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A meta-analysis of the association between angiotensin-converting enzyme insertion/deletion gene polymorphism and end-stage renal disease risk in IgA nephropathy patients

机译:IgA肾病患者血管紧张素转化酶插入/缺失基因多态性和末期肾病风险的荟萃分析

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摘要

Background and objective: The association between angiotensin-converting enzyme (ACE) insertion/deletion (I/D) gene polymorphism and end-stage renal disease (ESRD) risk in IgA nephropathy (IgAN) patients is still controversial. A meta-analysis was performed to evaluate the association between ACE I/D gene polymorphism and ESRD susceptibility in IgAN patients. Method: A predefined literature search and selection of eligible relevant studies were performed to collect data from electronic databases. Results: Thirteen articles were identified for the analysis of the association between ACE I/D gene polymorphism and ESRD risk in IgAN patients. D allele and DD genotype were associated with ESRD susceptibility in IgAN patients for overall populations ( p =0.01 and 0.003, respectively). In Asians, there was a markedly positive association between DD genotype and ESRD susceptibility ( p =0.03). Furthermore, D allele and DD genotype were associated with ESRD susceptibility in Caucasians ( p =0.02 and 0.03, respectively). However, II genotype might not play a protective role against ESRD onset for overall populations, Asians and Caucasians. Conclusion: DD homozygote is a significant genetic molecular marker for the onset of ESRD in IgAN patients.
机译:背景和目的:IgA肾病(IgAn)患者的血管紧张素转换酶(ACE)插入/缺失(I / D)基因多态性和终末期肾病(ESRD)风险之间的关联仍存在争议。进行META分析以评估IGAN患者ACE I / D基因多态性和ESRD易感性之间的关联。方法:进行预定义的文献搜索和选择合格的相关研究,以收集来自电子数据库的数据。结果:IGAN患者ACE I / D基因多态性与ESRD风险与Ace I / D基因多态性与ESRD风险的关联分析。 D等位基因和DD基因型与IgAN患者的ESRD易感性有关,用于整体群体(P = 0.01和0.003)。在亚洲人中,DD基因型和ESRD易感性之间存在明显的阳性关联(P = 0.03)。此外,D等位基因和DD基因型与高加索人中的ESRD易感性有关(分别为0.02和0.03)。然而,II基因型可能不会对整个人群,亚洲人和高加索人的ESRD发作来发挥保护作用。结论:DD Homozygote是Igan患者ESRD发作的重要遗传分子标记。

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