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Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project

机译:NHLBI-外显子组测序项目中的欧美裔女性与腰臀比例的罕见变异关联

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摘要

Waist-to-hip ratio (WHR), a relative comparison of waist and hip circumferences, is an easily accessible measurement of body fat distribution, in particular central abdominal fat. A high WHR indicates more intra-abdominal fat deposition and is an established risk factor for cardiovascular disease and type 2 diabetes. Recent genome-wide association studies have identified numerous common genetic loci influencing WHR, but the contributions of rare variants have not been previously reported. We investigated rare variant associations with WHR in 1510 European-American and 1186 African-American women from the National Heart, Lung, and Blood Institute-Exome Sequencing Project. Association analysis was performed on the gene level using several rare variant association methods. The strongest association was observed for rare variants in IKBKB (P=4.0 × 10−8) in European-Americans, where rare variants in this gene are predicted to decrease WHRs. The activation of the IKBKB gene is involved in inflammatory processes and insulin resistance, which may affect normal food intake and body weight and shape. Meanwhile, aggregation of rare variants in COBLL1, previously found to harbor common variants associated with WHR and fasting insulin, were nominally associated (P=2.23 × 10−4) with higher WHR in European-Americans. However, these significant results are not shared between African-Americans and European-Americans that may be due to differences in the allelic architecture of the two populations and the small sample sizes. Our study indicates that the combined effect of rare variants contribute to the inter-individual variation in fat distribution through the regulation of insulin response.
机译:腰臀比(WHR)是腰围和臀围的相对比较,是人体脂肪分布(尤其是腹部中央脂肪)的易于测量的指标。高WHR表示腹部内脂肪沉积更多,并且是心血管疾病和2型糖尿病的既定危险因素。最近的全基因组关联研究已经确定了许多影响WHR的常见遗传基因座,但是以前没有报道过稀有变异的贡献。我们调查了来自国家心脏,肺和血液研究所-外显子组测序项目的1510名欧美妇女和1186名非洲裔美国妇女与WHR的罕见变异关联。使用几种罕见的变异关联方法在基因水平上进行了关联分析。在欧美人中,IKBKB中的罕见变异(P = 4.0×10 -8 )观察到最强的关联,其中该基因的罕见变异预计会降低WHR。 IKBKB基因的激活涉及炎症过程和胰岛素抵抗,这可能会影响正常的食物摄入以及体重和体形。同时,先前发现COBLL1中稀有变异体的聚集(以前发现具有与WHR和空腹胰岛素相关的常见变异体)与欧美人中较高的WHR名义上相关(P = 2.23×10 -4 )。但是,非裔美国人和欧洲裔美国人之间并未共享这些重要结果,这可能是由于两个人群的等位基因结构存在差异以及样本量较小所致。我们的研究表明,稀有变异体的综合作用通过调节胰岛素反应而促进了脂肪分布的个体间变异。

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