Genetic profile may make low-dose aspirin cut dementia risk by 70%
A study of ASPREE trial participants found that older adults with a certain platelet-related genetic makeup who took low-dose aspirin had about a 70% lower relative risk of dementia, but they also faced higher rates of major bleeding.
An analysis of the ASPREE trial, which enrolled over 13,500 elderly participants, revealed that low-dose aspirin may dramatically lower dementia risk for a subset of people with specific genetic variants linked to higher platelet counts. In the highest quintile of platelet-count polygenic scores, only 1% of aspirin users developed dementia versus 3.3% of those on placebo, indicating a roughly 70% relative risk reduction.
The benefit came with a notable safety trade-off: major bleeding occurred in 4.4% of aspirin users compared with 2.1% on placebo within the same genetic group. The study, published in Alzheimer's & Dementia, suggests that genetic screening could eventually identify individuals who might profit from aspirin as a preventive measure. Nonetheless, the authors stress that the findings must be replicated in other cohorts and tested in a trial designed for this genetic profile before any changes to medical guidance. They also warn against self-medicating with aspirin without professional advice due to the bleeding risk.
Why it matters
If confirmed, genetic testing could enable personalized aspirin use to prevent dementia, but safety concerns demand careful validation.
In this story
