载脂蛋白E
优势比
危险系数
人口
医学
人口学
疾病
老年学
遗传学
内科学
置信区间
生物
环境卫生
社会学
作者
Michaël E. Belloy,Shea J. Andrews,Yann Le Guen,Michael L. Cuccaro,Lindsay A. Farrer,Valerio Napolioni,Michael D. Greicius
出处
期刊:JAMA Neurology
[American Medical Association]
日期:2023-11-06
卷期号:80 (12): 1284-1284
被引量:142
标识
DOI:10.1001/jamaneurol.2023.3599
摘要
Apolipoprotein E (APOE)*2 and APOE*4 are, respectively, the strongest protective and risk-increasing, common genetic variants for late-onset Alzheimer disease (AD), making APOE status highly relevant toward clinical trial design and AD research broadly. The associations of APOE genotypes with AD are modulated by age, sex, race and ethnicity, and ancestry, but these associations remain unclear, particularly among racial and ethnic groups understudied in the AD and genetics research fields.
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