Endothelin-1 and vasopressin plasma levels are not associated with the insertion/deletion polymorphism of the human angiotensin I-converting enzyme gene in patients with coronary artery disease

J Hum Hypertens. 2003 Feb;17(2):133-8. doi: 10.1038/sj.jhh.1001519.

Abstract

The objective was to investigate whether the renin-angiotensin (RA) system and related peptides endothelin-1 (ET-1) and vasopressin (VP) influence the development of coronary artery disease (CAD). Angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) gene polymorphism has been associated with the risk of CAD. The ACE I/D polymorphism determines ACE activity, but plasma levels of other RA system components remain unchanged. However, ET-1 and VP production could be increased by RA system-dependent stimulation, continually promoted by paracrine stimulation and sustained by neointimal growth. ET-1 and VP have not been associated with the ACE I/D polymorphism so far. The present study investigated the association of the ACE I/D polymorphism with plasma concentrations of ET-1 and VP, as well as with renin, angiotensin-II (AT-II) and ACE activity in 98 Caucasian individuals with CAD. ACE I/D polymorphism showed no association with plasma levels of VP, ET-1, AT-II or renin. These parameters were also not associated taking into consideration different patient variables, such as diabetes mellitus, hypertension or severity of CAD. Only plasma ACE activity was associated with the D allele. In conclusion, the ACE I/D polymorphism could not be related to plasma concentrations of VP, ET-1, renin or AT-II, but as previously demonstrated, it could only be related to ACE activity in patients with CAD. Differences in ACE activity between ACE I/D genotype subgroups are probably compensated within the RA system itself or within non-ACE pathways, so that plasma concentrations of the related peptides ET-1 and VP remain unaffected.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Angiotensin II / blood
  • Angiotensin II / genetics
  • Coronary Artery Disease / blood*
  • Coronary Artery Disease / genetics*
  • Endothelin-1 / blood*
  • Endothelin-1 / genetics*
  • Female
  • Gene Deletion*
  • Humans
  • Male
  • Middle Aged
  • Mutagenesis, Insertional / genetics*
  • Peptidyl-Dipeptidase A / blood*
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic / genetics*
  • Renin / blood
  • Renin / genetics
  • Vasoconstrictor Agents / blood*
  • Vasopressins / blood*

Substances

  • Endothelin-1
  • Vasoconstrictor Agents
  • Vasopressins
  • Angiotensin II
  • Peptidyl-Dipeptidase A
  • Renin