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首页> 外文期刊>BMC Musculoskeletal Disorders >Lack of association of matrix metalloproteinase-3 gene polymorphism with susceptibility to rheumatoid arthritis: a meta-analysis
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Lack of association of matrix metalloproteinase-3 gene polymorphism with susceptibility to rheumatoid arthritis: a meta-analysis

机译:缺乏基质金属蛋白酶-3基因多态性与类风湿关节炎的关联性:一项荟萃分析

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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.
机译:流行病学研究调查了基质金属蛋白酶3(MMP-3)基因1171 5A / 6A多态性与类风湿关节炎(RA)的关联,但结果不一致。为了评估具体的关系,我们进行了荟萃分析以澄清争议。从PubMed,EMBASE和中国国家知识基础设施(CNKI)数据库中检索了日期为2013年12月7日的相关文献。获得了MMP-3的等位基因数目和基因型。赔率(OR)和95%置信区间(CI)用于估计MMP-3 5A / 6A启动子多态性与RA之间的关联。所有的统计分析均由STATA11.0软件进行。最终的荟萃分析共包括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之间均无显着关联(对于6A对5A:OR?=?1.19,95%CI?=?0.91-1.56,P?=?0.203; 5A / 6A对5A / 5A:OR?=?1.31,95%CI?=?0.89-1.92,P?=?0.174; 6A / 6A对5A / 5A: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;优势模型:OR == 1.46,95%CI == 0.71-3.00,Pα= 0.299)。在按种族进行的亚组分析中,我们获得了相似的结果。我们系统地研究了MMP-3-1171 5A / 6A多态性与RA敏感性之间的关联;然而,结果表明缺乏相关性。考虑到一些研究中样本量小且选择偏倚,需要进一步研究以确认发现。

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