Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and Kidney Disease, National Institutes of Health Phoenix, Phoenix, Arizona, USA.
Obesity (Silver Spring). 2012 Dec;20(12):2426-30. doi: 10.1038/oby.2012.159. Epub 2012 Jun 22.
Genome-wide association studies (GWASs) have been used to search for susceptibility genes for type 2 diabetes and obesity in the Pima Indians, a population with a high prevalence of both diseases. In these studies, a variant (rs2025804) in the LEPR gene was nominally associated with BMI in 1,082 subjects (P = 0.03 adjusted for age, sex, birth year, and family membership). Therefore the LEPR and leptin overlapping transcript (LEPROT) genes were selected for further sequencing and genotyping in larger population-based samples for association analyses with obesity-related phenotypes. Selected variants (n = 80) spanning these genes were genotyped in a sample of full-heritage Pima Indians (n = 2,842) and several common variants including rs2025804 were nominally associated with BMI (P = 0.05-0.003 adjusted for age, sex, birth year, and family membership). Four common tag variants associated with BMI in the full-heritage Pima Indian sample were genotyped in a second sample of mixed-heritage Native Americans (n = 2,969) and three of the variants showed nominal replication (P = 0.03-0.006 adjusted as above and additionally for Indian heritage). Combining both samples provided the strongest evidence for association (adjusted P = 0.0003-0.0001). A subset of these individuals (n = 403) had been metabolically characterized for predictors of obesity and the BMI risk alleles for the variants tagged by rs2025804 were also associated with lower 24-h energy expenditure (24hEE) as assessed in a human respiratory chamber (P = 0.0007 adjusted for age, sex, fat mass, fat-free mass, activity, and family membership). We conclude that common noncoding variation in the LEPR gene is associated with higher BMI and lower energy expenditure in Native Americans.
全基因组关联研究(GWAS)已被用于在皮马印第安人群中搜索 2 型糖尿病和肥胖的易感基因,该人群这两种疾病的患病率都很高。在这些研究中,LEPR 基因中的一个变异(rs2025804)在 1082 名受试者中与 BMI 呈名义相关(调整年龄、性别、出生年份和家族成员后 P = 0.03)。因此,LEPR 和瘦素重叠转录物(LEPROT)基因被选为进一步测序和基因分型的对象,以在更大的基于人群的样本中进行与肥胖相关表型的关联分析。选择跨越这些基因的变异(n = 80)在全血统皮马印第安人样本(n = 2842)中进行基因分型,包括 rs2025804 在内的几种常见变异与 BMI 呈名义相关(调整年龄、性别、出生年份和家族成员后 P = 0.05-0.003)。在全血统皮马印第安人样本中与 BMI 相关的四个常见标签变异在混合血统的美洲原住民样本(n = 2969)中进行基因分型,其中三个变异显示出名义复制(调整后 P = 0.03-0.006,如上所述,另外还调整了印第安人血统)。将两个样本结合起来提供了最强的关联证据(调整后 P = 0.0003-0.0001)。这些个体的一个子集(n = 403)已经进行了代谢特征分析,以预测肥胖的预测因子,并且 rs2025804 标记的变异的 BMI 风险等位基因也与人类呼吸室评估的 24 小时能量消耗(24hEE)降低相关(调整年龄、性别、脂肪量、无脂肪量、活动和家族成员后 P = 0.0007)。我们得出结论,LEPR 基因中的常见非编码变异与美洲原住民的 BMI 较高和能量消耗较低有关。