Analysis of the Endothelial Nitric Oxide Synthase and -fibrinogen Gene Polymorphism in the Development of Acute Myocardial Infarction in Korean Men.
10.4070/kcj.1999.29.11.1219
- Author:
Won Ha LEE
;
Tae Hong HWANG
;
Jeong Euy PARK
;
Yoon Ho CHOI
;
Jin A CHOO
;
Seonwoo KIM
;
Jong Won KIM
;
Sang Chol LEE
;
Seung Woo PARK
;
Sang Hoon LEE
;
Kyung Pyo HONG
;
Jung Don SEO
;
Won Ro LEE
- Publication Type:Original Article
- Keywords:
Myocardial infarction;
Nitric oxide synthase;
DNA polymorphism;
Smoking;
Aging
- MeSH:
Aging;
Alleles;
Endothelium;
Endothelium, Vascular;
Genotype;
Humans;
Male;
Masks;
Muscle, Smooth, Vascular;
Myocardial Infarction*;
Nitric Oxide Synthase;
Nitric Oxide Synthase Type III*;
Smoke;
Smoking
- From:Korean Circulation Journal
1999;29(11):1219-1224
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND AND OBJECTIVE: The aging process affects the responsiveness and other functions of endothelium and vascular smooth muscle cells, predisposing the old vessels to the development of atherosclerotic lesions. Endothelial nitric oxide synthase (ecNOS) gene polymorphism was shown to affect the occurrence of acute myocardial infarction (AMI). We hypothesized that aging may affect the association between the ecNOS gene polymorphism and AMI. METHODS: We investigated the age-related distribution of the ecNOS gene a/b polymorphism in 121 male AMI patients and 206 age-matched healthy male controls. As a control, we also genotyped b-fibrinogen gene H1/H2 polymorphism in the same population. RESULTS: The aa, ab, and bb genotypes were found in 1, 49 and 156 cases among the control subjects and 5, 23 and 93 cases among the AMI patients, respectively. There was a significant association between the ecNOS polymorphism and AMI (p=0.045). When the correlation was analyzed by age, the significance remained only in the group below the age of 51 (p=0.009). The distribution of the b-fibrinogen gene H1/H2 alleles, however, was not found to be associated with development of AMI in both young (p=0.7400) and old (p=0.2160) population. CONCLUSION: Our results provide the first evidence that links ecNOS polymorphism to the risk of AMI in relation to age. Young persons who smoke or have ecNOS aa genotype may have an increased risk of developing AMI. The functional as well as structural changes associated with aging in the vascular endothelium may mask the effect of the ecNOS polymorphism in the development of AMI in old people.
