Component

Skin-prick response in the CHD-FA atopy 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.

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. The small oral CHD-FA trial reported reduced skin-prick responses.

    Experimental context and source evidence
    evidence_access
    Primary abstract
    experimental_model
    30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week.
    limitations
    Short duration and a surrogate endpoint do not establish treatment of allergic disease or effects of other preparations.
    nutrient_topic
    Fulvic acid collection; species, compartment, exposure, co-substrates and manipulation remain explicit. · Fulvic acid (heterogeneous humic fraction)
    plain_language
    An allergy-test response changed in a short trial.
    primary_references
    Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784

    Fulvic acid: mixture identity, mineral chemistry, signaling and cross-nutrient mechanisms (2026-09-19) · lines 260–266

    AI-assisted research curation; primary references, access levels and experimental limitations individually identified. Not publisher full text. · supports · 30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week. · source_derived_draft · unverified_draft

    ## fulvic-acid-human-atopy An allergy-test response changed in a short trial. The small oral CHD-FA trial reported reduced skin-prick responses. Model: 30 atopic men; escalating exposure and crossover component, 3.8% solution up to 40 mL twice daily for one week. Limitations: Short duration and a surrogate endpoint do not establish treatment of allergic disease or effects of other preparations. Evidence access: Primary abstract Phase 1 clinical study of the acute and subacute safety and proof-of-concept efficacy of carbohydrate-derived fulvic acid. · 2012 · https://pubmed.ncbi.nlm.nih.gov/22427734/ · DOI 10.2147/CPAA.S25784
    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