Component

Plasma clozapine exposure

Plasma clozapine exposure. Species, exposure and limitations are retained in each linked claim.

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. Caffeine-derived CYP1A2 indices correlated with clozapine clearance in the 14-person study.

    CYP1A2 catalytic activity → Plasma clozapine exposure source_derived_draftungraded
    Experimental context and source evidence
    evidence_span
    {"source_cache": "artifacts/dim-research/7893591.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d568c4f2cdf1fc2d58f2ea22e395a7d7813cef2b1433fe25da51a2c40df5c545", "start_char": 0, "end_char": 849, "text_sha256": "d568c4f2cdf1fc2d58f2ea22e395a7d7813cef2b1433fe25da51a2c40df5c545"}
    experimental_model
    Clinical caffeine phenotyping and prior clozapine exposure
    exposure
    Caffeine test related to single-dose clozapine kinetics
    limitations
    Correlation supports enzyme relevance; no DIM administration or prediction of an individual clinical effect.
    nutrient_topic
    Diindolylmethane (DIM) research collection; topical membership is not evidence of a direct dietary effect. · 3,3'-Diindolylmethane / DIM
    organism
    14 healthy adults
    plain_language
    Enzyme activity was linked to drug handling in people, separately from any DIM exposure.
    primary_references
    [dim-p7893591] Clozapine disposition covaries with CYP1A2 activity determined by a caffeine test. (1994). https://pubmed.ncbi.nlm.nih.gov/7893591/ DOI: 10.1111/j.1365-2125.1994.tb04385.x
    tissue_or_cell_type
    CYP1A2 phenotype and clozapine disposition

    Diindolylmethane (DIM): formation, receptor signaling, metabolism and drug interactions (2026-09-17) · lines 688–699

    AI-assisted literature curation; primary study URLs and scope retained in the document and extraction. Not publisher full text. · supports · Clinical caffeine phenotyping and prior clozapine exposure · source_derived_draft · unverified_draft

    ### dim-clozapine-phenotype Caffeine-derived CYP1A2 indices correlated with clozapine clearance in the 14-person study. Condition category: normal nutrient_topic: Diindolylmethane (DIM) research collection; topical membership is not evidence of a direct dietary effect. plain_language: Enzyme activity was linked to drug handling in people, separately from any DIM exposure. organism: 14 healthy adults tissue_or_cell_type: CYP1A2 phenotype and clozapine disposition experimental_model: Clinical caffeine phenotyping and prior clozapine exposure limitations: Correlation supports enzyme relevance; no DIM administration or prediction of an individual clinical effect. exposure: Caffeine test related to single-dose clozapine kinetics evidence_span: {"source_cache": "artifacts/dim-research/7893591.abstract.txt", "locator": "Primary indexed abstract; zero-based, end-exclusive Unicode character offsets", "file_sha256": "d568c4f2cdf1fc2d58f2ea22e395a7d7813cef2b1433fe25da51a2c40df5c545", "start_char": 0, "end_char": 849, "text_sha256": "d568c4f2cdf1fc2d58f2ea22e395a7d7813cef2b1433fe25da51a2c40df5c545"} [dim-p7893591] Clozapine disposition covaries with CYP1A2 activity determined by a caffeine test. (1994). https://pubmed.ncbi.nlm.nih.gov/7893591/ DOI: 10.1111/j.1365-2125.1994.tb04385.x
    Complete structured claim and evidence
  2. Caffeine coadministration increased mean clozapine AUC by 19% in the crossover experiment.

    Caffeine → Plasma clozapine exposure source_derived_draftungraded
    Experimental context and source evidence
    evidence_access
    Primary abstract
    experimental_model
    12 nonsmoking healthy men; single 12.5 mg clozapine; caffeine 400–1000 mg/day, mean 550.
    limitations
    Small healthy-volunteer study; patient effect size and toxicity cannot be inferred for an individual.
    nutrient_topic
    Caffeine collection; salts, coffee, species and coexposure contexts retain their identities. · Caffeine
    plain_language
    Caffeine changed exposure to a drug sharing its metabolic pathway.
    primary_references
    Effect of caffeine on clozapine pharmacokinetics in healthy volunteers. · 2000 · https://pubmed.ncbi.nlm.nih.gov/10606838/ · DOI 10.1046/j.1365-2125.2000.00111.x

    Caffeine: receptors, metabolism, nutrient interactions, adaptation and discovery questions (2026-09-18) · lines 268–274

    AI-assisted research curation; primary-abstract references and experimental limitations individually identified. Not publisher full text. · supports · 12 nonsmoking healthy men; single 12.5 mg clozapine; caffeine 400–1000 mg/day, mean 550. · source_derived_draft · unverified_draft

    ## caf-clozapine-auc Caffeine changed exposure to a drug sharing its metabolic pathway. Caffeine coadministration increased mean clozapine AUC by 19% in the crossover experiment. Model: 12 nonsmoking healthy men; single 12.5 mg clozapine; caffeine 400–1000 mg/day, mean 550. Limitations: Small healthy-volunteer study; patient effect size and toxicity cannot be inferred for an individual. Evidence access: Primary abstract Effect of caffeine on clozapine pharmacokinetics in healthy volunteers. · 2000 · https://pubmed.ncbi.nlm.nih.gov/10606838/ · DOI 10.1046/j.1365-2125.2000.00111.x
    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