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Cognition and Brain Health

Subjective memory in adults over 50 years of age: associations with affective and physiological markers of emotion regulation

, , , , &
Pages 971-979 | Received 03 Nov 2020, Accepted 13 Mar 2021, Published online: 30 Mar 2021
 

Abstract

Objectives

To examine associations among subjective memory reports, psychophysiological markers of emotion regulation, and cognitive performance in healthy adults over 50 years of age.

Method

A cross-sectional laboratory study was conducted with healthy, community-dwelling, non-depressed adults (M age = 60.4 years, SD = 8.4). The Metamemory in Adulthood (MIA) questionnaire provided reports of subjective memory capacity and stability (versus decline) and anxiety about memory. Poorer emotion regulation was marked by greater negative affect (NA) and lower high frequency heart rate variability (HF-HRV) responses to a challenging working memory task. Regression models were used to identify associations between subjective memory and emotion regulation markers, and structural equation modeling was used to explore whether emotion regulation mediated associations between subjective memory and objective task performance.

Results

A total of 115 participants were included in the final sample. Subjective memory decline (indicated by lower scores on memory stability) was associated with lower HF-HRV response and worse working memory performance. Poorer subjective memory capacity and more anxiety about memory were both associated with greater negative affect in response to the working memory task. There was an indirect effect of subjective memory capacity on working memory performance through negative affect response.

Conclusions

The findings here suggest that worse subjective memory may signal reduced capacity for emotion regulation. Along with known cognitive risks of depression and anxiety, more subtle emotion regulation difficulties may be involved in pathways of poor cognitive aging.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

The research was supported by NIH/National Institute on Aging under grant R03 AG030029 and a research supplement to promote diversity in health-related research to parent award R01 AG049764.

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