Common intronic D variant of ACE gene is associated with endothelial dysfunction in COPD

Respir Med. 2013 Aug;107(8):1217-21. doi: 10.1016/j.rmed.2012.12.025. Epub 2013 May 20.

Abstract

Background: Pathogenesis of chronic obstructive lung disease (COPD) includes primary inflammatory events, multiple vascular reactions, remodeling of bronchial and vascular walls.

Objective: The aim of present single-center study was to assess relations between angiotensin-converting enzyme (ACE) gene and prevalence of clinical symptoms characteristic to COPD.

Methods: The study involved sixty-three male patients with COPD (44-86 years old, a mean of 60.4 years). COPD diagnostics was performed according to common criteria, including evaluation of systolic pressure in pulmonary artery (SPPA) and endothelial disfunction (ED). Genotyping of ACE I/D was performed by means of gene-specific PCR.

Results: 1. Allele distribution of studied gene alleles among COPD patients did not differ from control age-matched group. 2. Detectable endothelial dysfunction in COPD patients was shown to correlate with high-producer D allele of ACE gene, at an odds ratio of 6.632 (CI = 1.67-26.31; chi2 = 8.39, p = 0.004). Moreover, detectable ED correlated with numbers of COPD exacerbations per year.

Conclusions: These findings suggest possible association of the functional ACE D allele with altered vascular responses that may modulate development of distinct COPD symptoms. The results are obtained in a limited clinical cohort, and deserve repeated trials in other groups of COPD patients.

Keywords: Angiotensin-converting enzyme; Chronic obstructive lung disease; Endothelial dysfunction; Gene polymorphism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Ankle Brachial Index
  • Arterial Pressure / physiology
  • Case-Control Studies
  • Dilatation, Pathologic / genetics
  • Dilatation, Pathologic / physiopathology
  • Endothelium, Vascular / physiopathology*
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Peptidyl-Dipeptidase A / genetics*
  • Polymorphism, Genetic / genetics*
  • Pulmonary Artery / physiology
  • Pulmonary Disease, Chronic Obstructive / genetics*
  • Pulmonary Disease, Chronic Obstructive / physiopathology
  • Vascular Diseases / genetics*
  • Vascular Diseases / physiopathology

Substances

  • Peptidyl-Dipeptidase A