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基质金属蛋白酶-9-1562C/T 启动子多态性与 COPD 易感性相关:一项荟萃分析。

Matrix metalloproteinase-9 -1562C/T promoter polymorphism confers risk for COPD: a meta-analysis.

机构信息

Division of Pulmonary Diseases, State Key Laboratory of Biotherapy of China, West China Hospital, West China School of Medicine, Sichuan University, Chengdu, Sichuan, China.

出版信息

PLoS One. 2013;8(3):e60523. doi: 10.1371/journal.pone.0060523. Epub 2013 Mar 28.

Abstract

BACKGROUND

The role of matrix metalloproteinase (MMP) gene polymorphisms in the development of chronic obstructive pulmonary disease (COPD) has been reported with inconsistent results. This meta-analysis was performed to assess the association of MMP-1 -1607G/GG and MMP-9 -1562C/T promoter polymorphisms with COPD susceptibility.

METHODS

Published case-control studies from Pubmed and China National Knowledge Infrastructure (CNKI) databases were retrieved. Data were extracted and pooled odds ratios (OR) with 95% confidence intervals (CI) were calculated.

RESULTS

A total of fourteen case-control studies were included in this meta-analysis. Pooled effect size showed an association of MMP-9 -1562 C/T with the risk of COPD (dominant model: TT+CT vs CC; OR: 1.46; 95% CI: 1.02-2.08; p = 0.04). However, no correlation with COPD was revealed in MMP-1 -1607G/GG polymorphism. When stratified by ethnicity, results indicated MMP-1 -1607G/GG (recessive model: G/G vs G/GG+GG/GG; OR: 1.20; 95% CI: 1.01-1.44; p = 0.04) and MMP-9 -1562 C/T (dominant model; OR: 1.66; 95% CI: 1.01-2.71; p = 0.04) were correlated with COPD susceptibility among Caucasians and Asians respectively. According to source of controls, significant association of MMP-9 -1562 C/T (additive model: T vs C; OR:1.71, 95% CI: 1.42-2.07; p<0.00001, and dominant model; OR: 1.92; 95% CI: 1.34-2.76; p = 0.0004) with COPD susceptibility was revealed in the subgroup with smoker-based controls. However, in the aforementioned risk estimates, only the association of MMP-9 -1562 C/T (additive and dominant models) with the risk of COPD in the subgroup with smoker-based controls persisted significantly after Bonferroni correction for multiple testing. Moreover, after excluding the studies without Hardy-Weinberg equilibrium and/or with small sample size, the pooled results were robust and no publication bias was found in this study.

CONCLUSION

This meta-analysis suggests, when using healthy smokers as controls, MMP-9 -1562 C/T, but not MMP-1 -1607 G/GG polymorphism is associated with the risk of COPD.

摘要

背景

基质金属蛋白酶(MMP)基因多态性在慢性阻塞性肺疾病(COPD)的发展中的作用已有报道,但结果不一致。本荟萃分析旨在评估 MMP-1-1607G/GG 和 MMP-9-1562C/T 启动子多态性与 COPD 易感性的关系。

方法

从 Pubmed 和中国国家知识基础设施(CNKI)数据库中检索已发表的病例对照研究。提取数据并计算合并优势比(OR)及其 95%置信区间(CI)。

结果

本荟萃分析共纳入 14 项病例对照研究。合并效应大小显示 MMP-9-1562C/T 与 COPD 风险相关(显性模型:TT+CT 与 CC;OR:1.46;95%CI:1.02-2.08;p=0.04)。然而,MMP-1-1607G/GG 多态性与 COPD 无关。按种族分层,结果表明 MMP-1-1607G/GG(隐性模型:G/G 与 G/GG+GG/GG;OR:1.20;95%CI:1.01-1.44;p=0.04)和 MMP-9-1562C/T(显性模型;OR:1.66;95%CI:1.01-2.71;p=0.04)与高加索人和亚洲人 COPD 的易感性相关。根据对照来源,MMP-9-1562C/T(加性模型:T 与 C;OR:1.71,95%CI:1.42-2.07;p<0.00001,和显性模型;OR:1.92;95%CI:1.34-2.76;p=0.0004)与 COPD 易感性的显著相关性仅在吸烟者为对照的亚组中显示。然而,在上述风险估计中,仅 MMP-9-1562C/T(加性和显性模型)与吸烟者为对照的亚组中 COPD 风险的相关性在经过多次检验的 Bonferroni 校正后仍然显著。此外,在排除不符合 Hardy-Weinberg 平衡和/或样本量较小的研究后,本研究的汇总结果仍然稳健,且未发现发表偏倚。

结论

本荟萃分析表明,当使用健康吸烟者作为对照时,MMP-9-1562C/T,但不是 MMP-1-1607G/GG 多态性与 COPD 的风险相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c48/3610819/09caa4720f18/pone.0060523.g001.jpg

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