Evidence map›Paper›PMID 41723502›Full record

ArticleBiology of sex differences2026

Walking to protect against cognitive decline: the role of APOE genotype and sex.

Joel S Burma, Caterina Rosano, John R Best, Eleanor M Simonsick, Teresa Liu-Ambrose, Cindy K Barha

Abstract read
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Article in Biology of sex differences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Joel S BurmaBarha Brain Health Laboratory, Faculty of Kinesiology, University of Calgary, Calgary, AB, Canada.
Caterina RosanoSchool of Public Health, University of Pittsburgh, Pittsburgh, PA, USA.
John R BestDepartment of Gerontology, Simon Fraser University, Burnaby, BC, Canada.
Eleanor M SimonsickIntramural Research Program, National Institute on Aging, Baltimore, MD, USA.
Teresa Liu-AmbroseAging, Mobility, and Cognitive Neuroscience Laboratory, Department of Physical Therapy, University of British Columbia, Vancouver, BC, Canada.
Cindy K BarhaBarha Brain Health Laboratory, Faculty of Kinesiology, University of Calgary, Calgary, AB, Canada. Cindy.Barha@ucalgary.ca.

Funding

End of Life in the Very OldR01NR012459 · NINR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALBERT, STEVEN M, LUNNEY, JUNE R · 2011 to 2015
$2.7M
NINR NIH HHS R01 NR012459
6 · The paper itself

Abstract

backgroundThe apolipoprotein E (APOE) ε4 allele is a risk factor for late-onset Alzheimer's disease; however, risk varies by sex and lifestyle. Regular physical activity is known to mitigate cognitive decline; whether the degree of benefit differs by APOE genotype, sex, and race remains unknown.

methodsAnalyses utilized data from 2,985 participants in the Health, Aging, and Body Composition (HABC) cohort, comprising community-dwelling black and white older adults followed for 10 years. Cognitive performance was assessed multiple times across the 10 years using the Digit Symbol Substitution Test (DSST) for executive functions and processing speed and the Modified Mini-Mental State Examination (3MS) for global cognition. APOE genotypes were categorized into ε2, ε3, and ε4 groups. Annual self-reported walking time was used to quantify physical activity. Linear mixed models and latent growth curve modeling examined the interactions between APOE genotype, sex, and walking on cognitive trajectories with adjustments for race, study location, health score, age, education attained, and body mass index.

resultsAPOE ε4 carriers demonstrated steeper declines in both DSST and 3MS scores compared to ε3 carriers, irrespective of sex (all β<-0.13, all p < 0.004). APOE ε2 was protective longitudinally for 3MS in females only (β = 0.15, p < 0.002). Walking showed the strongest protective effect in APOE ε4 carriers for females and males in the rate of change of DSST and 3MS scores (all β > 0.27, all p < 0.044). DISCUSSION: These findings underscore the importance of public messaging about the benefits of regular physical activity for retaining cognitive function especially for persons genetically at heightened risk.

Indexed as

Apolipoproteins ECognitive DysfunctionSex CharacteristicsWalkingAgedAged, 80 and overCognitionFemaleGenotypeHumansMaleApolipoproteins EAPOE ε4Cognitive DeclinePhysical ActivitySex DifferencesWalking

Identifiers

PMID41723502
PMCPMC13032221

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.