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首页> 外文期刊>Archives of Iranian medicine >Association study of the -866G/A UCP2 gene promoter polymorphism with type 2 diabetes and obesity in a Tehran population: a case control study.
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Association study of the -866G/A UCP2 gene promoter polymorphism with type 2 diabetes and obesity in a Tehran population: a case control study.

机译:德黑兰人口中-866G / A UCP2基因启动子多态性与2型糖尿病和肥胖的关联研究:病例对照研究。

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摘要

BACKGROUND: 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. METHODS: 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). RESULTS: 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. CONCLUSION: 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.
机译:背景:在一些人群中,解偶联蛋白2(UCP2)基因启动子的功能性多态性与肥胖症和2型糖尿病(T2D)有关。 UCP2多态性对糖尿病和肥胖的影响仍在争论中。在世界各地的不同人群中报告了矛盾的结果。为了阐明UCP2基因-866 G / A多态性在伊朗人群中的贡献,我们研究了其与肥胖症和T2D的关系。方法:共研究了225名无关受试者:75名无肥胖的T2D患者,75名无糖尿病的肥胖患者和75名对照受试者。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定UCP2 -866 G / A多态性。结果:在正常的伊朗人群中,GG多态性与HDL-C水平升高显着相关(P = 0.027)。在我们的研究人群中,G / A多态性与肥胖和T2D无关,但是,肥胖患者中GG与G / A多态性的比值比(OR)为0.61,置信区间(CI)范围为0.34-1.08。在所有研究组中,具有AA基因型的受试者的体重指数(BMI)均比具有GG基因型的受试者的体重指数低。结论: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等位基因似乎可以预防肥胖。这可能表明UCP2有可能成为肥胖病因和治疗研究的靶分子。

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