4.5 Article

Sex differences in plasma lipid profiles of accelerated brain aging

期刊

NEUROBIOLOGY OF AGING
卷 129, 期 -, 页码 178-184

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2023.05.013

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Lipids; Metabolomics; Brain aging; Plasma; Sex difference

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Lipids are important for brain structure and function, and studies show that men experience greater brain atrophy than women with aging. This study investigated the sex-specific associations between circulating lipids and brain atrophy in a sample of cognitively normal older adults. Results revealed sex differences in the associations between specific lipid profiles and accelerated brain aging. The findings suggest the need for further investigation into the mechanisms underlying these sex-specific lipid profiles.
Lipids are essential components of brain structure and shown to affect brain function. Previous studies have shown that aging men undergo greater brain atrophy than women, but whether the associations between lipids and brain atrophy differ by sex is unclear. We examined sex differences in the associations between circulating lipids by liquid chromatography-tandem mass spectrometry and the progression of MRI-derived brain atrophy index Spatial Patterns of Atrophy for Recognition of Brain Aging (SPARE-BA) over an average of 4.7 (SD = 2.3) years in 214 men and 261 women aged 60 or older who were initially cognitively normal using multivariable linear regression, adjusted for age, race, education, and baseline SPARE-BA. We found significant sex interactions for beta-oxidation rate, short-chain acylcarnitines, long-chain ceramides, and very long-chain triglycerides. Lower beta-oxidation rate and short-chain acylcarnitines in women and higher long-chain ceramides and very long-chain triglycerides in men were associated with faster increases in SPARE-BA (accelerated brain aging). Circulating lipid profiles of accelerated brain aging are sex-specific and vary by lipid classes and structure. Mechanisms underlying these sex-specific lipid profiles of brain aging warrant further investigation.Published by Elsevier Inc.

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