首页> 外文期刊>The Tohoku Journal of Experimental Medicine >The -374A allele of the RAGE gene as a potential protective factor for vascular complications in type 2 diabetes: a meta-analysis.
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The -374A allele of the RAGE gene as a potential protective factor for vascular complications in type 2 diabetes: a meta-analysis.

机译:RAGE基因的-374A等位基因是2型糖尿病血管并发症的潜在保护因子:一项荟萃分析。

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The receptor for advanced glycation end products (RAGE) is a multi-ligand member of the immunoglobulin superfamily and may be involved in the development of diabetic vascular complications. The -374T/A polymorphism in the RAGE gene promoter has been suggested to affect gene transcription. However, the studies on the association between the -374T/A polymorphism and vascular complications in type 2 diabetes mellitus (T2DM) have rendered conflicting results. To shed light on these inconclusive findings, a meta-analysis of all eligible studies concerning this polymorphism was conducted. The PubMed and EMBASE databases were searched for relevant articles up to January 2010. Data on genotypes, allele frequencies and number of cases and controls were extracted. A pooled estimate of the genetic association, the heterogeneity between studies, the sensitivity for HWE (exclusion of studies not in Hardy-Weinberg equilibrium), and the publication bias were investigated. Nine articles with 3,799 cases and 4,899 controls were enrolled in the meta-analysis. The main analysis indicated significant heterogeneity and no association for the allele contrast [random effects odds ratio (RE OR) = 0.92 (0.83 approximately 1.02)]. However, sensitivity analysis for HWE diminished the heterogeneity and showed a marginal association [fixed effects OR = 0.92 (0.86 approximately 0.99)]. The comparison of AA genotype with TA+TT genotypes revealed significant results overall [RE OR = 0.70 (0.57 approximately 0.86)]. Subgroup analyses in Caucasians and macrovascualr disease also produced significant association. In conclusion, the -374A allele of the RAGE gene might be a protective factor for vascular complications in T2DM, especially in Caucasians and macrovascular disease.
机译:晚期糖基化终产物的受体(RAGE)是免疫球蛋白超家族的多配体成员,可能参与糖尿病血管并发症的发生。 RAGE基因启动子中的-374T / A多态性已被认为会影响基因转录。然而,有关-374T / A多态性与2型糖尿病(T2DM)血管并发症之间关系的研究得出了相互矛盾的结果。为了阐明这些不确定的发现,对所有与该多态性有关的合格研究进行了荟萃分析。检索截至2010年1月的PubMed和EMBASE数据库中的相关文章。提取有关基因型,等位基因频率以及病例和对照数量的数据。对遗传关联,研究之间的异质性,HWE的敏感性(排除不在Hardy-Weinberg平衡中的研究除外)和发表偏倚的汇总估计值进行了研究。荟萃分析纳入了9篇3,799例病例和4,899例对照的文章。主要分析表明,显着的异质性和等位基因对比没有关联[随机效应比值比(RE OR)= 0.92(0.83约1.02)]。但是,对HWE的敏感性分析减少了异质性,并显示了边际关联[固定效应OR = 0.92(0.86约为0.99)]。 AA基因型与TA + TT基因型的比较显示出显着的整体结果[RE OR = 0.70(0.57约0.86)]。高加索人和大血管疾病的亚组分析也产生了显着关联。总之,RAGE基因的-374A等位基因可能是T2DM中血管并发症的保护因素,尤其是在白种人和大血管疾病中。

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