Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease
Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease
Matrix metalloproteinase-9 (MMP-9) plays an important role in the pathogenesis of atherosclerosis, the pathology underlying the majority of coronary artery disease. We previously identified several polymorphisms in the gene encoding MMP-9. In this study we tested the hypothesis that variation in the matrix metalloproteinase-9 gene influences the development of atherosclerosis. Three common polymorphisms, i.e. m1562C>T, R+279Q and +6C>T, were analysed in 1510 white subjects undergoing coronary angiography. Analyses of individual polymorphisms showed that the frequencies of the C/T and T/T genotypes of the m1562C>T polymorphism were significantly higher in patients with coronary stenosis than in those with a normal angiogram. Logistic regression analyses indicated that individuals carrying the m1562T allele had an approx. 1.5-fold higher risk of developing coronary stenosis (OR 1.49, 95% CI 1.039-2.144), which was equivalent to an over 30% reduction in risk of coronary stenosis in individuals not carrying this allele (OR 0.670, 95% CI 0.467-0.963). The three polymorphisms studied were found to be in strong linkage disequilibrium. Haplotype analyses showed that the C-G-C haplotype (m1562C, +279Q and +6C) was associated with a protective effect against atherosclerosis. Individuals carrying this haplotype were at reduced risk of developing coronary stenosis (OR 0.695, 95% CI 0.530.92). Furthermore, the C-G-C haplotype was associated with less severe coronary atherosclerosis, i.e. carriers of this haplotype were at a lower risk of having coronary stenosis in more than one coronary artery (OR 0.796, 95% CI 0.640.99). These data, together with the previous finding that the m1562T allele has a higher transcriptional activity than the m1562C allele, support the notion that genetic variation with an effect on MMP-9 expression influences the development and progression of atherosclerosis.
matrix metalloproteinase, genetic polymorphism, haplotype, coronary artery disease
321-326
Morgan, Angharad R.
f4367173-2c9b-48fd-afaf-af30867cfa8d
Zhang, Baiping
94e2efcc-d26f-41df-9069-9be5db88a5a1
Tapper, William
9d5ddc92-a8dd-4c78-ac67-c5867b62724c
Collins, Andrew
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Ye, Shu
132b6474-1927-4f93-80db-2c620a31c1ab
2003
Morgan, Angharad R.
f4367173-2c9b-48fd-afaf-af30867cfa8d
Zhang, Baiping
94e2efcc-d26f-41df-9069-9be5db88a5a1
Tapper, William
9d5ddc92-a8dd-4c78-ac67-c5867b62724c
Collins, Andrew
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Ye, Shu
132b6474-1927-4f93-80db-2c620a31c1ab
Morgan, Angharad R., Zhang, Baiping, Tapper, William, Collins, Andrew and Ye, Shu
(2003)
Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease.
Journal of Molecular Medicine, 81 (5), .
(doi:10.1007/s00109-003-0441-z).
Abstract
Matrix metalloproteinase-9 (MMP-9) plays an important role in the pathogenesis of atherosclerosis, the pathology underlying the majority of coronary artery disease. We previously identified several polymorphisms in the gene encoding MMP-9. In this study we tested the hypothesis that variation in the matrix metalloproteinase-9 gene influences the development of atherosclerosis. Three common polymorphisms, i.e. m1562C>T, R+279Q and +6C>T, were analysed in 1510 white subjects undergoing coronary angiography. Analyses of individual polymorphisms showed that the frequencies of the C/T and T/T genotypes of the m1562C>T polymorphism were significantly higher in patients with coronary stenosis than in those with a normal angiogram. Logistic regression analyses indicated that individuals carrying the m1562T allele had an approx. 1.5-fold higher risk of developing coronary stenosis (OR 1.49, 95% CI 1.039-2.144), which was equivalent to an over 30% reduction in risk of coronary stenosis in individuals not carrying this allele (OR 0.670, 95% CI 0.467-0.963). The three polymorphisms studied were found to be in strong linkage disequilibrium. Haplotype analyses showed that the C-G-C haplotype (m1562C, +279Q and +6C) was associated with a protective effect against atherosclerosis. Individuals carrying this haplotype were at reduced risk of developing coronary stenosis (OR 0.695, 95% CI 0.530.92). Furthermore, the C-G-C haplotype was associated with less severe coronary atherosclerosis, i.e. carriers of this haplotype were at a lower risk of having coronary stenosis in more than one coronary artery (OR 0.796, 95% CI 0.640.99). These data, together with the previous finding that the m1562T allele has a higher transcriptional activity than the m1562C allele, support the notion that genetic variation with an effect on MMP-9 expression influences the development and progression of atherosclerosis.
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Published date: 2003
Keywords:
matrix metalloproteinase, genetic polymorphism, haplotype, coronary artery disease
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Local EPrints ID: 24869
URI: http://eprints.soton.ac.uk/id/eprint/24869
ISSN: 0946-2716
PURE UUID: 79033135-9c30-4b23-a386-7e88d4e6d417
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Date deposited: 04 Apr 2006
Last modified: 16 Mar 2024 03:07
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Author:
Angharad R. Morgan
Author:
Baiping Zhang
Author:
Shu Ye
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