The GPIIIA PlA2 polymorphism is associated with an increased risk of cardiovascular adverse events

Gennaro Galasso1, Gaetano Santulli, Federico Piscione

  • 1Department of Clinical Medicine, Cardiovascular and Immunologic Sciences, Federico II University School of Medicine, Naples, Italy.

BMC Cardiovascular Disorders
|September 18, 2010
PubMed

Insights

The PlA2 polymorphism is linked to increased risks of cardiac death, myocardial infarction, and stroke in patients with atherosclerosis. This genetic factor independently predicts major adverse cardiac events and cerebrovascular events.

Area of Science:

  • Genetics
  • Cardiology
  • Neurology

Background:

  • The role of PlA2 polymorphism in thrombotic cardiovascular complications remains unclear.
  • Previous studies have yielded conflicting results regarding its clinical impact.

Purpose of the Study:

  • To investigate the effect of PlA2 polymorphism on outcomes in patients with atherosclerosis.
  • To determine if PlA2 allele presence is associated with thrombotic cardiovascular events.

Main Methods:

  • A study of 400 coronary artery disease patients undergoing percutaneous coronary intervention.
  • A replication study in 74 hypertensive patients with cerebrovascular events and 100 healthy controls.
  • PlA genotype determined by PCR-RFLP; major adverse cardiac events (MACE) recorded over a mean follow-up of 24 months.

Main Results:

  • PlA2 allele presence associated with higher cardiac death (13.1% vs 1.5%), myocardial infarction (10.7% vs 2.6%), and revascularization needs (34.8% vs 17.7%) in CAD patients.
  • Kaplan-Meier analysis showed worse long-term outcome for patients with PlA2 allele (p=0.015).
  • PlA2 independently predicted cardiac death (OR: 9.594) and MACE (OR: 1.829); increased stroke risk (OR: 4.1) in replication study.

Conclusions:

  • The PlA2 allele is associated with an increased risk of thrombotic cardiovascular complications in patients with severe atherosclerosis.
  • PlA2 polymorphism serves as an independent predictor for adverse cardiovascular and cerebrovascular events.
Abstract

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