Matrix metalloproteinase-3 and Matrix metalloproteinase-9 genetic variation in a cohort of patients with coronary artery disease - 06/01/20
Résumé |
Introduction |
Matrix metalloproteinases (MMPs) disequilibrium in atherosclerosis plaques is influenced by genetic variations. MMP-3 and MMP-9 levels may be affected by existent single nucleotide polymorphisms: the-1171 5A/6A and the - 1562C/T respectively existent at their promoter site.
Purpose |
We aim in our study to prospectively investigate the impact of these polymorphisms on a cohort of patients with a history of coronary artery disease (CAD)
Material and Methods |
One hundred sixty-eight CAD patients were prospectively followed for 5 years. These patients were genotyped by PCR-RFLP for the MMP-9 -1562C/T and the MMP-3-1171 5A/6A polymorphism. Their levels were measured by ELISA in Sandwich test.
Results |
Forty-five fatal and non-fatal cardiovascular event occurred during the cohort period. Genotypes of both polymorphisms were in Hardy-Weinberg equilibrium. The MMP-3 5A/6A polymorphism was related to the disease on the contrary of the MMP-9. Patients carrying the 5A allele had a higher level of MMP-3 level and those who carried the 6A allele had lower level (P=0.04). MMP-9 circulating level was not related to the −1562C/T polymorphism. Individuals with the 6A allele presented a higher prevalence of the disease than the carriers of the 5A allele even after adjustment for probable confounding factors (age, gender, hypertension, diabetes, CRP, eGFR, and treatment) (HR=4.41, P:0.02 (95%CI: 1.16–16.69). Kaplan–Meier survival test revealed that individuals having the 6A allele had a lower survival rate than those with the 5A allele (P=0.01).
Conclusion |
The 6A allele is independently implicated in the occurrence of the fatal and non-fatal cardiovascular. Its existence is related to the lower survival rate.
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Vol 12 - N° 1
P. 10 - janvier 2020 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.