Component

Plasma ALCAR in human major depressive disorder

Plasma ALCAR in human major depressive disorder

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. Patients with major depressive disorder had lower plasma ALCAR in the 2018 case-control study.

    Experimental context and source evidence
    availability_state
    biomarker_context Imported condition classification; unverified.
    evidence_access
    Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    experimental_model
    71 MDD participants and 45 controls across two centers; observational human plasma measurements.
    interpretation_status
    Source-derived curation with stated access limits; ungraded, not independent replication.
    limitations
    Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation.
    nutrient_topic
    Acetyl-L-carnitine collection; exact intervention and molecular form govern interpretation. · Acetyl-L-carnitine
    plain_language
    Patients with major depressive disorder had lower plasma ALCAR in the 2018 case-control study.
    primary_references
    Acetyl-l-carnitine deficiency in patients with major depressive disorder. | https://pubmed.ncbi.nlm.nih.gov/30061399/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC6112703/ | https://doi.org/10.1073/pnas.1801609115
    source_locator
    Reviewed reference mdd-alcar-low; Exploratory severity, onset and treatment-resistance associations were reported. The study did not measure neuronal nuclear acetyl-CoA, Grm2 promoter acetylation or randomized supplementation response.
    trigger_kind
    biomarker_context Imported condition classification; unverified.

    Acetyl-L-carnitine: detailed mechanisms of action (reviewed 6 October 2026) · lines 571–577

    AI-assisted original review of primary studies and clearly identified official records. Exact primary access is stated; no independent replication is claimed. · supports · 71 MDD participants and 45 controls across two centers; observational human plasma measurements. · Recorded from source · Recorded from source

    ### mdd-alcar-low Patients with major depressive disorder had lower plasma ALCAR in the 2018 case-control study. Exploratory severity, onset and treatment-resistance associations were reported. The study did not measure neuronal nuclear acetyl-CoA, Grm2 promoter acetylation or randomized supplementation response. Model and exposure: 71 MDD participants and 45 controls across two centers; observational human plasma measurements. Limitations: Limited to the recorded preparation, model, exposure and endpoint. Does not establish a human dietary deficiency, clinical benefit or unique molecular mediation. Reference: Acetyl-l-carnitine deficiency in patients with major depressive disorder. | 2018 | https://pubmed.ncbi.nlm.nih.gov/30061399/ | https://pmc.ncbi.nlm.nih.gov/articles/PMC6112703/ | https://doi.org/10.1073/pnas.1801609115 | Access: Primary full text: relevant Results/Methods and figure descriptions reviewed; supplements only where explicitly stated.
    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.