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Scholars Journal of Applied Medical Sciences | Volume-4 | Issue-07
Association of Matrix Metalloproteinase-2 Gene Promoter Polymorphism and the Associated Phenotype Variation with Myocardial Infarction
Dr. B. Sudhapresanna, Dr. V. Ananthan, Dr. S. Sumathy, Dr. S. Siva, Dr. Pragna B. Dolia, Dr. C. Shanmuga Priya
Published: July 30, 2016 | 63 67
DOI: 10.36347/sjams.2016.v04i07.024
Pages: 2417-2422
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Abstract
MatrixMetalloProteinases-2, are zinc dependent endopeptidases which degrade major components of the basal lamina around blood vessels. Myocardial Infarction is mainly due to atherosclerosis of the coronary arteries. MMP-2 destabilizes the arterial wall and breaks atheromatous plaque leading to MI. The gene for human MMP-2 contains 27,862 base pair genomic DNA and is composed of 13 exons. Several common restriction fragment length polymorphisms (RFLPs) have been reported in the MMP-2 gene locus. 100 diagnosed myocardial infarction patients were taken as cases. 100 Age, sex matched individuals taken as controls. Autoimmune, thyroid, neoplastic, hepatic and chronic infections were excluded. Plasma MMP-2 levels were determined by ELISA and Genotyping was done by PCR-RFLP. Plasma MMP-2 level was increased in patients with myocardial infarction. Genotype frequency distribution between cases and controls were compared with a 2 test. MMP-2 activity was compared between controls and cases by Student t test, p value < 0.05 was considered significant.