Component

Total fracture incidence

Study-defined Total fracture incidence. Read each linked record for species, exposure and endpoint.

2 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 acts on it

  1. There were 171 versus 135 fractures; fracture rate ratio 1.26 (95% CI1.00–1.59; P=0.047) for annual D3 versus placebo.

    Cholecalciferol → Total fracture incidence source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    false
    experimental_model
    2256 community-dwelling women aged≥ 70; annual-bolus randomized placebo-controlled trial
    exposure
    500, 000 IU oral D3 each autumn/winter for 3–5 years.
    limitations
    Annual very large bolus in older women; does not demonstrate that all D3 regimens raise risk.
    nutrient_topic
    Vitamin D2 and D3 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin D2 and D3
    organism
    Homo sapiens
    plain_language
    Fractures were also more frequent under that specific regimen.
    primary_references
    [sanders2010] Annual high-dose oral vitamin D and falls and fractures in older women: a randomized controlled trial. (2010). https://pubmed.ncbi.nlm.nih.gov/20460620/ DOI: 10.1001/jama.2010.594
    tissue_or_cell_type
    Clinical skeletal outcomes

    Vitamin D2 and D3: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1587–1598

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · 2256 community-dwelling women aged≥ 70; annual-bolus randomized placebo-controlled trial · source_derived_draft · unverified_draft

    ### vd-sanders-fractures There were 171 versus 135 fractures; fracture rate ratio 1.26 (95% CI1.00–1.59; P=0.047) for annual D3 versus placebo. Condition category: normal nutrient_topic: Vitamin D2 and D3 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Fractures were also more frequent under that specific regimen. organism: Homo sapiens tissue_or_cell_type: Clinical skeletal outcomes experimental_model: 2256 community-dwelling women aged≥ 70; annual-bolus randomized placebo-controlled trial limitations: Annual very large bolus in older women; does not demonstrate that all D3 regimens raise risk. exposure: 500, 000 IU oral D3 each autumn/winter for 3–5 years. cross_nutrient: false [sanders2010] Annual high-dose oral vitamin D and falls and fractures in older women: a randomized controlled trial. (2010). https://pubmed.ncbi.nlm.nih.gov/20460620/ DOI: 10.1001/jama.2010.594
    Complete structured claim and evidence
  2. D3 assignment did not significantly reduce total fractures (HR0.98; 95% CI0.89–1.08; P=0.70).

    Cholecalciferol → Total fracture incidence source_derived_draftungraded
    Experimental context and source evidence
    cross_nutrient
    false
    experimental_model
    VITAL ancillary fracture trial; 25, 871 adults; median 5.3 years
    exposure
    D3 2000 IU/day versus placebo; randomized factorial omega 3 allocation; median 5.3 years.
    limitations
    Generally healthy midlife/older adults not selected for deficiency. Does not test treatment of established deficiency rickets or osteomalacia.
    nutrient_topic
    Vitamin D2 and D3 research collection; topical membership is not evidence of a direct dietary effect. · Vitamin D2 and D3
    organism
    Homo sapiens
    plain_language
    Extra D3 did not reduce this fracture endpoint in the population studied.
    primary_references
    [leboff2022] Supplemental Vitamin D and Incident Fractures in Midlife and Older Adults. (2022). https://pubmed.ncbi.nlm.nih.gov/35939577/ DOI: 10.1056/nejmoa2202106
    tissue_or_cell_type
    Clinical skeletal outcomes

    Vitamin D2 and D3: mechanisms, deficiency and nutrient interactions (2026-09-17) · lines 1496–1507

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · VITAL ancillary fracture trial; 25, 871 adults; median 5.3 years · source_derived_draft · unverified_draft

    ### vd-vital-fracture-total D3 assignment did not significantly reduce total fractures (HR0.98; 95% CI0.89–1.08; P=0.70). Condition category: normal nutrient_topic: Vitamin D2 and D3 research collection; topical membership is not evidence of a direct dietary effect. plain_language: Extra D3 did not reduce this fracture endpoint in the population studied. organism: Homo sapiens tissue_or_cell_type: Clinical skeletal outcomes experimental_model: VITAL ancillary fracture trial; 25, 871 adults; median 5.3 years limitations: Generally healthy midlife/older adults not selected for deficiency. Does not test treatment of established deficiency rickets or osteomalacia. exposure: D3 2000 IU/day versus placebo; randomized factorial omega 3 allocation; median 5.3 years. cross_nutrient: false [leboff2022] Supplemental Vitamin D and Incident Fractures in Midlife and Older Adults. (2022). https://pubmed.ncbi.nlm.nih.gov/35939577/ DOI: 10.1056/nejmoa2202106
    Complete structured claim and evidence

In the sources

Preserved passages that mention this component, quoted exactly. Open one to read it in context.

    This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.

    Evidence, AI assistance and curation standards