Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1HH, UK.
Hum Mol Genet. 2010 Mar 15;19(6):1129-36. doi: 10.1093/hmg/ddp561. Epub 2009 Dec 16.
The global prevalence of obesity has increased significantly in recent decades, mainly due to excess calorie intake and increasingly sedentary lifestyle. Here, we test the association between obesity measured by body mass index (BMI) and one of the best-known genetic variants showing strong selective pressure: the functional variant in the cis-regulatory element of the lactase gene. We tested this variant since it is presumed to provide nutritional advantage in specific physical and cultural environments. We genetically defined lactase persistence (LP) in 31 720 individuals from eight European population-based studies and one family study by genotyping or imputing the European LP variant (rs4988235). We performed a meta-analysis by pooling the beta-coefficient estimates of the relationship between rs4988235 and BMI from the nine studies and found that the carriers of the allele responsible for LP among Europeans showed higher BMI (P = 7.9 x 10(-5)). Since this locus has been shown to be prone to population stratification, we paid special attention to reveal any population substructure which might be responsible for the association signal. The best evidence of exclusion of stratification came from the Dutch family sample which is robust for stratification. In this study, we highlight issues in model selection in the genome-wide association studies and problems in imputation of these special genomic regions.
近几十年来,全球肥胖患病率显著上升,主要归因于卡路里摄入过多和日益久坐的生活方式。在这里,我们检测了通过身体质量指数(BMI)测量的肥胖与一种最知名的遗传变异之间的关联,这种遗传变异显示出强烈的选择压力:乳糖酶基因顺式调控元件中的功能性变异。我们选择检测这种变异,因为它被认为在特定的身体和文化环境中提供了营养优势。我们通过对来自八个欧洲基于人群的研究和一个家系研究的 31720 个人进行基因分型或推断欧洲乳糖持续存在(LP)的变体(rs4988235),在遗传上定义了 LP。我们通过合并九个研究中 rs4988235 与 BMI 之间关系的 beta 系数估计值,对该变体进行了荟萃分析,发现欧洲 LP 等位基因的携带者表现出更高的 BMI(P = 7.9 x 10(-5))。由于该基因座已显示出易受群体分层的影响,因此我们特别注意揭示可能导致关联信号的任何人口亚结构。来自荷兰家族样本的排除分层的最佳证据是稳健的。在这项研究中,我们强调了全基因组关联研究中模型选择的问题以及这些特殊基因组区域的推断问题。