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血管紧张素转换酶I/D多态性与哮喘风险的关联:一项涉及11897名受试者的荟萃分析。

Association between angiotensin-converting enzyme I/D polymorphism and asthma risk: a meta-analysis involving 11,897 subjects.

作者信息

Ding Qun-Li, Sun Shi-Fang, Cao Chao, Deng Zai-Chun

机构信息

Department of Respiratory Medicine, Affiliated Hospital, Medicine College, Ningbo University, Ningbo, China.

出版信息

J Asthma. 2012 Aug;49(6):557-62. doi: 10.3109/02770903.2012.685540. Epub 2012 Jun 28.

DOI:10.3109/02770903.2012.685540
PMID:22741763
Abstract

BACKGROUND

Genetic susceptibility to asthma has been a research focus in the scientific community. Several studies have been conducted in recent years to evaluate the risk of asthma and insertion/deletion (I/D) polymorphism of angiotensin-converting enzyme (ACE). However, the results remain conflicting rather than conclusive.

METHODS

We carried out a search in Medline, EMBASE, and Chinese National Knowledge Infrastructure (CNKI) database for relevant studies. Data were extracted using a standardized form and pooled odds ratios (ORs) with 95% confidence intervals (CIs) were calculated to assess the strength of the association.

RESULTS

Our meta-analysis on 11,897 subjects from all available studies showed that the DD genotype was associated with increased asthma risk than those with the II (OR = 1.59, 95% CI = 1.20-2.12) or ID/II (OR = 1.62, 95% CI = 1.24-2.10) genotype. Stratified analyses by ethnicity (Europeans and Asians) and age (adults and children) obtained statistically similar results in the two genetic models. In the subgroup analysis by source of controls, the DD genotype was associated with a significantly elevated risk of asthma among population-based controls (DD vs. II: OR = 2.27, 95% CI = 1.45-3.56) but not hospital-based controls (DD vs. II: OR = 1.18, 95% CI = 0.93-1.49).

CONCLUSIONS

This meta-analysis provides strong evidence that the I/D polymorphism of ACE is associated with asthma risk. Additional well-designed large studies were required for the validation of our results, especially in African populations.

摘要

背景

哮喘的遗传易感性一直是科学界的研究重点。近年来开展了多项研究来评估哮喘风险与血管紧张素转换酶(ACE)插入/缺失(I/D)多态性之间的关系。然而,结果仍相互矛盾,尚无定论。

方法

我们在Medline、EMBASE和中国知网(CNKI)数据库中检索相关研究。使用标准化表格提取数据,并计算合并比值比(OR)及95%置信区间(CI)以评估关联强度。

结果

我们对所有现有研究中的11897名受试者进行的荟萃分析表明,与II型(OR = 1.59,95%CI = 1.20 - 2.12)或ID/II型(OR = 1.62,95%CI = 1.24 - 2.10)基因型相比,DD基因型与哮喘风险增加相关。按种族(欧洲人和亚洲人)和年龄(成年人和儿童)进行的分层分析在两种遗传模型中得到了统计学上相似的结果。在按对照来源进行的亚组分析中,DD基因型与基于人群的对照中哮喘风险显著升高相关(DD vs. II:OR = 2.27,95%CI = 1.45 - 3.56),但与基于医院的对照无关(DD vs. II:OR = 1.18,95%CI = 0.93 - 1.49)。

结论

这项荟萃分析提供了有力证据,表明ACE的I/D多态性与哮喘风险相关。需要更多设计良好的大型研究来验证我们的结果,尤其是在非洲人群中。

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