Genetic Polymorphism of Matrix Metalloproteinase-9 and Susceptibility to Myocardial Infarction: A Meta-Analysis

被引:9
作者
Feng, Beili [1 ,2 ]
Li, Hengdong [1 ,2 ]
机构
[1] Univ Chinese Acad Sci, HwaMei Hosp, Dept Cardiol, Ningbo, Zhejiang, Peoples R China
[2] Univ Chinese Acad Sci, Ningbo Inst Life & Hlth Ind, Ningbo, Zhejiang, Peoples R China
关键词
CORONARY-ARTERY-DISEASE; MATRIX METALLOPROTEINASES; ATHEROSCLEROSIS; ASSOCIATION; HEART; MMP-9;
D O I
10.1155/2022/5507153
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
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页数:8
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共 29 条
[1]   Matrix metalloproteinase-9 polymorphism and outcome after acute myocardial infarction [J].
Abd El-Aziz, Tarek A. ;
Mohamed, Rasha H. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2017, 227 :524-528
[2]  
[Anonymous], 2007, J CLIN HEMATOLOGY
[3]   The TIMI risk score for unstable angina/non-ST elevation MI - A method for prognostication and therapeutic decision making [J].
Antman, EM ;
Cohen, M ;
Bernink, PJLM ;
McCabe, CH ;
Horacek, T ;
Papuchis, G ;
Mautner, B ;
Corbalan, R ;
Radley, D ;
Braunwald, E .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 284 (07) :835-842
[4]   Myocardial Infarction-Associated SNP at 6p24 Interferes With MEF2 Binding and Associates With PHACTR1 Expression Levels in Human Coronary Arteries [J].
Beaudoin, Melissa ;
Gupta, Rajat M. ;
Won, Hong-Hee ;
Lo, Ken Sin ;
Do, Ron ;
Henderson, Christopher A. ;
Lavoie-St-Amour, Claire ;
Langlois, Simon ;
Rivas, Daniel ;
Lehoux, Stephanie ;
Kathiresan, Sekar ;
Tardif, Jean-Claude ;
Musunuru, Kiran ;
Lettre, Guillaume .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2015, 35 (06) :1472-1479
[5]   Acute myocardial infarction [J].
Boateng, Stephen ;
Sanborn, Timothy .
DM DISEASE-A-MONTH, 2013, 59 (03) :83-96
[6]   Timeline - Matrix metalloproteinases: a tail of a frog that became a prince [J].
Brinckerhoff, CE ;
Matrisian, LM .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (03) :207-214
[7]   IDENTIFICATION OF 92-KD GELATINASE IN HUMAN CORONARY ATHEROSCLEROTIC LESIONS - ASSOCIATION OF ACTIVE ENZYME-SYNTHESIS WITH UNSTABLE ANGINA [J].
BROWN, DL ;
HIBBS, MS ;
KEARNEY, M ;
LOUSHIN, C ;
ISNER, JM .
CIRCULATION, 1995, 91 (08) :2125-2131
[8]  
[陈晓锋 Chen Xiaofeng], 2005, [中国动脉硬化杂志, Chinese Journal of Arteriosclerosis], V13, P775
[9]   Acute actions and novel targets of matrix metalloproteinases in the heart and vasculature [J].
Chow, A. K. ;
Cena, J. ;
Schulz, R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2007, 152 (02) :189-205
[10]   Influences of IL-1b-3953 C&gt;T and MMP-9-1562C&gt;T Gene Variants on Myocardial Infarction Susceptibility in a Subset of the Iranian Population [J].
Daraei, Abdolreza ;
Mansoori, Yaser ;
Zendebad, Zahra ;
Tavakkoly-Bazzaz, Javad ;
Madadizadeh, Farzan ;
Naghizadeh, Mohammad Mehdi ;
Arghavani, Ali ;
Mansoori, Behnam .
GENETIC TESTING AND MOLECULAR BIOMARKERS, 2017, 21 (01) :33-38