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Association of matrix metalloproteinase-9 C1562T polymorphism and coronary artery disease: a meta-analysis

机译:基质金属蛋白酶9 C1562T多态性与冠状动脉疾病的关联:一项荟萃分析

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摘要

Objective: Many investigations have studied the associations between matrix metalloproteinase-9 (MMP-9) C1562T polymorphisms and coronary artery disease (CAD). However, the conclusions of these studies were inconsistent. Therefore, this study was aimed at clarifying the association between MMP-9 C1562T polymorphisms and CAD in a large-scale meta-analysis. Methods: The PubMed and Embase databases were retrieved to collect all publications on the association between MMP-9 C1562T polymorphisms and CAD. Then the odd ratios (ORs) and 95% confidence intervals (95% CIs) for C1562T TT+TC versus CC genotype between CAD and the control groups were evaluated. Subgroup analysis was also performed according to different races. The meta-analysis was performed by Stata 10.0. Results: Sixteen case-control studies were included in our meta-analysis, involving 11 032 CAD patients and 4628 non-CAD controls. Compared with C allele carriers, East Asian T allele carriers TT+TC had a significantly higher risk of CAD (OR=1.43; 95% CI: 1.03–1.99; P=0.031); however, there were no significant associations in Western populations (OR=1.06; 95% CI: 0.96–1.18; P=0.240) or West Asians (OR=1.13; 95% CI: 0.75–1.70; P=0.565). When further analyzing the association between C1562T polymorphisms and myocardial infarction (MI, the most serious type of CAD), the risk of TT+TC genotype versus CC genotype for MI was significantly higher for the overall (OR=1.21; 95% CI: 1.04–1.40; P=0.012) and for East Asians (OR=1.58; 95% CI: 1.26–1.97; P=0.000) but not in Western populations (OR=1.12; 95% CI: 0.99–1.26; P=0.078). Conclusions: Our meta-analysis suggested an obvious ethnic difference in the association between MMP-9 C1562T polymorphisms and CAD. MMP-9 C1562T polymorphism was significantly related to CAD in East Asians. However, no significant associations were observed in either West Asians or Western populations.
机译:目的:许多研究已经研究了基质金属蛋白酶9(MMP-9)C1562T多态性与冠心病(CAD)的关联。但是,这些研究的结论不一致。因此,本研究旨在在大规模荟萃分析中阐明MMP-9 C1562T多态性与CAD之间的关联。方法:检索PubMed和Embase数据库以收集有关MMP-9 C1562T多态性与CAD之间关联的所有出版物。然后评估CAD和对照组之间C1562T TT + TC与CC基因型的奇数比(OR)和95%置信区间(95%CI)。还根据不同种族进行了亚组分析。荟萃分析由Stata 10.0执行。结果:我们的荟萃分析包括16项病例对照研究,涉及11032名CAD患者和4628名非CAD对照。与C等位基因携带者相比,东亚T等位基因携带者TT + TC具有显着更高的CAD风险(OR = 1.43; 95%CI:1.03-1.99; P = 0.031);然而,在西方人群(OR = 1.06; 95%CI:0.96-1.18; P = 0.240)或西亚亚裔(OR = 1.13; 95%CI:0.75-1.70; P = 0.565)之间没有显着的相关性。当进一步分析C1562T基因多态性与心肌梗死(MI,最严重的CAD类型)之间的关联时,总体而言,MI的TT + TC基因型与CC基因型的风险在总体上显着更高(OR = 1.21; 95%CI:1.04) –1.40; P = 0.012)和东亚人(OR = 1.58; 95%CI:1.26-1.97; P = 0.000),但在西方人群中则没有(OR = 1.12; 95%CI:0.99-1.26; P = 0.078) 。结论:我们的荟萃分析表明MMP-9 C1562T多态性与CAD之间存在明显的种族差异。 MMP-9 C1562T多态性与东亚人的CAD显着相关。但是,在西亚人或西方人群中均未发现明显的关联。

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