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Haplotype effect of the matrix metalloproteinase-1 gene on risk of myocardial infarction

Haplotype effect of the matrix metalloproteinase-1 gene on risk of myocardial infarction
Haplotype effect of the matrix metalloproteinase-1 gene on risk of myocardial infarction
Myocardial infarction (MI) is commonly caused by atherosclerotic plaque rupture following excessive degradation of collagen fibers in the atherosclerotic lesion. We investigated whether interindividual variability in risk of MI was related to polymorphisms in the gene encoding matrix metalloproteinase (MMP)-1, a key fibrillar collagen–degrading enzyme. Several single nucleotide polymorphisms in the MMP1 gene promoter were identified following sequencing DNA samples from 30 individuals. An analysis of the polymorphisms in a cohort of British whites with coronary atherosclerosis, including 639 patients with MI and 538 non-MI subjects, revealed a haplotype effect of the –519A>G and –340T>C polymorphisms on risk of MI, with the A–519-C–340 and G–519-T–340 haplotypes being protective (odds ratio=0.70 [0.57 to 0.86]; P=0.0007), whereas the G–519-C–340 haplotype increased MI risk (odds ratio=1.94 [1.15 to 3.28]; P=0.013). This finding was replicated in a subsequent analysis of 387 Swedish MI patients and 387 healthy controls (odds ratio=0.70 [0.55 to 0.89], P=0.003, for A–519-C–340 and G–519-T–340; odds ratio=1.54 [0.97 to 2.46], P=0.07, for G–519-C–340). In vitro assays showed that compared with the A–519-T–340 haplotype, the A–519-C–340 and G–519-T–340 haplotypes had lower promoter activity, whereas the G–519-C–340 haplotype had greater promoter strength, in driving gene expression in human macrophages. Haplotype-specific differences in MMP1 mRNA level in atherosclerotic tissues were also detected. The data indicate that MMP1 gene variation is a genetic factor contributing to interindividual differences in MI risk.
matrix metalloproteinase, genetics, polymorphism, haplotype analysis, atherosclerosis
0009-7330
1070-1076
Pearce, Eve
a5d03d3c-18bb-46e5-9d70-688cc5bb4c9b
Tregouet, David-Alexandre
8e9dd349-23d7-46c2-bda5-1ce42f679fb3
Samnegård, Ann
b7a1881d-530f-46b4-9711-f8e484ba23d9
Morgan, Angharad R.
f4367173-2c9b-48fd-afaf-af30867cfa8d
Cox, Charles
f2e16c89-8793-4ecc-8c82-b08e2d17a0e6
Hamsten, Anders
ff86feea-d5b9-405d-98ab-f86d05a25ad9
Eriksson, Per
b7dab14d-9f76-41c7-b1d6-f2f564454fce
Ye, Shu
132b6474-1927-4f93-80db-2c620a31c1ab
Pearce, Eve
a5d03d3c-18bb-46e5-9d70-688cc5bb4c9b
Tregouet, David-Alexandre
8e9dd349-23d7-46c2-bda5-1ce42f679fb3
Samnegård, Ann
b7a1881d-530f-46b4-9711-f8e484ba23d9
Morgan, Angharad R.
f4367173-2c9b-48fd-afaf-af30867cfa8d
Cox, Charles
f2e16c89-8793-4ecc-8c82-b08e2d17a0e6
Hamsten, Anders
ff86feea-d5b9-405d-98ab-f86d05a25ad9
Eriksson, Per
b7dab14d-9f76-41c7-b1d6-f2f564454fce
Ye, Shu
132b6474-1927-4f93-80db-2c620a31c1ab

Pearce, Eve, Tregouet, David-Alexandre, Samnegård, Ann, Morgan, Angharad R., Cox, Charles, Hamsten, Anders, Eriksson, Per and Ye, Shu (2005) Haplotype effect of the matrix metalloproteinase-1 gene on risk of myocardial infarction. Circulation Research, 97 (10), 1070-1076. (doi:10.1161/01.RES.0000189302.03303.11).

Record type: Article

Abstract

Myocardial infarction (MI) is commonly caused by atherosclerotic plaque rupture following excessive degradation of collagen fibers in the atherosclerotic lesion. We investigated whether interindividual variability in risk of MI was related to polymorphisms in the gene encoding matrix metalloproteinase (MMP)-1, a key fibrillar collagen–degrading enzyme. Several single nucleotide polymorphisms in the MMP1 gene promoter were identified following sequencing DNA samples from 30 individuals. An analysis of the polymorphisms in a cohort of British whites with coronary atherosclerosis, including 639 patients with MI and 538 non-MI subjects, revealed a haplotype effect of the –519A>G and –340T>C polymorphisms on risk of MI, with the A–519-C–340 and G–519-T–340 haplotypes being protective (odds ratio=0.70 [0.57 to 0.86]; P=0.0007), whereas the G–519-C–340 haplotype increased MI risk (odds ratio=1.94 [1.15 to 3.28]; P=0.013). This finding was replicated in a subsequent analysis of 387 Swedish MI patients and 387 healthy controls (odds ratio=0.70 [0.55 to 0.89], P=0.003, for A–519-C–340 and G–519-T–340; odds ratio=1.54 [0.97 to 2.46], P=0.07, for G–519-C–340). In vitro assays showed that compared with the A–519-T–340 haplotype, the A–519-C–340 and G–519-T–340 haplotypes had lower promoter activity, whereas the G–519-C–340 haplotype had greater promoter strength, in driving gene expression in human macrophages. Haplotype-specific differences in MMP1 mRNA level in atherosclerotic tissues were also detected. The data indicate that MMP1 gene variation is a genetic factor contributing to interindividual differences in MI risk.

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Published date: 2005
Keywords: matrix metalloproteinase, genetics, polymorphism, haplotype analysis, atherosclerosis

Identifiers

Local EPrints ID: 24900
URI: http://eprints.soton.ac.uk/id/eprint/24900
ISSN: 0009-7330
PURE UUID: 01c56db6-59fe-406b-afd2-e072f30ecf84

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Date deposited: 04 Apr 2006
Last modified: 15 Mar 2024 06:59

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Contributors

Author: Eve Pearce
Author: David-Alexandre Tregouet
Author: Ann Samnegård
Author: Angharad R. Morgan
Author: Charles Cox
Author: Anders Hamsten
Author: Per Eriksson
Author: Shu Ye

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