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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.

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。

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