Clinical restenosis after coronary stent implantation is associated with the heme oxygenase-1 gene promoter polymorphism and the heme oxygenase-1 +99G/C variant.

Abstract

BACKGROUND:

Vascular remodeling after percutaneous coronary stent implantation frequently leads to restenosis. Heme oxygenase 1 (HO-1) is involved in the generation of the endogenous antioxidant bilirubin and carbon monoxide, both of which exert antiinflammatory and antiproliferative effects. The aim of the present study was to evaluate the influence of genetic risk factors combined with the conventional risk factors on the development of coronary restenosis after percutaneous coronary intervention (PCI) with stent implantation.

METHODS:

The HO-1 gene GT dinucleotide repeat promoter polymorphism and HO-1 +99G/C variant were evaluated in 199 patients with coronary artery disease after coronary stent implantation and control angiography at 6 months after the intervention. Coronary restenosis was confirmed by quantitative angiography.

RESULTS:

Carriers of the long allele of the HO-1 gene promoter (>29 repeats) had a significantly higher risk of developing restenosis after PCI than noncarriers [odds ratio (OR)=1.9; 95% confidence interval (95% CI), 1.0-3.4; P=0.04]. Interestingly, the allele longer than 29 repeats conferred a significantly higher risk of developing restenosis (OR=3.4; 95% CI, 1.2-9.1; P=0.017) in nonsmokers than in smokers (OR=2.0; 95% CI, 0.7-5.2; P=0.18).

CONCLUSIONS:

The long allele of the HO-1 gene promoter (>29 repeats) polymorphism, which leads to low HO-1 inducibility, may represent an independent prognostic marker for restenosis after PCI and stent implantation. The effect of the >29 repeat allele is attenuated in smokers, who have chronic exogenous CO exposure.

• Authors: Talin Gulesserian, Catharina Wenzel, Georg Endler, Raute Sunder-Plassmann, Claudia Marsik, Christine Mannhalter, Nelly Iordanova, Mariann Gyöngyösi, Johann Wojta, Stefan Mustafa, Oswald Wagner, Kurt Huber
• Journal: Clinical chemistry (Clin Chem) Vol. 51 Issue 9 Pg. 1661-5 (Sep 2005) ISSN: 0009-9147 [Print] England
• PMID: 16020495 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Isoenzymes
• Membrane Proteins
• HMOX1 protein, human
• Heme Oxygenase (Decyclizing)
• Heme Oxygenase-1

Topics

• Aged
• Amino Acid Substitution
• Angioplasty, Balloon, Coronary (adverse effects)
• Coronary Restenosis (etiology, genetics)
• Cross-Sectional Studies
• Female
• Genotype
• Heme Oxygenase (Decyclizing) (genetics)
• Heme Oxygenase-1
• Humans
• Isoenzymes (genetics)
• Male
• Membrane Proteins
• Middle Aged
• Polymorphism, Genetic
• Promoter Regions, Genetic
• Risk Assessment
• Smoking (adverse effects)
• Stents (adverse effects)