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

IF 4 Q1 CLINICAL NEUROLOGY
Huitong Ding, Chunyu Liu, Yi Li, Ting Fang Alvin Ang, Sherral Devine, Yulin Liu, Rhoda Au, P Murali Doraiswamy
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Abstract

The 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.

性别特异性血液生物标志物与中年人记忆力变化有关:弗雷明汉心脏研究
性别特异性血液生物标志物与中年人记忆力变化之间的关系仍不清楚。我们的目的是利用弗雷明汉心脏研究(FHS)的数据来研究这种关系。我们利用 FHS 后代队列中 793 名中年人(≤ 60 岁)的血液生物标志物和其他数据进行了关联分析、偏相关分析和因果剂量-反应曲线分析。结果显示,脂肪连素和空腹血糖与中年记忆力变化有关,高密度脂蛋白胆固醇与记忆力变化呈 U 型关系。其他血液生物标志物(如淀粉样 beta 蛋白 42)与记忆力变化没有明显关联。据我们所知,这是首次在前瞻性队列研究中对与中年记忆变化有关的血液生物标志物进行性别特异性网络分析。我们的研究结果突显了针对心脏代谢风险的重要性,以及验证中年特异性生物标志物的必要性,这些生物标志物可以加速初级预防策略的开发。
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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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