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    PAPER LOW-DOClinical Trial2026

    Low-dose rapamycin and cerebral blood flow in cognitively normal middle-aged adults by APOE genotype (pilot)

    Cerebral blood flow rose >15% in APOE4 carriers (n=9) but not non-carriers (n=14); no placebo arm, 4 weeks, surrogate endpoint.

    Evidence

    4/10

    Emerging Evidence

    Sample

    23

    subjects

    Duration

    4 weeks

    study period

    Journal

    Journal of Cerebral Blood Flow & Metabolism

    Sep 2026

    01

    Full Abstract

    Single-arm pilot of rapamycin 1 mg/day for 4 weeks in cognitively normal adults aged 45-65, stratified by APOE4 status.

    02

    Key Findings

    1. 01

      CBF increased >15% across multiple regions in APOE4 carriers

    2. 02

      No significant CBF change in non-carriers

    3. 03

      Favourable metabolic/inflammatory shifts with minimal adverse events

    03

    Structured Methods

    Study Design
    Clinical Trial
    Sample Size
    23 subjects
    Study Duration
    4 weeks
    Methodology
    Open-label single-arm pilot, APOE-stratified
    Limitations
    No control arm; 9 carriers; 4-week duration; perfusion is a surrogate for cognition; sex-specific press claims not supported by the abstract.
    04

    Citations & References

    Cite this paper

    Unknown authors (2026). Low-dose rapamycin and cerebral blood flow in cognitively normal middle-aged adults by APOE genotype (pilot). Journal of Cerebral Blood Flow & Metabolism. https://doi.org/10.1177/0271678X261490342

    DOI

    10.1177/0271678X261490342

    Source

    Publisher

    Journal

    Journal of Cerebral Blood Flow & Metabolism

    05

    Indexing

    Topics

    rapamycinAPOE4neurovascular

    Interventions

    rapamycin
    PHS
    671
    / 1000
    T3
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