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UCP3基因启动子中的一种常见多态性及其与丹麦人群体重指数和长期体重变化的关系。

A prevalent polymorphism in the promoter of the UCP3 gene and its relationship to body mass index and long term body weight change in the Danish population.

作者信息

Dalgaard L T, Sørensen T I, Drivsholm T, Borch-Johnsen K, Andersen T, Hansen T, Pedersen O

机构信息

Steno Diabetes Center, DK-2820 Gentofte, Denmark.

出版信息

J Clin Endocrinol Metab. 2001 Mar;86(3):1398-402. doi: 10.1210/jcem.86.3.7301.

DOI:10.1210/jcem.86.3.7301
PMID:11238538
Abstract

Variability of the uncoupling protein 3 (UCP3) promoter has been associated with increased body mass index (BMI) and altered lipid profiles. Here we tested the hypothesis that variation of the UCP3 promoter is associated with either juvenile or maturity-onset obesity or body weight change over a 26-yr follow-up among Danish subjects. Mutation screening of approximately 1 kb 5' upstream of the UCP3 gene revealed one previously described -55 C-->T variant. The frequency of the polymorphism was evaluated by restriction fragment length polymorphism analysis in four groups of subjects: 1) a group of 744 obese Danish men who at the draft board examinations had a body mass index (BMI) of at least 31 kg/m(2), 2) a randomly selected control group consisting of 857 draftees, 3) 258 middle-aged subjects, and 4) 409 60-yr-old subjects. The frequency of the T allele was 26.0% (95% confidence interval, 23.8-28.2%) among the obese draftees and 26.9% (24.8-29.0%) in the control group (P = 0.6). The variant was not associated with BMI at a young age or with weight gain after a 26-yr follow-up. The frequency of the T allele was 29.5% (25.6-33.4%) in the middle-aged group and 25.8% (22.8-28.8%) among the 60-yr-old subjects. The polymorphism was not associated with increased BMI or percent body fat in these 2 groups. It is concluded that this variant does not play a major role in the development of common obesity among Danish subjects.

摘要

解偶联蛋白3(UCP3)启动子的变异性与体重指数(BMI)升高及血脂谱改变有关。在此,我们检验了这样一个假设,即UCP3启动子的变异与丹麦受试者中的青少年肥胖或成年期肥胖,或在26年随访期间的体重变化有关。对UCP3基因上游约1 kb的5'区域进行突变筛查,发现了一个先前描述的-55 C→T变异。通过限制性片段长度多态性分析评估了四组受试者中该多态性的频率:1)一组744名肥胖丹麦男性,他们在征兵体检时体重指数(BMI)至少为31 kg/m²;2)一个由857名应征者组成的随机选择的对照组;3)258名中年受试者;4)409名60岁受试者。肥胖应征者中T等位基因的频率为26.0%(95%置信区间,23.8 - 28.2%),对照组中为26.9%(24.8 - 29.0%)(P = 0.6)。该变异与年轻时的BMI或26年随访后的体重增加无关。中年组中T等位基因的频率为29.5%(25.6 - 33.4%),60岁受试者中为25.8%(22.8 - 28.8%)。该多态性与这两组中BMI升高或体脂百分比无关。结论是,在丹麦受试者中,这种变异在常见肥胖的发生发展中不发挥主要作用。

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