DNA methylation clocks and cognitive status among older adults in the US, NHANES 1999–2002

Biological aging, measured using DNA methylation, is a potential biomarker for cognitive health outcomes. We evaluated associations between DNA methylation clocks and cognition in a nationally representative sample of adults aged 60+ in the National Health and Nutrition Examination Survey (NHANES), 1999–2002. Genome-wide DNA methylation data were used to create 13 measures of biological aging trained on different aging phenotypes. Cognition was assessed with the Digit Symbol Substitution Test (DSST). To evaluate associations between each DNA methylation clock and DSST score, survey-weighted linear regression models adjusted for calendar age, sex, race/ethnicity, education, smoking, serum cotinine, and BMI were run. We assessed effect modification by sex, education, and race and ethnicity. Included participants (N = 1,463) were an average of 70.5 y old and 82.7% non-Hispanic White. The average DSST score was 46.9 (SD 17.6). Ten of 13 DNA methylation clocks were associated with DSST (adjusted p < 0.05). One year of GrimAge2 accelerated aging was associated with –0.41 points lower DSST score (95% CI: –0.61, –0.21; adjusted p = 5x10−4). In stratified analyses, higher magnitudes of association were observed among male and non-Hispanic White participants across multiple clocks. DNA methylation clocks may be a useful biomarker of cognitive status among older adults.

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Publication Details

Journal
Epigenetics Reports
Published
2025-12-12
DOI
https://doi.org/10.1080/28361512.2025.2599769
Primary Topic
Epigenetics and DNA Methylation
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article
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article

DNA methylation clocks and cognitive status among older adults in the US, NHANES 1999–2002

Epigenetics Reports
Epigenetics and DNA Methylation
article

DNA methylation clocks and cognitive status among older adults in the US, NHANES 1999–2002

article en

Abstract

Biological aging, measured using DNA methylation, is a potential biomarker for cognitive health outcomes. We evaluated associations between DNA methylation clocks and cognition in a nationally representative sample of adults aged 60+ in the National Health and Nutrition Examination Survey (NHANES), 1999–2002. Genome-wide DNA methylation data were used to create 13 measures of biological aging trained on different aging phenotypes. Cognition was assessed with the Digit Symbol Substitution Test (DSST). To evaluate associations between each DNA methylation clock and DSST score, survey-weighted linear regression models adjusted for calendar age, sex, race/ethnicity, education, smoking, serum cotinine, and BMI were run. We assessed effect modification by sex, education, and race and ethnicity. Included participants (N = 1,463) were an average of 70.5 y old and 82.7% non-Hispanic White. The average DSST score was 46.9 (SD 17.6). Ten of 13 DNA methylation clocks were associated with DSST (adjusted p < 0.05). One year of GrimAge2 accelerated aging was associated with –0.41 points lower DSST score (95% CI: –0.61, –0.21; adjusted p = 5x10−4). In stratified analyses, higher magnitudes of association were observed among male and non-Hispanic White participants across multiple clocks. DNA methylation clocks may be a useful biomarker of cognitive status among older adults.

Epigenetics ReportsVol. 3(1)
University of Michigan (US), Stanford University (US)
Openalex Percentile: Top 38%
Epigenetics and DNA Methylation
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