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血管紧张素转换酶插入/缺失基因多态性与终末期肾病易感性的关系。

Association between angiotensin-converting enzyme insertion/deletion gene polymorphism and end-stage renal disease susceptibility.

机构信息

Department of Pediatric Nephrology, The First Affiliated Hospital of GuangXi Medical University, China.

出版信息

J Renin Angiotensin Aldosterone Syst. 2014 Mar;15(1):22-31. doi: 10.1177/1470320312460898. Epub 2012 Oct 17.

DOI:10.1177/1470320312460898
PMID:23077080
Abstract

BACKGROUND AND OBJECTIVE

The association between angiotensin-converting enzyme (ACE) insertion/deletion (I/D) gene polymorphism and end-stage renal disease (ESRD) risk is still controversial. A meta-analysis was performed to evaluate the association between ACE I/D gene polymorphism and ESRD susceptibility.

METHOD

A predefined literature search and selection of eligible relevant studies were performed to collect data from electronic databases.

RESULTS

Thirty-four articles were identified for the analysis of an association between ACE I/D gene polymorphism and ESRD risk. Both D allele and DD genotype were associated with ESRD susceptibility in overall populations (D: OR = 1.20, 95% CI: 1.06-1.36, p = 0.003, DD: OR = 1.47, 95% CI: 1.20-1.78, p = 0.0001) and in East Asians (D: OR = 1.34, 95% CI: 1.06-1.69, p = 0.01, DD: OR = 2.01, 95% CI: 1.29-3.12, p = 0.002). Only the DD genotype had a positive association with ESRD susceptibility in Caucasians (OR = 1.20, 95% CI: 1.01-1.43, p = 0.03). The result from sensitivity analysis in overall populations or Caucasians was similar to those in non-sensitivity analysis, but not among East Asians.

CONCLUSIONS

The results of our study support the idea that D allele or DD genotype was associated with increased risk of ESRD susceptibility in the overall populations, and DD genotype was associated with ESRD susceptibility in Caucasians.

摘要

背景与目的

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。进行了一项荟萃分析,以评估 ACE I/D 基因多态性与 ESRD 易感性之间的关系。

方法

通过预设的文献搜索和合格相关研究的选择,从电子数据库中收集数据。

结果

共确定了 34 篇文章来分析 ACE I/D 基因多态性与 ESRD 风险之间的关系。在总体人群中,D 等位基因和 DD 基因型均与 ESRD 易感性相关(D:OR=1.20,95%CI:1.06-1.36,p=0.003,DD:OR=1.47,95%CI:1.20-1.78,p=0.0001)和东亚人群(D:OR=1.34,95%CI:1.06-1.69,p=0.01,DD:OR=2.01,95%CI:1.29-3.12,p=0.002)。只有 DD 基因型与高加索人群的 ESRD 易感性呈阳性相关(OR=1.20,95%CI:1.01-1.43,p=0.03)。在总体人群或高加索人群中的敏感性分析结果与非敏感性分析结果相似,但在东亚人群中则不然。

结论

我们的研究结果支持这样的观点,即 D 等位基因或 DD 基因型与 ESRD 易感性增加相关,在总体人群中,DD 基因型与高加索人群的 ESRD 易感性相关。

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