Korean J Med.
2000 Jan;58(1):19-27.
eNOS gene polymorphism in patients with acute coronary syndrome or variant
angina in Korean
- Affiliations
-
- 1Department of Internal Medicine, Seoul National University, College of Medicine, Korea.
- 2Heart Research Institute, Seoul National University Cardiovascular Labarotory.
- 3Clinical Research Institute, Seoul National University Hospital Seoul, Korea.
Abstract
-
BACKGROUND: Nitric oxide, also known as endothelial derived relaxing
factor(EDRF), regulates the vascular tone and inhibits the
proliferation of vascular smooth muscle cells and platelet adhesions
and endothelium-leukocyte interactions. Thus, nitric oxide may be
involved in the pathogenesis of atherosclerosis and vasospasm. We
analyzed the genotype distributions of two eNOS gene polymorphisms
in normal healthy Koreans and compared it with those in the patients
with acute coronary syndrome and variant angina.
METHODS
We analyzed the two eNOS polymorphisms (eNOS A/B polymorphism
is the variable numbers of tandem repeat in intron
4 and eNOS T/G polymorphism is a mis-sense mutation in exon 7) using
PCR and clinical characteristics of the risk factors for coronary
artery disease in 142 normal healthy Koreans and 164 patients with
acute coronary syndrome and 104 patients with variant angina.
RESULTS
The genotype distribution of A/B polymorphism of eNOS
gene, A/A, A/B, B/B was 4.9%, 21.1%, 74% in control group and 2.4%,
12.8%, 84.8% in the patients with acute coronary syndrome(p=0.02)
and 2.9%, 16.3%, 80.8% in the patients with variant angina(p=NS),
respectively. The genotype distribution of T/G polymorphism of
eNOS gene, T/T, T/G, G/G was 1.4%, 15.5%, 83.1% in control group
and 0.6%, 21.3%, 78.1% in the patients with acute coronary
syndrome(p=NS) and 0%, 18.3%,81.7% in the patients with variant angina(p=NS),
respectively. The odds ratio for acute coronary syndrome of non
B/B(A/A & A/B) to B/B was 0.489 (95% CI : 0.257-0.928). We found that age,
sex (male), diabetes mellitus, hyperlipidemia, smoking, B/B
genotype were independent risk factors for acute coronary syndrome.
But, in variant angina, smoking was the only significant independent
risk factor(odds ratio=5.934, 95% CI 2.843-12.388, p< 0.05).
CONCLUSION
The B/B genotype frequency of eNOS gene was significantly
higher in patients with acute coronary syndrome than in normal
controls. But neither A/B nor T/G polymorphism of eNOS gene was
associated with variant angina. These results suggest that eNOS gene
may play some roles in the pathogenesis of ACS rather than vasospasm.