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假定的过氧化物酶体增殖物激活受体γ启动子中的新型变异及其与男性肥胖的关系。

Novel variants in the putative peroxisome proliferator-activated receptor {gamma} promoter and relationships with obesity in men.

作者信息

Larsen Thomas M, Larsen Lesli H, Torekov Signe K, Ek Jakob, Black Eva, Toubro Søren, Astrup Arne, Sørensen Thorkild I A, Hansen Torben, Pedersen Oluf

机构信息

Department of Human Nutrition, LMC Royal Veterinary and Agricultural University, Rolighedsvej 30, 1958 Frederiksberg C, Denmark.

出版信息

Obes Res. 2005 Jun;13(6):953-8. doi: 10.1038/oby.2005.110.

Abstract

Yet unidentified variants within the peroxisome proliferator-activated receptor gamma (PPARgamma) 2 promoter may explain the inconsistent reports on associations between variants in the coding region and obesity or diabetes. Thus, we examined the putative PPARgamma2 promoter (-3371 to +43 bp) for variants in 83 subjects with obesity or type 2 diabetes. We identified eight variants, seven of which were novel, including -792A>G, -816C>T, -882T>C, -1505G>A, -1881C>T, -1884T>A, -2604T>C, and -2953A>G. The variants -816C>T, -1505G>A, -1881C>T, and -2604T>C were in total linkage disequilibrium, and there was a high degree of linkage disequilibrium between several of the novel variants and Pro12Ala. The novel variants were, together with Pro12Ala and 1431C>T, examined for relationships with obesity among 234 men with early-onset obesity with a BMI at age approximately 20 years of 33.2+/-2.5 kg/m2 and 323 nonobese men with a BMI of 21.7+/-2.5 kg/m2, who were also reexamined after approximately 29 years. The prevalence of the identified variants was not significantly different between the two groups, and the variants did not affect changes in BMI over time. In conclusion, the identified novel variants in the PPARgamma2 promoter region do not explain the reported discrepancies in the association of previously identified variants with obesity and type 2 diabetes.

摘要

过氧化物酶体增殖物激活受体γ(PPARγ)2启动子区域内尚未明确的变异可能解释了关于编码区变异与肥胖或糖尿病之间关联的报道不一致的现象。因此,我们对83名肥胖或2型糖尿病患者的假定PPARγ2启动子(-3371至+43 bp)进行了变异检测。我们鉴定出8个变异,其中7个是新发现的,包括-792A>G、-816C>T、-882T>C、-1505G>A、-1881C>T、-1884T>A、-2604T>C和-2953A>G。变异-816C>T、-1505G>A、-1881C>T和-2604T>C完全处于连锁不平衡状态,并且几个新变异与Pro12Ala之间存在高度连锁不平衡。我们在234名早发性肥胖男性(年龄约20岁时BMI为33.2±2.5 kg/m²)和323名非肥胖男性(BMI为21.7±2.5 kg/m²)中检测了这些新变异以及Pro12Ala和1431C>T与肥胖的关系,这些男性在大约29年后也接受了重新检查。两组中鉴定出的变异患病率没有显著差异,并且这些变异不影响BMI随时间的变化。总之,在PPARγ2启动子区域鉴定出的新变异并不能解释先前报道的已鉴定变异与肥胖和2型糖尿病关联中的差异。

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