Component

HDL3-associated LCAT activity

HDL3-associated LCAT activity. Species, exposure and limitations are retained in each linked 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 lycopene-supplement arm increased HDL3-associated LCAT activity.

    Lycopene → HDL3-associated LCAT activity source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"}
    experimental_model
    Randomized diet/supplement trial biomarker analysis
    exposure
    Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement
    limitations
    Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events.
    nutrient_topic
    Lycopene research collection; topical membership is not evidence of a direct dietary effect. · Lycopene
    organism
    Human, 225 adults aged 40-65 years
    plain_language
    A cholesterol-handling enzyme changed in this fraction.
    primary_references
    [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
    tissue_or_cell_type
    HDL fractions and plasma lipoproteins

    Lycopene: absorption, metabolism, nutrient connections and human outcomes (2026-09-17) · lines 1027–1038

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Randomized diet/supplement trial biomarker analysis · source_derived_draft · unverified_draft

    ### lycopene-hdl-lcat The lycopene-supplement arm increased HDL3-associated LCAT activity. Condition category: normal nutrient_topic: Lycopene research collection; topical membership is not evidence of a direct dietary effect. plain_language: A cholesterol-handling enzyme changed in this fraction. organism: Human, 225 adults aged 40-65 years tissue_or_cell_type: HDL fractions and plasma lipoproteins experimental_model: Randomized diet/supplement trial biomarker analysis limitations: Food and supplement doses differ; enzyme activities and particle sizes are surrogate endpoints, not proof of fewer events. exposure: Low tomato control; 224-350 mg/week food lycopene; or 70 mg/week supplement evidence_span: {"source_cache": "artifacts/lycopene-research/35978954.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a", "start_char": 0, "end_char": 2778, "text_sha256": "ed024b652760ea2f5ab124162690901b3e88995ea9648bea05b59f240de08c3a"} [lycopene-p35978954] Lycopene-rich diets modulate HDL functionality and associated inflammatory markers without affecting lipoprotein size and distribution in moderately overweight, disease-free, middle-aged adults: A randomized controlled trial. (2022). https://pubmed.ncbi.nlm.nih.gov/35978954/ DOI: 10.3389/fnut.2022.954593
    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