Abstract

Objective Current findings on the association between MMP-9 rs3918242 and susceptibility to myocardial infarction (MI) are inconsistent, and their definite relationship is discussed in this meta-analysis. Methods Eligible literatures reporting MMP-9 rs3918242 and susceptibility to MI were searched in PubMed, Cochrane Library, CNRI, and VIP using keywords such as “MMP-9”, “matrix metallopeptidase-9” and “myocardial infarction”, “acute myocardial infarction”, “AMI”, and “polymorphism”. Data from eligible literatures were extracted for calculating OR and corresponding 95% CI using RevMan 5.3 and STATA12.0. Results Ten independent literatures reporting MMP-9 rs3918242 and susceptibility to MI were enrolled. Compared with subjects carrying CT&TT genotype of MMP-9 rs3918242, susceptibility to MI was lower in those carrying CC genotype (OR = 1.49, 95%CI = 1.19–1.86, P = 0.0004). Such a significance was observed in the overdominant (OR = 1.27, 95%CI = 1.14–1.41, P < 0.0001) and allele genetic models (OR = 1.43, 95%CI = 1.17–1.74, P = 0.0005) as well. This finding was also valid in the Asian population. Conclusions Mutation on MMP-9 rs3918242 has a potential relevance with susceptibility to MI.

Highlights

  • Acute myocardial infarction (AMI) manifests as myocardial necrosis which resulted from acute, persistent ischemia and hypoxia in the coronary arteries

  • Current researches have defined that interactions between various environmental factors and certain genetic polymorphisms may lead to AMI [4, 5]

  • Eligible literatures reporting MMP9 rs3918242 and susceptibility to MI published before May 2019 were searched in PubMed, Cochrane Library, CNRI, and VIP

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Summary

Introduction

Acute myocardial infarction (AMI) manifests as myocardial necrosis which resulted from acute, persistent ischemia and hypoxia in the coronary arteries. More than 800,000 AMI cases each year are newly onset, and 27% of them die before arriving at the hospital [1]. The incidence of AMI has an obvious rise. There are at least 500,000 newly onsets and 2 million present illness cases of AMI. SNP genetic variants were closely related to AMI. Williams et al found that a SNP in CRP (rs2592902) was closely linked to ischemic and recurrent stroke [6]. Myocardial infarction-associated SNP at 6p24 interferes with MEF2 binding and associates with PHACTR1 expression levels in human coronary arteries [7]. It is necessary to find new SNP site which was closely related to AMI

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