Division of Pulmonary Diseases, State Key Laboratory of Biotherapy of China, West China Hospital, West China School of Medicine, Sichuan University, Chengdu, Sichuan, China.
PLoS One. 2013;8(3):e60523. doi: 10.1371/journal.pone.0060523. Epub 2013 Mar 28.
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.
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.
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.
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.
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。
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)。
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。
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。