and reduced lactose; altered concentration can reflect less milk dilution. Proposed cation/H+ exchange is an interpretation, not a transport stoichiometry measured here.
    nutrient_topic
    Manganese research collection; topical membership is not evidence of a direct dietary effect. · Manganese
    organism
    Mus musculus
    plain_language
    The defect changed milk manganese and calcium relative to its protein content.
    primary_references
    [mn-gly-milk2019] Milk biosynthesis requires the Golgi cation exchanger TMEM165. (2019). https://pubmed.ncbi.nlm.nih.gov/30622138/ DOI: 10.1074/jbc.ra118.006270
    tissue_or_cell_type
    Lactating mammary gland and milk
    trigger_kind
    machinery_impairment Imported condition classification; unverified.

    Manganese: enzyme cofactors, glycosylation, transport and nutrient interactions (2026-09-17) · lines 894–906

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Conditional mammary epithelial Tmem165 deletion in mice · source_derived_draft · unverified_draft

    ### mn-gly-mammary-minerals After normalization to milk protein, calcium and manganese were lower in milk from Tmem165-deficient dams. Condition category: machinery_impairment nutrient_topic: Manganese research collection; topical membership is not evidence of a direct dietary effect. plain_language: The defect changed milk manganese and calcium relative to its protein content. organism: Mus musculus tissue_or_cell_type: Lactating mammary gland and milk experimental_model: Conditional mammary epithelial Tmem165 deletion in mice limitations: The primary abstract supports normalized milk minerals and reduced lactose; altered concentration can reflect less milk dilution. Proposed cation/H+ exchange is an interpretation, not a transport stoichiometry measured here. exposure: Tissue-specific deletion with milk composition and pup-growth measurements. cross_nutrient: Mouse TMEM165 (affected_protein); Milk calcium normalized to protein (measured_endpoint); Calcium (affected_nutrient); Manganese (affected_nutrient) evidence_span: {"source_cache": "artifacts/manganese-glycosylation-sources/milk2019.abstract.txt", "locator": "Indexed primary abstract", "file_sha256": "88bcb50ecdb918803c5950bcff8f48665dbd17148b365a4f9f3b463fe7edd2a4", "start_char": 0, "end_char": 1462, "text_sha256": "88bcb50ecdb918803c5950bcff8f48665dbd17148b365a4f9f3b463fe7edd2a4", "text_characters": 1462} [mn-gly-milk2019] Milk biosynthesis requires the Golgi cation exchanger TMEM165. (2019). https://pubmed.ncbi.nlm.nih.gov/30622138/ DOI: 10.1074/jbc.ra118.006270
    Complete structured claim and evidence
  17. The responder subset had a Tiselius Risk Index of 1.10 with versus 0.76 without supplementation.

    L-Ascorbic acid → Tiselius calcium oxalate risk index source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    Calcium/oxalate urinary chemistry connects a vitamin metabolite to mineral precipitation risk.
    experimental_model
    Randomized controlled-diet crossover study: 29 calcium stone formers and 19 non-stone formers.
    exposure
    Ascorbic acid 1000 mg twice daily for six days versus no supplement for six days; 13C2 oxalate challenge after adaptation.
    limitations
    Calculated risk is not observed stone formation; this is distinct from a directly measured calcium oxalate activity product.
    nutrient_topic
    Vitamin C research collection; topical membership is not evidence of a direct dietary effect. · Vitamin C
    organism
    Homo sapiens
    plain_language
    Their urine measurements shifted toward a higher calculated calcium oxalate stone risk.
    primary_references
    [c-massey2005] Ascorbate increases human oxaluria and kidney stone risk (2005). https://pubmed.ncbi.nlm.nih.gov/15987848/ DOI: 10.1093/jn/135.7.1673
    tissue_or_cell_type
    Human blood or whole-person endpoints

    Vitamin C: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1682–1693

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized controlled-diet crossover study: 29 calcium stone formers and 19 non-stone formers. · source_derived_draft · unverified_draft

    ### c-high-oral-dose-calcium-oxalate-index The responder subset had a Tiselius Risk Index of 1.10 with versus 0.76 without supplementation. Condition category: normal nutrient_topic: Vitamin C research collection; topical membership is not evidence of a direct dietary effect. plain_language: Their urine measurements shifted toward a higher calculated calcium oxalate stone risk. organism: Homo sapiens tissue_or_cell_type: Human blood or whole-person endpoints experimental_model: Randomized controlled-diet crossover study: 29 calcium stone formers and 19 non-stone formers. limitations: Calculated risk is not observed stone formation; this is distinct from a directly measured calcium oxalate activity product. exposure: Ascorbic acid 1000 mg twice daily for six days versus no supplement for six days; 13C2 oxalate challenge after adaptation. cross_nutrient: Calcium/oxalate urinary chemistry connects a vitamin metabolite to mineral precipitation risk. [c-massey2005] Ascorbate increases human oxaluria and kidney stone risk (2005). https://pubmed.ncbi.nlm.nih.gov/15987848/ DOI: 10.1093/jn/135.7.1673
    Complete structured claim and evidence
  18. Calcium balance was unchanged during the tested pectin feeding period.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/pectin-research/37887.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ad5427835e84a210b32e8ceea45baeece0bc1e4488d5852a5b4244f51dc32a69", "start_char": 0, "end_char": 1141, "text_sha256": "ad5427835e84a210b32e8ceea45baeece0bc1e4488d5852a5b4244f51dc32a69"}
    experimental_model
    Controlled feeding and balance study in five healthy men
    exposure
    Nine-week protocol; 36 g/day pectin during last six weeks
    limitations
    Small older study. Disappearance from stool supported fermentation but did not assign a particular enzyme or metabolic flux.
    nutrient_topic
    Pectin research collection; topical membership is not evidence of a direct dietary effect. · Pectin, structurally heterogeneous plant polysaccharides
    organism
    Homo sapiens
    plain_language
    Mineral binding in a test tube did not imply a calcium deficit here.
    primary_references
    [pectin-p37887] The digestion of pectin in the human gut and its effect on calcium absorption and large bowel function. (1979). https://pubmed.ncbi.nlm.nih.gov/37887/ DOI: 10.1079/bjn19790062
    tissue_or_cell_type
    Whole-gut balance and stool

    Pectin: metabolism, signaling and nutrient connections (2026-09-17) · lines 750–761

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Controlled feeding and balance study in five healthy men · source_derived_draft · unverified_draft

    ### pectin-calcium-balance-null Calcium balance was unchanged during the tested pectin feeding period. Condition category: normal nutrient_topic: Pectin research collection; topical membership is not evidence of a direct dietary effect. plain_language: Mineral binding in a test tube did not imply a calcium deficit here. organism: Homo sapiens tissue_or_cell_type: Whole-gut balance and stool experimental_model: Controlled feeding and balance study in five healthy men limitations: Small older study. Disappearance from stool supported fermentation but did not assign a particular enzyme or metabolic flux. exposure: Nine-week protocol; 36 g/day pectin during last six weeks evidence_span: {"source_cache": "artifacts/pectin-research/37887.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ad5427835e84a210b32e8ceea45baeece0bc1e4488d5852a5b4244f51dc32a69", "start_char": 0, "end_char": 1141, "text_sha256": "ad5427835e84a210b32e8ceea45baeece0bc1e4488d5852a5b4244f51dc32a69"} [pectin-p37887] The digestion of pectin in the human gut and its effect on calcium absorption and large bowel function. (1979). https://pubmed.ncbi.nlm.nih.gov/37887/ DOI: 10.1079/bjn19790062
    Complete structured claim and evidence
  19. Apparent calcium absorption was unchanged in the ileostomy study.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/pectin-research/6307932.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1", "start_char": 0, "end_char": 1593, "text_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1"}
    experimental_model
    Within-person ileostomy balance study; six participants
    exposure
    15 g/day citrus pectin on days 5-7 of a 10-day low-fiber feeding protocol
    limitations
    Ileal apparent absorption and output are not whole-body status or clinical deficiency; the colon was bypassed.
    nutrient_topic
    Pectin research collection; topical membership is not evidence of a direct dietary effect. · Pectin, structurally heterogeneous plant polysaccharides
    organism
    Homo sapiens
    plain_language
    The effect on iron did not extend to every mineral.
    primary_references
    [pectin-p6307932] The effect of citrus pectin on the absorption of nutrients in the small intestine. (1983). https://pubmed.ncbi.nlm.nih.gov/6307932/
    tissue_or_cell_type
    Small intestine; ileal effluent

    Pectin: metabolism, signaling and nutrient connections (2026-09-17) · lines 607–618

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Within-person ileostomy balance study; six participants · source_derived_draft · unverified_draft

    ### pectin-ileal-calcium-null Apparent calcium absorption was unchanged in the ileostomy study. Condition category: normal nutrient_topic: Pectin research collection; topical membership is not evidence of a direct dietary effect. plain_language: The effect on iron did not extend to every mineral. organism: Homo sapiens tissue_or_cell_type: Small intestine; ileal effluent experimental_model: Within-person ileostomy balance study; six participants limitations: Ileal apparent absorption and output are not whole-body status or clinical deficiency; the colon was bypassed. exposure: 15 g/day citrus pectin on days 5-7 of a 10-day low-fiber feeding protocol evidence_span: {"source_cache": "artifacts/pectin-research/6307932.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1", "start_char": 0, "end_char": 1593, "text_sha256": "fd45607a7ff1d1a20dd52d145134da591847919c3db47ef8a8cf5693fb9f80a1"} [pectin-p6307932] The effect of citrus pectin on the absorption of nutrients in the small intestine. (1983). https://pubmed.ncbi.nlm.nih.gov/6307932/
    Complete structured claim and evidence
  20. Intact FGF23 rose from 33 to 37 ng/L during the higher-phosphate/calcium regimen.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"}
    experimental_model
    Paired 36-hour dietary interventions
    exposure
    Low/high phosphate and calcium diets, separated by a week
    limitations
    Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter.
    nutrient_topic
    Phosphorus research collection; topical membership is not evidence of a direct dietary effect. · Phosphorus
    organism
    Human
    plain_language
    The active hormone concentration also increased.
    primary_references
    [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    tissue_or_cell_type
    Ten healthy adults; serial serum measurements and 24-hour urine

    Phosphorus: metabolism, signaling and nutrient connections (2026-09-17) · lines 946–957

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Paired 36-hour dietary interventions · source_derived_draft · unverified_draft

    ### phosphorus-mixed-diet-fgf23 Intact FGF23 rose from 33 to 37 ng/L during the higher-phosphate/calcium regimen. Condition category: normal nutrient_topic: Phosphorus research collection; topical membership is not evidence of a direct dietary effect. plain_language: The active hormone concentration also increased. organism: Human tissue_or_cell_type: Ten healthy adults; serial serum measurements and 24-hour urine experimental_model: Paired 36-hour dietary interventions limitations: Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter. exposure: Low/high phosphate and calcium diets, separated by a week evidence_span: {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"} [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    Complete structured claim and evidence
  21. Serum phosphate rose from 1.11 to 1.32 mmol/L during the higher-phosphate/calcium regimen.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"}
    experimental_model
    Paired 36-hour dietary interventions
    exposure
    Low/high phosphate and calcium diets, separated by a week
    limitations
    Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter.
    nutrient_topic
    Phosphorus research collection; topical membership is not evidence of a direct dietary effect. · Phosphorus
    organism
    Human
    plain_language
    The combined dietary change raised the blood phosphate measurement.
    primary_references
    [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    tissue_or_cell_type
    Ten healthy adults; serial serum measurements and 24-hour urine

    Phosphorus: metabolism, signaling and nutrient connections (2026-09-17) · lines 933–944

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Paired 36-hour dietary interventions · source_derived_draft · unverified_draft

    ### phosphorus-mixed-diet-pi Serum phosphate rose from 1.11 to 1.32 mmol/L during the higher-phosphate/calcium regimen. Condition category: normal nutrient_topic: Phosphorus research collection; topical membership is not evidence of a direct dietary effect. plain_language: The combined dietary change raised the blood phosphate measurement. organism: Human tissue_or_cell_type: Ten healthy adults; serial serum measurements and 24-hour urine experimental_model: Paired 36-hour dietary interventions limitations: Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter. exposure: Low/high phosphate and calcium diets, separated by a week evidence_span: {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"} [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    Complete structured claim and evidence
  22. PTH declined during the higher-phosphate/calcium regimen even while FGF23 increased.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"}
    experimental_model
    Paired 36-hour dietary interventions
    exposure
    Low/high phosphate and calcium diets, separated by a week
    limitations
    Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter.
    nutrient_topic
    Phosphorus research collection; topical membership is not evidence of a direct dietary effect. · Phosphorus
    organism
    Human
    plain_language
    Changing calcium alongside phosphate produced a different PTH pattern than a phosphate-only cell challenge.
    primary_references
    [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    tissue_or_cell_type
    Ten healthy adults; serial serum measurements and 24-hour urine

    Phosphorus: metabolism, signaling and nutrient connections (2026-09-17) · lines 972–983

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Paired 36-hour dietary interventions · source_derived_draft · unverified_draft

    ### phosphorus-mixed-diet-pth PTH declined during the higher-phosphate/calcium regimen even while FGF23 increased. Condition category: normal nutrient_topic: Phosphorus research collection; topical membership is not evidence of a direct dietary effect. plain_language: Changing calcium alongside phosphate produced a different PTH pattern than a phosphate-only cell challenge. organism: Human tissue_or_cell_type: Ten healthy adults; serial serum measurements and 24-hour urine experimental_model: Paired 36-hour dietary interventions limitations: Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter. exposure: Low/high phosphate and calcium diets, separated by a week evidence_span: {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"} [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    Complete structured claim and evidence
  23. Urinary phosphate rose from 21.6 to 28.8 mmol/day during the higher-phosphate/calcium regimen.

    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"}
    experimental_model
    Paired 36-hour dietary interventions
    exposure
    Low/high phosphate and calcium diets, separated by a week
    limitations
    Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter.
    nutrient_topic
    Phosphorus research collection; topical membership is not evidence of a direct dietary effect. · Phosphorus
    organism
    Human
    plain_language
    The kidneys excreted more phosphate.
    primary_references
    [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    tissue_or_cell_type
    Ten healthy adults; serial serum measurements and 24-hour urine

    Phosphorus: metabolism, signaling and nutrient connections (2026-09-17) · lines 959–970

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Paired 36-hour dietary interventions · source_derived_draft · unverified_draft

    ### phosphorus-mixed-diet-urine Urinary phosphate rose from 21.6 to 28.8 mmol/day during the higher-phosphate/calcium regimen. Condition category: normal nutrient_topic: Phosphorus research collection; topical membership is not evidence of a direct dietary effect. plain_language: The kidneys excreted more phosphate. organism: Human tissue_or_cell_type: Ten healthy adults; serial serum measurements and 24-hour urine experimental_model: Paired 36-hour dietary interventions limitations: Both calcium and phosphate changed; phosphate alone cannot be assigned the full effect. Timing and circadian variation matter. exposure: Low/high phosphate and calcium diets, separated by a week evidence_span: {"source_cache": "artifacts/phosphorus-research/21030580.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e", "start_char": 0, "end_char": 1603, "text_sha256": "e51a1cd580ac4ea7b0232f65c73ac0814df6bff655bf7bd6d0d82f7f9f21a33e"} [phosphorus-p21030580] Effects of dietary phosphate and calcium intake on fibroblast growth factor-23. (2011). https://pubmed.ncbi.nlm.nih.gov/21030580/ DOI: 10.2215/cjn.04730510
    Complete structured claim and evidence

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