Interaction of angiotensin-converting enzyme and apolipoprotein E gene polymorphisms in ischemic stroke involving large-vessel disease

J Thromb Thrombolysis. 2009 Jan;27(1):68-74. doi: 10.1007/s11239-007-0165-y. Epub 2007 Nov 21.

Abstract

A relationship between apolipoprotein E (Apo E) genotype and angiotensin-converting enzyme (ACE) insertion-deletion (Ins-Del) mutation and stroke was suggested. We investigated the association of Apo E4 and ACE Ins/Del genotypes with stroke risk and changes in serum lipids in 228 consecutive Tunisian stroke patients, and 323 age-and gender-matched controls. Comparable frequencies of ACE Ins/Del alleles were seen between patients and controls. The prevalence of Apo epsilon3 allele and Apo E3/E3 were lower (P < 0.001), while the frequency of Apo epsilon4 allele and epsilon4-containing genotypes (E3/E4 and E4/E4) were elevated (P < 0.001) among patients. Higher proportion of Apo E4-carrying + ACE Del/Del positive cases were seen in young (<50 years) patients (P = 0.012), and was associated with large vessel stroke (P = 0.035). Mean serum cholesterol, LDL, HDL, and triglycerides were comparable between E4-containing and no E4-containing and ACE Del/Del-positive patients. Apo E4 and ACE Del/Del genotype combination substantially increase stroke risk, supporting the notion that interactions of multiple gene variants influence stroke pathogenesis.

MeSH terms

  • Age Factors
  • Aged
  • Alleles
  • Apolipoprotein E3 / genetics*
  • Apolipoprotein E4 / genetics*
  • Brain Ischemia / epidemiology
  • Brain Ischemia / etiology
  • Brain Ischemia / genetics*
  • Case-Control Studies
  • Comorbidity
  • Epigenesis, Genetic*
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Intracranial Arteriosclerosis / complications
  • Intracranial Arteriosclerosis / epidemiology
  • Intracranial Arteriosclerosis / genetics*
  • Lipids / blood
  • Male
  • Middle Aged
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Risk Factors
  • Sequence Deletion
  • Tunisia / epidemiology

Substances

  • Apolipoprotein E3
  • Apolipoprotein E4
  • Lipids
  • Peptidyl-Dipeptidase A