Sex‐specific blood biomarkers linked to memory changes in middle‐aged adults: The Framingham Heart Study

Author:

Ding Huitong12,Liu Chunyu23,Li Yi3,Ang Ting Fang Alvin124,Devine Sherral12,Liu Yulin12,Au Rhoda12456,Doraiswamy P. Murali7

Affiliation:

1. Department of Anatomy and Neurobiology Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA

2. Framingham Heart Study Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA

3. Department of Biostatistics Boston University School of Public Health Boston Massachusetts USA

4. Slone Epidemiology Center Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA

5. Department of Neurology Boston University Chobanian & Avedisian School of Medicine Boston Massachusetts USA

6. Department of Epidemiology Boston University School of Public Health Boston Massachusetts USA

7. Neurocognitive Disorders Program Departments of Psychiatry and Medicine and the Duke Institute for Brain Sciences Duke University School of Medicine Durham North Carolina USA

Abstract

AbstractThe relationship between sex‐specific blood biomarkers and memory changes in middle‐aged adults remains unclear. We aimed to investigate this relationship using the data from the Framingham Heart Study (FHS). We conducted association analysis, partial correlation analysis, and causal dose–response curves using blood biomarkers and other data from 793 middle‐aged participants (≤ 60 years) from the FHS Offspring Cohort. The results revealed associations of adiponectin and fasting blood glucose with midlife memory change, along with a U‐shaped relationship of high‐density lipoprotein cholesterol with memory change. No significant associations were found for the other blood biomarkers (e.g., amyloid beta protein 42) with memory change. To our knowledge, this is the first sex‐specific network analysis of blood biomarkers related to midlife memory change in a prospective cohort study. Our findings highlight the importance of targeting cardiometabolic risks and the need to validate midlife‐specific biomarkers that can accelerate the development of primary preventive strategies.

Funder

National Institute on Aging

Publisher

Wiley

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