The deletion allele of the angiotensin I converting enzyme gene as a genetic susceptibility factor for cognitive impairment

Neurosci Lett. 1996 Oct 18;217(2-3):203-5.

Abstract

Experimental evidences suggest an implication of the renin angiotensin system (RAS) as a potential determinant of cognitive functions. To explore this hypothesis, we compared the distribution of an insertion (I)/deletion (D) polymorphism of the gene coding for the angiotensin I converting enzyme (ACE), a key enzyme of the RAS, in 228 elderly with cognitive impairment to that of 255 controls. The ACE D allele frequency was higher in the group with cognitive impairment (0.594) than in controls (0.514) (P < 0.02). The ACE DD genotype carriers had an increased risk of cognitive impairment (OR = 1.60, 95% CI (1.04-2.36), P < 0.03), independent of other risk factors of cognitive impairment: age, gender and presence of the apolipoprotein E epsilon 4 allele. This association was stronger in men (OR = 3.25, 95% CI (1.40-7.58), P < 0.006). This result suggests a possible implication of the RAS in human brain and cognitive functions.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles*
  • Apolipoproteins E / genetics
  • Cognition Disorders / epidemiology*
  • Cognition Disorders / genetics*
  • DNA / analysis
  • DNA / blood
  • Female
  • France / epidemiology
  • Gene Deletion*
  • Gene Frequency*
  • Genotype
  • Humans
  • MMPI
  • Male
  • Middle Aged
  • Odds Ratio
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic
  • Risk Factors

Substances

  • Apolipoproteins E
  • DNA
  • Peptidyl-Dipeptidase A