Component
HOMA-IR in the histidine metabolic-syndrome trial
Context-specific entity; species, compartment and exposure are stated on each claim.
1 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.
Other things that act on it
Enzymes, hormones, genes, and other components with a recorded effect. These are not nutrients, so they do not count toward the arrows above. Each finding names the chapter that recorded it.
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.
What acts on it
In a randomized blinded trial of 100 obese women with metabolic syndrome, 4 g/day histidine for 12 weeks reduced HOMA-IR relative to placebo among 92 completers.
Experimental context and source evidence
- evidence_access
- Primary abstract
- experimental_model
- Women aged 33-51; 50 assigned per arm, 45 histidine and 47 placebo completed.
- limitations
- HOMA-IR is a surrogate; one population and duration. Separate adipocyte experiments do not prove the human mechanism; not a contradiction of isolated microbial-metabolite administration.
- nutrient_topic
- L-Histidine collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · L-Histidine
- plain_language
- A human trial measured improved insulin-resistance-related outcomes in a selected group.
- primary_references
- Histidine supplementation improves insulin resistance through suppressed inflammation in obese women with the metabolic syndrome: a randomised controlled trial. · 2013 · https://pubmed.ncbi.nlm.nih.gov/23361591/ · DOI 10.1007/s00125-013-2839-7
L-Histidine: supply, catabolism, histamine, receptors and cross-nutrient mechanisms (2026-09-19) · lines 450–456
AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · Women aged 33-51; 50 assigned per arm, 45 histidine and 47 placebo completed. · source_derived_draft · unverified_draft
## histidine-metabolic-human-trial A human trial measured improved insulin-resistance-related outcomes in a selected group. In a randomized blinded trial of 100 obese women with metabolic syndrome, 4 g/day histidine for 12 weeks reduced HOMA-IR relative to placebo among 92 completers. Model: Women aged 33-51; 50 assigned per arm, 45 histidine and 47 placebo completed. Limitations: HOMA-IR is a surrogate; one population and duration. Separate adipocyte experiments do not prove the human mechanism; not a contradiction of isolated microbial-metabolite administration. Evidence access: Primary abstract Histidine supplementation improves insulin resistance through suppressed inflammation in obese women with the metabolic syndrome: a randomised controlled trial. · 2013 · https://pubmed.ncbi.nlm.nih.gov/23361591/ · DOI 10.1007/s00125-013-2839-7
Complete structured claim and evidence
The events it takes part in
A mechanism often involves more than two components. These are the full events, with every participant and its role.
Situations it appears in
Low-supply and faulty-machinery situations recorded in the chapters where this component plays a part.
In the sources
Preserved passages that mention this component, quoted exactly. Open one to read it in context.
Open hypotheses
Proposed ideas that involve this component. They are labeled as hypotheses and do not change any recorded statement.
This is a research prototype built from draft material. It is not medical advice, and its statements still await verification against the original studies.