Epigenetic Age Acceleration and Chronological Age: Associations With Cognitive Performance in Daily Life

Author:

Zavala Daisy V1ORCID,Dzikowski Natalie2,Gopalan Shyamalika3,Harrington Karra D4ORCID,Pasquini Giancarlo1ORCID,Mogle Jacqueline5ORCID,Reid Kerry26,Sliwinski Martin4ORCID,Graham-Engeland Jennifer E7,Engeland Christopher G7,Bernard Kristin1,Veeramah Krishna2,Scott Stacey B1ORCID

Affiliation:

1. Department of Psychology, Stony Brook University , Stony Brook, New York , USA

2. Department of Ecology and Evolution, Stony Brook University , Stony Brook, New York , USA

3. Department of Evolutionary Anthropology, Duke University , Durham, North Carolina , USA

4. Department of Human Development and Family Studies, The Pennsylvania State University , University Park, Pennsylvania , USA

5. Department of Behavioral, Social, and Health Sciences, Clemson University , Clemson, South Carolina , USA

6. Area of Ecology and Biodiversity, School of Biological Sciences, The University of Hong Kong , Hong Kong SAR , China

7. Department of Biobehavioral Health, The Pennsylvania State University , University Park, Pennsylvania , USA

Abstract

Abstract DNA methylation-derived epigenetic clocks offer the opportunity to examine aspects of age acceleration (ie, the difference between an individual’s biological age and chronological age), which vary among individuals and may better account for age-related changes in cognitive function than chronological age. Leveraging existing ambulatory cognitive assessments in daily life from a genetically diverse sample of 142 adults in midlife, we examined associations between 5 measures of epigenetic age acceleration and performance on tasks of processing speed and working memory. Covarying for chronological age, we used multilevel models to examine associations of epigenetic age acceleration (Horvath 1, Horvath 2, Hannum, PhenoAge, and GrimAge clocks) with both average level and variability of cognitive performance. Positive age acceleration (ie, epigenetic age greater than chronological age) was associated with poorer mean processing speed (Horvath 1 and 2) and working memory (GrimAge). Higher chronological age was also associated with poorer mean processing speed and working memory performance. Further, positive age acceleration was generally associated with greater intraindividual variability in working memory and processing speed tasks, whereas being chronologically older was associated with less intraindividual variability. Although further work is needed, our results indicate age acceleration effects have comparable or greater size as those for chronological age differences, suggesting that epigenetic age acceleration may account for additional risk and interindividual variation in cognitive performance above chronological age.

Funder

National Institutes of Health

National Institute on Aging

Stony Brook University

State University of New York

American Federation for Aging Research

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

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3. BioAge: toward a multi-determined, mechanistic account of cognitive aging;DeCarlo,2014

4. DNA methylation GrimAge strongly predicts lifespan and healthspan;Lu,2019

5. An epigenetic biomarker of aging for lifespan and healthspan;Levine,2018

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