Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE

生命银行 医学 肥胖 全基因组关联研究 遗传关联 等位基因 载脂蛋白E 生物信息学 内科学 遗传学 生物 单核苷酸多态性 基因型 基因 疾病
作者
Yann C. Klimentidis,David A. Raichlen,Jennifer W. Bea,David O. Garcia,Nathan E. Wineinger,Lawrence J. Mandarino,Gene E. Alexander,Zhao Chen,Scott B. Going
出处
期刊:International Journal of Obesity [Springer Nature]
卷期号:42 (6): 1161-1176 被引量:328
标识
DOI:10.1038/s41366-018-0120-3
摘要

Physical activity (PA) protects against a wide range of diseases. Habitual PA appears to be heritable, motivating the search for specific genetic variants that may inform efforts to promote PA and target the best type of PA for each individual. We used data from the UK Biobank to perform the largest genome-wide association study of PA to date, using three measures based on self-report (nmax = 377,234) and two measures based on wrist-worn accelerometry data (nmax = 91,084). We examined genetic correlations of PA with other traits and diseases, as well as tissue-specific gene expression patterns. With data from the Atherosclerosis Risk in Communities (ARIC; n = 8,556) study, we performed a meta-analysis of our top hits for moderate-to-vigorous PA (MVPA). We identified ten loci across all PA measures that were significant in both a basic and a fully adjusted model (p < 5 × 10−9). Upon meta-analysis of the nine top hits for MVPA with results from ARIC, eight were genome-wide significant. Interestingly, among these, the rs429358 variant in the APOE gene was the most strongly associated with MVPA, whereby the allele associated with higher Alzheimer’s risk was associated with greater MVPA. However, we were not able to rule out possible selection bias underlying this result. Variants in CADM2, a gene previously implicated in obesity, risk-taking behavior and other traits, were found to be associated with habitual PA. We also identified three loci consistently associated (p < 5 × 10−5) with PA across both self-report and accelerometry, including CADM2. We found genetic correlations of PA with educational attainment, chronotype, psychiatric traits, and obesity-related traits. Tissue enrichment analyses implicate the brain and pituitary gland as locations where PA-associated loci may exert their actions. These results provide new insight into the genetic basis of habitual PA, and the genetic links connecting PA with other traits and diseases.
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