期刊
NEUROBIOLOGY OF AGING
卷 123, 期 -, 页码 83-91出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2022.12.011
关键词
DNA methylation GrimAge; Sex; gender differences; Cognitive aging
Cognitive heterogeneity increases with age, making it difficult to identify sex differences. Comparisons of men and women on neuropsychological test performances showed no significant differences when matched by aging rates. However, women maintained their advantage in verbal learning and memory regardless of their aging rates, education, or depressive symptoms.
Cognitive heterogeneity increases with age rendering sex differences difficult to identify. Given estab-lished sex differences in biological aging, we examined whether comparisons of men and women on neuropsychological test performances differed as a function of age rate. Data were obtained from 1921 adults enrolled in the 2016 wave of the Health and Retirement Study. The residual from regressing the DNA methylation GrimAge clock on chronological age was used as the measure of aging rate. Slow and fast age rates were predefined as 1 standard deviation below or above the sex-specific mean rates, respec-tively. ANCOVAs were used to test group differences in test performances. Pairwise comparisons revealed that slow aging men outperformed fast aging women (and vice versa) on measures of executive func-tion/speed, visual memory and semantic fluency; however, when groups were matched by aging rates, no significant differences remained. In contrast, women, regardless of their aging rates, education or de-pressive symptoms maintained their advantage on verbal learning and memory. Implications for research on sex differences in cognitive aging are discussed.(c) 2022 Elsevier Inc. All rights reserved.
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