Lack of association between insertion/deletion polymorphism of the angiotensin-converting enzyme gene and end-stage heart failure due to ischemic or idiopathic dilate cardiomyopathy in the Chinese

Am J Cardiol. 1996 May 1;77(11):1008-10. doi: 10.1016/s0002-9149(97)89160-6.

Abstract

Homozygosity for the deletion allele of the angiotensin-converting enzyme gene (DD) has been associated with a variety of cardiovascular diseases, including ischemic and idiopathic dilated cardiomyopathy, in Caucasians. In this study of 104 Chinese patients with end-stage heart failure due to idiopathic dilated or ischemic cardiomyopathy, the DD genotype frequency was low (12% and 11%, respectively) and was not seen more often than in a control group of 183 subjects without cardiac disease (13%). Therefore, in the Chinese, the DD genotype is less common than in Caucasians and does not appear to be associated with the development of either ischemic or idiopathic dilated cardiomyopathy.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Asian People / genetics*
  • Cardiomyopathy, Dilated / ethnology
  • Cardiomyopathy, Dilated / genetics*
  • China
  • Female
  • Gene Frequency
  • Genotype
  • Heart Failure / ethnology
  • Heart Failure / etiology
  • Heart Failure / genetics
  • Humans
  • Male
  • Middle Aged
  • Myocardial Ischemia / complications
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic*
  • Sequence Deletion

Substances

  • Peptidyl-Dipeptidase A