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首页> 外文期刊>Journal of Renin-Angiotensin-Aldosterone System >A meta-analysis of the association between angiotensin-converting enzyme insertion/deletion gene polymorphism and end-stage renal disease risk in IgA nephropathy patients
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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换酶插入/缺失基因多态性与终末期肾脏疾病风险之间相关性的荟萃分析

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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:背景与目的:IgA肾病(IgAN)患者的血管紧张素转换酶(ACE)插入/缺失(I / D)基因多态性与终末期肾病(ESRD)风险之间的关联仍存在争议。进行荟萃分析以评估IgAN患者中ACE I / D基因多态性与ESRD易感性之间的关系。方法:进行预定义的文献检索和选择合格的相关研究,以从电子数据库中收集数据。结果:共鉴定出13篇文章,用于分析IgAN患者中ACE I / D基因多态性与ESRD风险之间的关系。 D等位基因和DD基因型与IgAN患者总人群的ESRD易感性相关(分别为p = 0.01和0.003)。在亚洲人中,DD基因型与ESRD易感性之间存在明显的正相关(p = 0.03)。此外,D等位基因和DD基因型与高加索人的ESRD易感性相关(分别为p = 0.02和0.03)。但是,II基因型可能不会对整个人群(亚洲人和高加索人)起ESRD起保护作用。结论:DD纯合子是IgAN患者ESRD发病的重要遗传分子标记。

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