ACE I/D polymorphism in different etiologies of ischemic stroke

Acta Neurol Scand. 2006 Nov;114(5):320-2. doi: 10.1111/j.1600-0404.2006.00672.x.

Abstract

Objectives: Data concerning an association between angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D) polymorphism and ischemic stroke (IS) remain inconsistent. Results of some studies suggest that DD genotype may be a risk factor for small vessel disease (SVD) stroke. Here, we investigated whether this polymorphism is associated with IS of different etiologies in a Polish population.

Subjects and methods: Ischemic stroke etiology was established according to the TOAST criteria. We studied 92 stroke patients with large vessel disease and their 184 matched controls; 96 stroke patients with SVD and 192 controls; 180 patients with cardioembolic stroke (CE) and 180 controls. ACE I/D polymorphism was determined using the polymerase chain reaction method.

Results: The distribution of ACE genotypes and alleles was essentially the same in all analyzed IS subtypes and their matched controls.

Conclusions: We failed to find an association between ACE polymorphism and etiological subtypes of IS in a Polish population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Brain Ischemia / enzymology*
  • Brain Ischemia / genetics*
  • Brain Ischemia / physiopathology
  • DNA Mutational Analysis
  • Female
  • Gene Deletion
  • Gene Frequency
  • Genetic Markers / genetics
  • Genetic Predisposition to Disease / genetics
  • Genetic Testing
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Mutation / genetics
  • Peptidyl-Dipeptidase A / genetics*
  • Poland
  • Polymorphism, Genetic / genetics*
  • Stroke / enzymology*
  • Stroke / genetics*
  • Stroke / physiopathology

Substances

  • Genetic Markers
  • Peptidyl-Dipeptidase A