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释放线粒体解偶联蛋白 2(UCP2)启动子变异(G-866A;rs659366)与肥胖的关联:从病例对照研究到荟萃分析的步骤。

Unleash the Association of Mitochondrial Uncoupling Protein (UCP2) Promoter Variant (G-866A; rs659366) with Obesity: Stepping from a Case-Control Study to a Meta-analysis.

机构信息

Department of Biochemistry, Faculty of Science, Tanta University, Tanta, Egypt.

Genetic Unit, Children Hospital, Mansoura University, Mansoura, Egypt.

出版信息

Biochem Genet. 2020 Oct;58(5):738-770. doi: 10.1007/s10528-020-09973-y. Epub 2020 May 30.

DOI:10.1007/s10528-020-09973-y
PMID:32474746
Abstract

Numerous eligible articles investigated the potential impact of the promoter region of UCP2 (rs659366) variant and the susceptibility for obesity with questionable outcomes. Our team designed this case-control combined with meta-analysis survey to illustrate the contribution of this variant with obesity. This case-control survey was formulated based on 110 obese Egyptian patients and 122 non-obese controls. Genomic DNA was amplified for ascertaining of UCP2 (G-866A; rs659366) variant exploiting the PCR-RFLP technique. A literature search was completed to investigate the involvement of this variant with obesity from various genetic databases. In this case-control study, the distribution of UCP2 (rs659366) variant showed a significant association with obesity among Egyptian subjects under allelic and dominant models (P value = 0.0006 and < 0.001, respectively). Overall, twenty-five comparisons for this variant (8652 obese patients and 10,075 non-obese controls) were recruited in this meta-analysis survey. A noteworthy association of UCP2 (rs659366) variant with obesity was identified among Asians and Africans but not Caucasians under allelic, dominant as well as heterozygote models. Nevertheless, this meta-analysis could not accomplish a noticeable association with overall subjects under different genetic models. This case-controlled study revealed a robust association for UCP2 (rs659366) variant with obesity susceptibility in Egyptian subjects; however, this meta-analysis survey failed to achieve an association for this variant with obesity in overall subjects except among Asians and Africans.

摘要

许多符合条件的文章研究了 UCP2(rs659366)启动子区域变体的潜在影响及其对肥胖易感性的影响,但结果并不明确。我们的团队设计了这项病例对照研究,并结合荟萃分析来阐明该变体与肥胖的关系。这项病例对照研究基于 110 名肥胖埃及患者和 122 名非肥胖对照者。我们利用 PCR-RFLP 技术扩增基因组 DNA 以确定 UCP2(G-866A;rs659366)变体。我们还完成了文献检索,以从各种遗传数据库中调查该变体与肥胖的关系。在这项病例对照研究中,UCP2(rs659366)变体的分布在埃及人群中表现出与肥胖显著相关,无论是在等位基因还是显性模型下(P 值分别为 0.0006 和 <0.001)。总的来说,这项荟萃分析纳入了 25 项针对该变体的比较(8652 名肥胖患者和 10075 名非肥胖对照者)。在亚洲人和非洲人群中,UCP2(rs659366)变体与肥胖存在显著关联,但在白种人群中没有关联,无论是在等位基因、显性还是杂合子模型下。然而,在不同遗传模型下,该荟萃分析未能在总体人群中发现显著关联。这项病例对照研究表明,UCP2(rs659366)变体与埃及人群的肥胖易感性之间存在很强的关联;然而,这项荟萃分析未能在总体人群中发现该变体与肥胖的关联,除了在亚洲人和非洲人群中。

相似文献

1
Unleash the Association of Mitochondrial Uncoupling Protein (UCP2) Promoter Variant (G-866A; rs659366) with Obesity: Stepping from a Case-Control Study to a Meta-analysis.释放线粒体解偶联蛋白 2(UCP2)启动子变异(G-866A;rs659366)与肥胖的关联:从病例对照研究到荟萃分析的步骤。
Biochem Genet. 2020 Oct;58(5):738-770. doi: 10.1007/s10528-020-09973-y. Epub 2020 May 30.
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The frequent UCP2 -866G>A polymorphism protects against insulin resistance and is associated with obesity: a study of obesity and related metabolic traits among 17 636 Danes.UCP2-866G>A 多态性频繁发生可预防胰岛素抵抗,并与肥胖有关:对 17636 名丹麦人肥胖及相关代谢特征的研究。
Int J Obes (Lond). 2013 Feb;37(2):175-81. doi: 10.1038/ijo.2012.22. Epub 2012 Feb 21.
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The -866A/A genotype in the promoter of the human uncoupling protein 2 gene is associated with insulin resistance and increased risk of type 2 diabetes.人类解偶联蛋白2基因启动子中的-866A/A基因型与胰岛素抵抗及2型糖尿病风险增加相关。
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Association of uncoupling protein-2 -866G/A and Ala55Val polymorphisms with susceptibility to type 2 diabetes mellitus: A meta-analysis of case-control studies.解偶联蛋白-2 -866G/A 和 Ala55Val 多态性与 2 型糖尿病易感性的关联:病例对照研究的荟萃分析。
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Mol Genet Metab. 2007 Dec;92(4):351-8. doi: 10.1016/j.ymgme.2007.07.011. Epub 2007 Sep 17.
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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.UCP2 基因启动子-866G/A 多态性与德黑兰人群 2 型糖尿病和肥胖的关联研究:一项病例对照研究。
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Interaction between the UCP2 -866 G>A polymorphism, diabetes, and beta-blocker use among patients with acute coronary syndromes.UCP2-866G>A 多态性、糖尿病与急性冠脉综合征患者β受体阻滞剂应用之间的相互作用。
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The A allele of the UCP2 -866G/A polymorphism changes UCP2 promoter activity in HUVECs treated with high glucose.UCP2-866G/A 多态性的 A 等位基因改变了高糖处理的 HUVECs 中 UCP2 启动子的活性。
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