Feng Zhitao, He Guochao, Chen Zhuanghong, Wu Zhengzhi, Li Juan
Department of Rheumatology, Nanfang Hospital, Southern Medical University, 1838 North of Guangzhou Road, Guangzhou, China.
BMC Musculoskelet Disord. 2014 Nov 18;15:376. doi: 10.1186/1471-2474-15-376.
Epidemiological studies have investigated the association between matrix metalloproteinase-3(MMP-3) gene-1171 5A/6A polymorphism and rheumatoid arthritis (RA), but the results were inconsistent. To evaluate the specific relationship, we performed a meta-analysis to clarify the controversies.
The relevant literatures dated to December 07th 2013 were retrieved from PubMed, EMBASE and the China National knowledge Infrastructure (CNKI) databases. The number of the alleles and genotypes for MMP-3 were obtained. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the association between MMP-3 5A/6A promoter polymorphism and RA. All of the statistical analyses were conducted by STATA11.0 software.
A total of 6 case-control studies covering 1451 cases and 1239 controls were included in the final meta-analysis. There was no significant association between MMP-3 5A/6A promoter polymorphism and RA in all genetic models (for 6A versus 5A: OR=1.19, 95% CI=0.91-1.56, P=0.203; 5A/6A versus 5A/5A: OR=1.31, 95% CI=0.89-1.92, P=0.174; 6A/6A versus 5A/5A: OR=1.78, 95% CI=0.68-4.61, P=0.238; the recessive model: OR=1.48, 95% CI=0.88-2.47, P=0.141; and the dominant model: OR=1.46, 95% CI=0.71-3.00, P=0.299). In the subgroup analysis by ethnicity, we obtained the similar results.
We systematically investigate the association between MMP-3-1171 5A/6A polymorphism and RA susceptibility; however, the results show a lack of correlation. Considering the small sample size and the selection bias existed in some studies, further studies are needed to confirm the findings.
流行病学研究已调查基质金属蛋白酶-3(MMP-3)基因-1171 5A/6A多态性与类风湿关节炎(RA)之间的关联,但结果不一致。为评估具体关系,我们进行了一项荟萃分析以澄清争议。
检索截至2013年12月7日的PubMed、EMBASE和中国知网(CNKI)数据库中的相关文献。获取MMP-3的等位基因和基因型数量。采用比值比(OR)和95%置信区间(CI)来估计MMP-3 5A/6A启动子多态性与RA之间的关联。所有统计分析均使用STATA11.0软件进行。
最终的荟萃分析共纳入6项病例对照研究,涵盖1451例病例和1239例对照。在所有遗传模型中,MMP-3 5A/6A启动子多态性与RA之间均无显著关联(6A与5A比较:OR = 1.19,95% CI = 0.91 - 1.56,P = 0.203;5A/6A与5A/5A比较:OR = 1.31,95% CI = 0.89 - 1.92,P = 0.174;6A/6A与5A/5A比较:OR = 1.78,95% CI = 0.68 - 4.61,P = 0.238;隐性模型:OR = 1.48,95% CI = 0.88 - 2.47,P = 0.141;显性模型:OR = 1.46,95% CI = 0.71 - 3.00,P = 0.299)。在按种族进行的亚组分析中,我们得到了相似的结果。
我们系统地研究了MMP-3 - 1171 5A/6A多态性与RA易感性之间的关联;然而,结果显示缺乏相关性。考虑到一些研究样本量较小且存在选择偏倚,需要进一步研究来证实这些发现。