Lack of an association between angiotensin-converting enzyme gene insertion/deletion polymorphism and ischaemic stroke

Eur Neurol. 2004;51(3):148-52. doi: 10.1159/000077203. Epub 2004 Mar 8.

Abstract

Background and purpose: Numerous factors have been reported to influence the pathogenesis of stroke. The angiotensin I-converting enzyme (ACE) gene is a candidate gene for atherosclerotic-related diseases. In the present study, the association between the polymorphism of the ACE gene and ischaemic stroke was investigated.

Methods: Using polymerase chain reaction techniques, 100 patients (48 males, age 69.3 +/- 9.7 years) with cerebral infarction and 100 age- and sex-matched controls were divided into the following three ACE genotypes [deletion (D) and insertion (I)]: II, ID and DD.

Results: There was no evidence of any association between the ACE gene polymorphism and the presence of ischaemic stroke (odds ratio 0.874, 95% confidence interval 0.386-1.973).

Conclusions: The DD genotype in the human ACE gene does not appear to be a risk factor for ischaemic stroke. Further evaluation in a larger population study is required to examine the possibility of an increased risk of ischaemic stroke in DD homozygotes.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Brain Ischemia / genetics*
  • Case-Control Studies
  • DNA Mutational Analysis / methods
  • Female
  • Gene Deletion*
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Mutagenesis, Insertional*
  • Peptidyl-Dipeptidase A / genetics*
  • Polymerase Chain Reaction / methods
  • Polymorphism, Genetic*

Substances

  • Peptidyl-Dipeptidase A