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Genetic Susceptibility To Type 2 Diabetes: A Global Meta-Analysis Studying the Genetic Differences In Tunisian Populations

机译:对2型糖尿病的遗传易感性:全球荟萃分析研究突尼斯人群的遗传差异

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摘要

The present study is the first meta-analysis to evaluate type 2 diabetes (T2D) - associated polymorphisms in cohorts originated from several Tunisian regions. In fact, we evaluated the effect of seven polymorphisms in the following genes; PPARg ( Pro12Ala), TNFα (-308A/G), ENPP1(K121Q), TCF7L2(rs7903146 C/T), MTHFR( C677T), ACE(I/D), CAPN10(3R/2R) on T2D risk, through a meta-analysis combining data of previous studies performed on Tunisian populations originating from the north, centre or south of the country. R statistics version 2.12.1 software was used to estimate the heterogeneity between studies. Pooled ORs were computed by the fixed-effects method of Mantel-Haenszel if no heterogeneity between studies exists. Despite the similarities founded in a number of loci, the Woolf test reported that the contributions of ENPP1 and ACE loci in T2D risk are dependent on the geographic origin of concerned groups and this heterogeneity could be attributed not only, to the variable contribution of the variant in T2D risk, but also to diversities of genetic background between tested groups. Interestingly, observed heterogeneity highlighted founding concerning Y chromosome and the mitochondrial DNA about genetic structure of Tunisian population and proves once again that Tunisians, like the north- Africans, are a mosaic of subpopulations, with significant differences in genetic structure. In homogenous groups, we replicated the association of SNPs of TCF7L2, MTHFR, CAPN 10, TNFα and ACE genes with T2D risk in Tunisian population with OR ranging from 1.43 to 6.72. However, we reported an absence of association of PPARg with T2D in Tunisian population.
机译:本研究是首次评估来自多个突尼斯地区的人群中与2型糖尿病(T2D)相关的多态性的荟萃分析。实际上,我们评估了以下基因中七个多态性的作用。通过PPARg(Pro12Ala),TNFα(-308A / G),ENPP1(K121Q),TCF7L2(rs7903146 C / T),MTHFR(C677T),ACE(I / D),CAPN10(3R / 2R)通过T2D风险荟萃分析,结合先前对突尼斯人口(来自该国北部,中部或南部)进行的研究数据。使用R Statistics 2.12.1版软件估算研究之间的异质性。如果研究之间不存在异质性,则通过Mantel-Haenszel的固定效应方法计算合并的OR。尽管在多个基因座中存在相似之处,但Woolf检验报告说,ENPP1和ACE基因座​​在T2D风险中的贡献取决于相关人群的地理起源,并且这种异质性不仅可以归因于变异的可变贡献在T2D风险中,还影响了受测群体之间遗传背景的多样性。有趣的是,观察到的异质性突显了有关突尼斯人口遗传结构的Y染色体和线粒体DNA的发现,并再次证明突尼斯人像北非人一样,是亚种群的镶嵌体,遗传结构上存在显着差异。在同质组中,我们在突尼斯人群中复制了TCF7L2,MTHFR,CAPN 10,TNFα和ACE基因的SNP与T2D风险的关联,OR范围为1.43至6.72。然而,我们报道在突尼斯人口中缺乏PPARg与T2D的关联。

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