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欧洲裔 92105 名女性的肥胖遗传变异与初潮时间的关联。

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent.

机构信息

Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, 137 East Franklin Street, Suite 306, Campus Box 8050, Chapel Hill, NC 27514-8050, USA.

出版信息

Am J Epidemiol. 2013 Aug 1;178(3):451-60. doi: 10.1093/aje/kws473. Epub 2013 Apr 4.

Abstract

Obesity is of global health concern. There are well-described inverse relationships between female pubertal timing and obesity. Recent genome-wide association studies of age at menarche identified several obesity-related variants. Using data from the ReproGen Consortium, we employed meta-analytical techniques to estimate the associations of 95 a priori and recently identified obesity-related (body mass index (weight (kg)/height (m)(2)), waist circumference, and waist:hip ratio) single-nucleotide polymorphisms (SNPs) with age at menarche in 92,116 women of European descent from 38 studies (1970-2010), in order to estimate associations between genetic variants associated with central or overall adiposity and pubertal timing in girls. Investigators in each study performed a separate analysis of associations between the selected SNPs and age at menarche (ages 9-17 years) using linear regression models and adjusting for birth year, site (as appropriate), and population stratification. Heterogeneity of effect-measure estimates was investigated using meta-regression. Six novel associations of body mass index loci with age at menarche were identified, and 11 adiposity loci previously reported to be associated with age at menarche were confirmed, but none of the central adiposity variants individually showed significant associations. These findings suggest complex genetic relationships between menarche and overall obesity, and to a lesser extent central obesity, in normal processes of growth and development.

摘要

肥胖是全球关注的健康问题。女性青春期开始时间与肥胖之间存在着明确的反比关系。最近对初潮年龄的全基因组关联研究确定了几个与肥胖相关的变异。利用 ReproGen 联盟的数据,我们采用荟萃分析技术,对 38 项研究(1970 年至 2010 年)中 92116 名欧洲血统女性的 95 个先前确定的和最近确定的与肥胖相关的(体重(kg)/身高(m)(2)、腰围和腰臀比)单核苷酸多态性(SNP)与初潮年龄的关联进行了估计,以估计与中心或整体肥胖相关的遗传变异与女孩青春期时间之间的关联。每个研究的调查人员都使用线性回归模型对选定的 SNP 与初潮年龄(9-17 岁)之间的关联进行了单独分析,并调整了出生年份、地点(如适用)和人口分层。使用荟萃回归研究了效应量估计值的异质性。确定了与初潮年龄相关的 6 个新的体重指数位点的关联,并且确认了之前报道的与初潮年龄相关的 11 个肥胖相关位点,但没有一个中心肥胖变异体单独显示出显著的关联。这些发现表明,在正常的生长发育过程中,初潮和整体肥胖之间存在复杂的遗传关系,而在中心性肥胖方面的关系则较弱。

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