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血管紧张素转化酶基因 I/D 多态性与哮喘风险的关系:荟萃分析。

The I/D polymorphism of angiotensin-converting enzyme gene and asthma risk: a meta-analysis.

机构信息

Department of Respiratory Medicine, West China Hospital of Sichuan University, Guoxuexiang 37, Chengdu, Sichuan, China.

出版信息

Allergy. 2011 Feb;66(2):197-205. doi: 10.1111/j.1398-9995.2010.02438.x. Epub 2010 Sep 29.

Abstract

BACKGROUND

The insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE) gene has been implicated in susceptibility to asthma, but a large number of studies have reported inconclusive results. The aim of this study is to investigate the association between the I/D polymorphism of ACE gene and asthma risk by meta-analysis.

METHODS

We searched Medline (Ovid), Pubmed, CNKI, Wanfang, and Weipu database, covering all papers until March 12, 2010. Statistical analysis was performed by using the software revman 4.2 (The Cochrane Collaboration, http://www.cochrane.org) and stata 10.0 (StataCorp, College Station, TX, USA, http://www.stata.com).

RESULTS

A total of 1946 cases and 2152 controls in 18 case-control studies were included in this meta-analysis. The results indicated that the DD homozygote carriers had a 59% increased risk of asthma, when compared with the homozygotes II and heterozygote DI [odds ratio (OR)=1.59, 95% confidence interval (CI): 1.16-2.18]. In the subgroup analysis by ethnicity, significant elevated risks were associated with DD homozygote carriers in Asians (OR=2.02 and 95% CI: 1.29-3.16 for DD vs DI+II) but not in Caucasians (OR=1.14 and 95% CI: 0.76-1.72 for DD vs DI+II). In the subgroup analysis by age, significant elevated risks were associated with DD homozygote carriers in children (OR=2.44 and 95% CI: 1.36-4.38 for DD vs II+DI) but not in adults (OR=1.54 and 95% CI: 0.94-2.51 for DD vs II+DI).

CONCLUSIONS

This meta-analysis suggested that the I/D polymorphism of ACE gene would be a risk factor of asthma. To further evaluate gene-to-gene and gene-to-environment interactions between polymorphisms of ACE gene and asthma risk, more studies with large groups of patients are required.

摘要

背景

血管紧张素转换酶(ACE)基因的插入/缺失(I/D)多态性与哮喘易感性有关,但大量研究结果尚无定论。本研究旨在通过荟萃分析探讨 ACE 基因 I/D 多态性与哮喘易感性的关系。

方法

我们检索了 Medline(Ovid)、Pubmed、中国知网(CNKI)、万方和维普数据库,检索时间截至 2010 年 3 月 12 日。采用 Revman 4.2 软件(The Cochrane Collaboration,http://www.cochrane.org)和 stata10.0(StataCorp,College Station,TX,USA,http://www.stata.com)进行统计学分析。

结果

共纳入 18 项病例对照研究的 1946 例病例和 2152 例对照。Meta 分析结果显示,DD 纯合子携带者患哮喘的风险增加 59%,与 II 纯合子和 DI 杂合子相比[比值比(OR)=1.59,95%可信区间(CI):1.16-2.18]。按种族亚组分析,亚洲人群中 DD 纯合子携带者哮喘风险显著增加(OR=2.02,95%CI:1.29-3.16 与 DI+II 相比),而白种人无此关联(OR=1.14,95%CI:0.76-1.72 与 DI+II 相比)。按年龄亚组分析,儿童组中 DD 纯合子携带者哮喘风险显著增加(OR=2.44,95%CI:1.36-4.38 与 II+DI 相比),而成年人无此关联(OR=1.54,95%CI:0.94-2.51 与 II+DI 相比)。

结论

本荟萃分析提示 ACE 基因 I/D 多态性可能是哮喘的危险因素。为进一步评估 ACE 基因多态性与哮喘易感性的基因-基因和基因-环境相互作用,还需要更多大样本的研究。

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