A paired sibling analysis of the beta-3 adrenergic receptor and obesity in Mexican Americans

被引:86
作者
Mitchell, BD
Blangero, J
Comuzzie, AG
Almasy, LA
Shuldiner, AR
Silver, K
Stern, MP
MacCluer, JW
Hixson, JE
机构
[1] SW Fdn Biomed Res, Dept Genet, San Antonio, TX 78245 USA
[2] Univ Maryland, Dept Med, Dept Diabet Obes & Nutr, Baltimore, MD 21201 USA
[3] Johns Hopkins Univ, Dept Med, Div Endocrinol & Metab, Baltimore, MD 21287 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Med Epidemiol, San Antonio, TX 78284 USA
关键词
beta-3-adrenoreceptor; obesity; polymorphism; insulin resistance syndrome; genetics;
D O I
10.1172/JCI512
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The beta(3) adrenergic receptor, located on chromosome 8, is a regulator of energy expenditure acid lipolysis. A missense mutation in this gene, characterized by the replacement of tryptophan by arginine at codon 64 (Trp64Arg), is associated with obesity in some studies. We examined the effect of this variant on obesity in Mexican Americans, using a paired sibling design to minimize variability due to genetic background and a previously identified major susceptibility locus for obesity. We identified 45 sib-pairs that were concordant (identical by descent) for a locus on chromosome 2 which we have shown previously to be tightly linked to obesity in this population. The Trp64Arg variant, detected by PCR-restriction fragment length polymorphism analysis, was present in one sibling within each of the 45 sib-pairs. Presence of the variant was associated with significantly higher values in body mass index (P = 0.04), fat mass (P = 0.04), and waist circumference (P = 0.05). We conclude that the Trp64Arg variant is associated with obesity in this Mexican American population. The paired sibling design probably enhanced our ability to detect the effects of this variant by allowing us to account for variation attributable to another obesity susceptibility locus and to background genes.
引用
收藏
页码:584 / 587
页数:4
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