两个独立高加索人群中TNFR2基因CA重复多态性与肥胖表型的连锁和关联

HUANG Qing-Yang , SHEN Hui , DENG Hong-Yi , Theresa Conway , Leo Elze , K. Michael Davies , Robert R. Recker , DENG Hong-Wen
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引用次数: 1

摘要

本课题组此前报道了1p36与身体质量指数(BMI) (LOD = 2.09)的关联证据。肿瘤坏死因子受体2 (TNFR2)位于1p36,是一个很好的定位和功能的肥胖候选基因。在这项研究中,我们使用定量传递不平衡测试(QTDT)在两个大型独立样本中研究了TNFR2基因与肥胖表型之间的联系和关联。第一组由来自79个多代谱系的1836个个体组成。第二组是随机确定的来自157个美国高加索核心家庭的636个人。肥胖表型测试包括BMI、脂肪量和脂肪量百分比(PFM)。在多代谱系样本中,观察到与BMI的关联显著结果(P = 0.0056)。我们的数据支持TNFR2基因作为高加索人群BMI变异的数量性状位点(QTL)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Linkage and Association Between CA Repeat Polymorphism of the TNFR2 Gene and Obesity Phenotypes in Two Independent Caucasian Populations

Previously, our group has reported a suggestive linkage evidence of 1p36 with body mass index (BMI) (LOD = 2.09). The tumor necrosis factor receptor 2 (TNFR2) at 1p36 is an excellent positional and functional candidate gene for obesity. In this study, we have investigated the linkage and association between the TNFR2 gene and obesity phenotypes in two large independent samples, using the quantitative transmission disequilibrium tests (QTDT). The first group was made up of 1 836 individuals from 79 multi-generation pedigrees. The second group was a randomly ascertained set of 636 individuals from 157 US Caucasian nuclear families. Obesity phenotypes tested include BMI, fat mass, and percentage fat mass (PFM). A significant result (P = 0.0056) was observed for linkage with BMI in the sample of the multigenerational pedigrees. Our data support the TNFR2 gene as a quantitative trait locus (QTL) underlying BMI variation in the Caucasian populations.

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