Loading…
Matrix metalloproteinase-2 and angiotensin-1 gene polymorphisms in patient who have coronary artery disease
Introduction: The rupture of atherosclerotic plaques is caused by the impact of matrix metalloproteinases (MMPs) upon the local fibrous valve and so might convert a chronic disease to a myocardial infarction, ultimately leading to instant death. Angiotensin converting enzyme (ACE) is actively engage...
Saved in:
Published in: | Pamukkale Medical Journal 2022, Vol.15 (1), p.29-36 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Introduction: The rupture of atherosclerotic plaques is caused by the impact of matrix metalloproteinases
(MMPs) upon the local fibrous valve and so might convert a chronic disease to a myocardial infarction, ultimately
leading to instant death. Angiotensin converting enzyme (ACE) is actively engaged in the pathogenesis of
ischemic heart disease. This study tries to unravel whether/how ACE and MMP-2 gene polymorphism contributes
to the occurrence of Coronary Artery Disease (CAD).
Materials and methods: A total of 300 individuals (100 healthy/200 patients) were included in the study. A PCRRFLP
method was utilized for ACE gene I/D and DNA sequencing MMP-2 (-1306 C/T) polymorphisms.
Results: The ACE-1 gene D/D, I/D and I/I genotype frequency of the CAD cohort was 50%, 29%, and 21%,
respectively whereas that of the healthy control cohort was 37%, 45% and 18%, respectively. Our findings
indicate that the groups differed significantly in relation to the ACE-1 genotypes (p=0.021). The frequencies of
ACE-1 gene allele I and D in both cohorts did not reveal a significant difference (p=0.314). In addition, the two
groups did not manifest MMP-2 (rs243865) gene polymorphism.
Conclusion: The association between MMP-2 gene polymorphism and CAD is too weak to suggest a conclusive
evidence. The I/D genotype frequency remained higher in the healthy individuals than in the CAD cohort, while
in the CAD group D/D genotype was more frequently than control group. Finally, the patients with D/D genotype
tend to bear greater risk for cardiovascular diseases. |
---|---|
ISSN: | 1309-9833 1308-0865 |
DOI: | 10.31362/patd.886194 |