Component

Activated partial thromboplastin time

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. Activated partial thromboplastin time was prolonged significantly at 2 and 4 h after the same single dose.

    Experimental context and source evidence
    duration
    Single dose, sampling to 8 h
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    experimental_model
    Human (12 healthy young males)
    exposure
    NSK-SD, 2,000 FU single dose
    limitations
    Within the normal range. This is one of the two findings that make an additive effect with an antithrombotic drug biologically plausible.
    organism
    Human (12 healthy young males)
    plain_language
    Activated partial thromboplastin time was prolonged significantly at 2 and 4 h after the same single dose.
    primary_references
    A single-dose of oral nattokinase potentiates thrombolysis and anti-coagulation profiles. (2015) https://pubmed.ncbi.nlm.nih.gov/26109079/ DOI: 10.1038/srep11601
    route
    In vivo, oral
    tissue
    Plasma

    Nattokinase: what the purified enzyme cleaves, what survives being eaten, and the gap between the two (2026-09-23) · lines 895–895

    Original AI-assisted curation built from a supplied entity-first document of 105 entities and 129 claims. Every reference in that document was resolved against live PubMed with its abstract read and its DOI cross-checked on 2026-09-23, and the EFSA novel-food opinion was retrieved and read in full. That check corrected two PMIDs that pointed at unrelated papers, two DOIs, and two papers recorded as carrying no erratum that do carry one; it also reversed three findings the supplied document had stated backwards. Two papers carry a published correction, recorded as such and not as a retraction. Three sources are not indexed in PubMed and are cited by what they have. Laboratory lineages are recorded, so the four papers from one group, the three from another and the two readings of a single applicant dossier cannot be counted as separate lines of support. Study-specific doses, units, populations and limitations retained; activity units are never converted between systems. Not publisher full text. · supports · Human (12 healthy young males) · source_derived_draft · unverified_draft

    Activated partial thromboplastin time was prolonged significantly at 2 and 4 h after the same single dose.
    Complete structured claim and evidence
  2. Activated partial thromboplastin time also rose significantly more with nattokinase than with placebo over the same eight weeks.

    Experimental context and source evidence
    duration
    8 weeks
    evidence_access
    Primary PubMed abstract and indexed metadata reviewed. Full-text method details not stated here remain unresolved.
    experimental_model
    Human (100 nondiabetic hypercholesterolemic subjects)
    exposure
    Nattokinase, dose not stated in the abstract
    limitations
    Agrees in direction with the single-dose crossover finding at a different dose and duration. Same erratum note as above.
    organism
    Human (100 nondiabetic hypercholesterolemic subjects)
    plain_language
    Activated partial thromboplastin time also rose significantly more with nattokinase than with placebo over the same eight weeks.
    primary_references
    The effects of nattokinase supplementation on collagen-epinephrine closure time, prothrombin time and activated partial thromboplastin time in nondiabetic and hypercholesterolemic subjects. (2019) https://pubmed.ncbi.nlm.nih.gov/31070609/ DOI: 10.1039/c8fo02324g Correction on record: Erratum in: Food Funct. 2019 Jul 17;10(7):4454. doi: 10.1039/c9fo90033k. PMID 31287455.
    route
    In vivo, oral
    tissue
    Plasma

    Nattokinase: what the purified enzyme cleaves, what survives being eaten, and the gap between the two (2026-09-23) · lines 972–972

    Original AI-assisted curation built from a supplied entity-first document of 105 entities and 129 claims. Every reference in that document was resolved against live PubMed with its abstract read and its DOI cross-checked on 2026-09-23, and the EFSA novel-food opinion was retrieved and read in full. That check corrected two PMIDs that pointed at unrelated papers, two DOIs, and two papers recorded as carrying no erratum that do carry one; it also reversed three findings the supplied document had stated backwards. Two papers carry a published correction, recorded as such and not as a retraction. Three sources are not indexed in PubMed and are cited by what they have. Laboratory lineages are recorded, so the four papers from one group, the three from another and the two readings of a single applicant dossier cannot be counted as separate lines of support. Study-specific doses, units, populations and limitations retained; activity units are never converted between systems. Not publisher full text. · supports · Human (100 nondiabetic hypercholesterolemic subjects) · source_derived_draft · unverified_draft

    Activated partial thromboplastin time also rose significantly more with nattokinase than with placebo over the same eight weeks.
    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