认知障碍
载脂蛋白E
认知功能衰退
疾病
医学
阿尔茨海默病
肿瘤科
脑脊液
认知
队列
生物标志物
痴呆
生物
内科学
精神科
遗传学
作者
Francis Shue,Launia J. White,Rachel Hendrix,Jason D. Ulrich,Rachel L. Henson,William D. Knight,Yuka A. Martens,Ni Wang,Bhaskar Roy,Skylar C Starling,Yingxue Ren,Chengjie Xiong,Yan W. Asmann,Jeremy A. Syrjanen,Maria Vassilaki,Michelle M. Mielke,Jigyasha Timsina,Yun Ju Sung,Carlos Cruchaga,David M. Holtzman
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2024-04-03
卷期号:10 (14): eadk3674-eadk3674
被引量:21
标识
DOI:10.1126/sciadv.adk3674
摘要
The immune system substantially influences age-related cognitive decline and Alzheimer’s disease (AD) progression, affected by genetic and environmental factors. In a Mayo Clinic Study of Aging cohort, we examined how risk factors like APOE genotype, age, and sex affect inflammatory molecules and AD biomarkers in cerebrospinal fluid (CSF). Among cognitively unimpaired individuals over 65 ( N = 298), we measured 365 CSF inflammatory molecules, finding age, sex, and diabetes status predominantly influencing their levels. We observed age-related correlations with AD biomarkers such as total tau, phosphorylated tau-181, neurofilament light chain (NfL), and YKL40. APOE4 was associated with lower Aβ42 and higher SNAP25 in CSF. We explored baseline variables predicting cognitive decline risk, finding age, CSF Aβ42, NfL, and REG4 to be independently correlated. Subjects with older age, lower Aβ42, higher NfL, and higher REG4 at baseline had increased cognitive impairment risk during follow-up. This suggests that assessing CSF inflammatory molecules and AD biomarkers could predict cognitive impairment risk in the elderly.
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