Heme oxygenase-1 microsatellite polymorphism and haplotypes are associated with the development of acute respiratory distress syndrome

Intensive Care Med. 2009 Aug;35(8):1343-51. doi: 10.1007/s00134-009-1504-6. Epub 2009 Jun 13.

Abstract

Objective: Heme oxygenase-1 (HO-1) acts in cytoprotection against acute lung injury. The polymorphic (GT)n repeat in the HO-1 gene (HMOX1) promoter regulates HMOX1 expression. We investigated the associations of HMOX1 polymorphisms with acute respiratory distress syndrome (ARDS) risk and plasma HO-1 levels.

Design: Unmatched, nested case-control study.

Setting: Academic medical center.

Patients: Consecutive patients with ARDS risk factors upon ICU admission were prospectively enrolled. Cases were 437 Caucasians who developed ARDS and controls were 1,014 Caucasians who did not.

Measurements and results: We genotyped the (GT)n polymorphism and three tagging single nucleotide polymorphisms (tSNPs) in 1,451 patients, and measured the plasma HO-1 levels in 106 ARDS patients. We clustered the (GT)n repeats into: S-allele (<24 repeats), M-allele (24-30 repeats) and L-allele (> or = 31 repeats). We found that longer (GT)n repeats were associated with reduced ARDS risk (Ptrend = 0.004 for both alleles and genotypes), but no individual tSNP was associated with ARDS risk. HMOX1 haplotypes were significantly associated with ARDS risk (global test, P = 0.016), and the haplotype S-TAG was associated with increased ARDS risk (OR, 1.75; 95% CI, 1.15-2.68; P = 0.010). Intermediate-phenotype analysis showed longer (GT)n repeats were associated with higher plasma HO-1 levels (Ptrend = 0.019 for alleles and 0.027 for genotypes).

Conclusions: Longer (GT)n repeats in the HMOX1 promoter are associated with higher plasma HO-1 levels and reduced ARDS risk. The common haplotype S-TAG is associated with increased ARDS risk. Our results suggest that HMOX1 variation may modulate ARDS risk through the promoter microsatellite polymorphism.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Aged, 80 and over
  • Case-Control Studies
  • Critical Care
  • Female
  • Genetic Predisposition to Disease
  • Haplotypes*
  • Heme Oxygenase-1 / blood
  • Heme Oxygenase-1 / genetics*
  • Humans
  • Male
  • Microsatellite Repeats*
  • Middle Aged
  • Molecular Epidemiology
  • Polymorphism, Genetic / physiology*
  • Respiratory Distress Syndrome / genetics*
  • Respiratory Distress Syndrome / physiopathology
  • Risk Factors

Substances

  • HMOX1 protein, human
  • Heme Oxygenase-1