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.

Abstract

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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