GW24-e2207 Association between--1562 C>T polymorphism in the promoter region of matrix metalloproteinase-9 (MMP-9) and coronary artery disease: A meta-analysis
Guan Weiwei Chenken, Hongmei Ren, Lin Zhou, Chunyu Zeng
Abstract
Guan Weiwei Chenken, Hongmei Ren, Lin Zhou, Chunyu Zeng
Abstract
Objectives To determine the association between-1562 C>T polymorphism in the promoter region of matrix metalloproteinase-9 (MMP-9) and coronary artery disease (CAD) risk. Methods This meta-analysis was on the basis of 26 studies including 12,776 cases and 6,371 controls. The was assessed by the Q-statistic test and the I2-statistic test. Sensitivity analysis was conducted by sequentially omitting any single study and recalculating the ORs and 95% CIs. Funnel plots and Egger’s test were performed to test the potential publication bias. All the data were analysed by using STATA version 12.0. Results We found that-1562 C>T polymorphism did not contribute to susceptibility to CAD in the overall results (ORCC vs. TT= 0.99, 95% CI = 0.94-1.04, P heterogeneity= 1.000; ORCC + CT vs. TT = 0.99, 95% CI = 0.95-1.04, P heterogeneity= 1.000; ORCC vs. CT + TT= 0.96, 95% CI = 0.92-1.01, P heterogeneity= 0.992; ORallele C vs. allele T= 0.98, 95% CI = 0.95-1.01, P heterogeneity= 1.000; ORCT vs. TT= 0.98, 95% CI = 0.89-1.07, P heterogeneity = 1.000). But the stratified analysis by ethnicity and source of control indicated-1562 C>T polymorphism may be a risk factor for the CAD risk in Asians and hospital populations. Conclusions Our meta-analysis supported the fact that-1562 C>T polymorphism was not associated with the susceptibility to CAD. Further larger studies are required to confirm our findings.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objectives To determine the association between-1562 C>T polymorphism in the promoter region of matrix metalloproteinase-9 (MMP-9) and coronary artery disease (CAD) risk. Methods This meta-analysis was on the basis of 26 studies including 12,776 cases and 6,371 controls. The was assessed by the Q-statistic test and the I2-statistic test. Sensitivity analysis was conducted by sequentially omitting any single study and recalculating the ORs and 95% CIs. Funnel plots and Egger’s test were performed to test the potential publication bias. All the data were analysed by using STATA version 12.0. Results We found that-1562 C>T polymorphism did not contribute to susceptibility to CAD in the overall results (ORCC vs. TT= 0.99, 95% CI = 0.94-1.04, P heterogeneity= 1.000; ORCC + CT vs. TT = 0.99, 95% CI = 0.95-1.04, P heterogeneity= 1.000; ORCC vs. CT + TT= 0.96, 95% CI = 0.92-1.01, P heterogeneity= 0.992; ORallele C vs. allele T= 0.98, 95% CI = 0.95-1.01, P heterogeneity= 1.000; ORCT vs. TT= 0.98, 95% CI = 0.89-1.07, P heterogeneity = 1.000). But the stratified analysis by ethnicity and source of control indicated-1562 C>T polymorphism may be a risk factor for the CAD risk in Asians and hospital populations. Conclusions Our meta-analysis supported the fact that-1562 C>T polymorphism was not associated with the susceptibility to CAD. Further larger studies are required to confirm our findings.
Key concepts: Medicine, Meta-analysis, Internal medicine, Publication bias, Funnel plot, Coronary artery disease, Allele, Gastroenterology