Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Arch Iran Med. 2010 Sep;13(5):384-90.
A functional polymorphism in the uncoupling protein 2 (UCP2) gene promoter has been associated with obesity and type 2 diabetes (T2D) in some populations. The impact of UCP2 polymorphisms on diabetes and obesity is still under debate. Contradictory results have been reported in different populations world-wide. To clarify the contribution of the UCP2 gene -866 G/A polymorphism in the Iranian population, we studied its association with obesity and T2D.
A total of 225 unrelated subjects were studied: 75 T2D patients without obesity, 75 obese patients without diabetes and 75 control subjects. The UCP2 -866 G/A polymorphism was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).
In the normal Iranian population, GG polymorphism was significantly associated with an increased HDL-C level (P=0.027). G/A polymorphism was not associated with obesity and T2D in our study population, but the odds ratio (OR) between GG and G/A polymorphism was 0.61 with a confidence interval (CI) range of 0.34 - 1.08 in obese patients. Subjects with AA genotypes in all of the studied groups showed a lower body mass index (BMI) than subjects with the GG genotype.
Although the data in our study population is not statistically significant, the A allele in the UCP2 gene promoter seems to be protective against obesity. This may suggest the possibility of UCP2 as a target molecule for studies on the etiology and treatment of obesity.
解偶联蛋白 2(UCP2)基因启动子中的功能多态性与一些人群中的肥胖和 2 型糖尿病(T2D)有关。UCP2 多态性对糖尿病和肥胖的影响仍存在争议。全球不同人群的报道结果存在矛盾。为了阐明 UCP2 基因-866G/A 多态性在伊朗人群中的作用,我们研究了其与肥胖和 T2D 的关系。
共研究了 225 名无关个体:75 名无肥胖的 T2D 患者、75 名无糖尿病的肥胖患者和 75 名对照。UCP2-866G/A 多态性通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定。
在正常伊朗人群中,GG 多态性与 HDL-C 水平升高显著相关(P=0.027)。在我们的研究人群中,G/A 多态性与肥胖和 T2D 无关,但肥胖患者中 GG 和 G/A 多态性之间的比值比(OR)为 0.61,置信区间(CI)范围为 0.34-1.08。所有研究组中 AA 基因型个体的体重指数(BMI)均低于 GG 基因型个体。
尽管我们研究人群的数据没有统计学意义,但 UCP2 基因启动子中的 A 等位基因似乎对肥胖具有保护作用。这可能表明 UCP2 作为肥胖病因学和治疗研究的靶分子的可能性。