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Matrix Metalloproteinase 3 Gene Polymorphism and Its Level Predict Morbidity After Acute Myocardial Infarction
Tarek A Abd El-Aziz1, Randa H Mohamed2
1From the Cardiology Department.
Objectives:
Matrix metalloproteinase is responsible for ventricular remodeling after acute myocardial infarction (MI). The purpose of the present study was to determine whether the matrix metalloproteinase 3 (MMP-3) polymorphism and its level predict morbidity after acute MI (AMI).
Methods:
We studied 112 patients with AMI and 140 controls. All patients were followed for AMI complications during their hospitalization and 6 months after. Serum MMP-3 was measured. MMP-3-1612 5A/6A polymorphism was genotyped by polymerase chain reaction.
Results:
We observed that the serum MMP-3 levels were significantly increased in patients with AMI with morbidity compared with patients without complications. Also, MMP-3 levels in patients with AMI carrying 5A/5A were elevated compared with those carrying 6A/6A. The frequencies of 5A/5A genotypes were significantly increased in patients with AMI compared with controls, and patients with AMI carrying 5A/5A had a fivefold increased risk of developing morbidity. The impairment of left ventricular function (ΔFS [fractional shortening] and ΔEF [ejection fraction]) was observed more in the 5A/5A genotype compared with the 6A/6A genotype. A significant inverse correlation between predischarge MMP-3 levels and FS and EF was found at 6 months follow-up.
Conclusions:
MMP-3 polymorphism has a significant association with the risk of developing morbidity after AMI. Higher predischarge MMP-3 levels are associated with left ventricular dysfunction after AMI.
Insights
Matrix metalloproteinase 3 (MMP-3) gene variants and elevated MMP-3 levels predict complications after acute myocardial infarction (AMI). The 5A/5A genotype is linked to increased morbidity and impaired left ventricular function post-MI.
Area of Science:
- Cardiology
- Genetics
- Biochemistry
Background:
- Matrix metalloproteinases (MMPs) play a crucial role in ventricular remodeling following acute myocardial infarction (MI).
- Matrix metalloproteinase 3 (MMP-3) is implicated in post-MI cardiac remodeling.
- Genetic variations in MMP genes may influence patient outcomes after MI.
Purpose of the Study:
- To investigate the association between MMP-3 gene polymorphism (5A/6A) and serum MMP-3 levels with morbidity after acute myocardial infarction (AMI).
- To determine if MMP-3 status predicts adverse outcomes and left ventricular dysfunction in AMI patients.
Main Methods:
- A cohort of 112 patients with AMI and 140 controls were studied.
- Serum MMP-3 levels were measured, and MMP-3-1612 5A/6A polymorphism was genotyped using polymerase chain reaction.
- Patients were followed for AMI complications during hospitalization and for 6 months post-discharge.
Main Results:
- Serum MMP-3 levels were significantly higher in AMI patients who experienced morbidity compared to those without complications.
- Patients with the MMP-3 5A/5A genotype exhibited elevated MMP-3 levels and a fivefold increased risk of morbidity.
- The 5A/5A genotype was associated with greater impairment in left ventricular fractional shortening and ejection fraction, and higher MMP-3 levels correlated inversely with these parameters at 6 months.
Conclusions:
- MMP-3 gene polymorphism, specifically the 5A/5A genotype, is significantly associated with an increased risk of morbidity after AMI.
- Elevated predischarge serum MMP-3 levels are linked to the development of left ventricular dysfunction in the aftermath of an acute myocardial infarction.
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