Lack of association of angiotensin-converting enzyme insertion/deletion polymorphism and myocardial infarction at very young ages

Biomarkers. 2009 Sep;14(6):401-5. doi: 10.1080/13547500903039966.

Abstract

We examined whether angiotensin-converting enzyme (ACE) insertion (I)/deletion (D) polymorphism is associated with the development of myocardial infarction (MI) at < or = 35 years of age. The study sample consisted of 201 patients with premature MI and 140 age- and sex-matched healthy individuals. No difference was found in the distribution of ACE genotypes between the patients and controls. A higher prevalence of the DD genotype among hypertensives was found compared with the non-hypertensive patients (62.5% vs 35.6%, p = 0.01). ACE polymorphism is not associated with the development of premature MI and this might be due to the low prevalence of hypertension in young coronary patients.

MeSH terms

  • Adult
  • Age of Onset
  • Case-Control Studies
  • Female
  • Genotype
  • Humans
  • Hypertension
  • Male
  • Myocardial Infarction / etiology
  • Myocardial Infarction / genetics*
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Sequence Deletion

Substances

  • Peptidyl-Dipeptidase A