Kim In Jai, Bae Jeehyeon, Lim Sang Wook, Cha Dong Hoon, Cho Hyo Jin, Kim Sun, Yang Dong Ho, Hwang Seong Gyu, Oh Doyeun, Kim Nam Keun
Institute for Clinical Research, Bundang CHA General Hospital, College of Medicine, Pochon CHA University, 351 Yatap-Dong, Bundang-Gu, Seongnam, South Korea.
Thromb Res. 2007;119(5):579-85. doi: 10.1016/j.thromres.2006.06.005. Epub 2006 Jul 13.
Endothelium-derived nitric oxide (NO) is synthesized from l-arginine by endothelial nitric oxide synthase (eNOS) encoded by the eNOS3 gene on chromosome 7. The effects of the eNOS polymorphisms with the risk of coronary artery disease are conflicting. In this study, we investigated the association of the eNOS genotypes with coronary artery disease in Koreans.
A case-control study was performed to evaluate the association between the eNOS -786T>C, 4a4b, or 894G>T polymorphism and coronary artery disease. 147 consecutive patients with coronary artery disease and 222 healthy controls were recruited. The genotypes of eNOS -786T>C and 894G>T polymorphisms were determined by the polymerase chain reaction-restriction fragment length polymorphism analysis. The genotypes of a 27 bp insertion/deletion in intron 4 (eNOS 4a4b) were determined by the banding pattern on gel electrophoresis.
The eNOS -786T>C (odds ratio [OR]; 1.61, 95% confidence interval [CI]; 0.97-2.69), 894G>T (OR; 1.12, 95% CI; 0.65-1.92) and 4a4b (OR; 1.44, 95% CI; 0.87-2.39) polymorphisms were not an independent predisposition factor to coronary artery disease. However, a subgroup analysis adjusted with various cardiovascular risk factors confirmed positive association of the -786T>C polymorphism in CAD patients with hypertension and a smoking history and also a significant association of the intron 4 genotypes with a smoking history, but no significance has been found in the eNOS polymorphisms of 894G>T upon any risk adjustment. In this study we also found that the distribution of heterozygotes (-786TC, 894GT, and 4a4b) and variant homozygotes for the -786C, 894T, and intron 4a alleles of eNOS in Koreans were significantly lower than in Caucasian populations.
The present study demonstrates that polymorphisms of the eNOS -786T>C and 4a4b are associated with coronary artery disease with adjustments for cardiovascular risk factors in the Koreans.
内皮源性一氧化氮(NO)由7号染色体上eNOS3基因编码的内皮型一氧化氮合酶(eNOS)从L-精氨酸合成。eNOS基因多态性与冠状动脉疾病风险之间的关系存在争议。在本研究中,我们调查了韩国人中eNOS基因分型与冠状动脉疾病的关联。
进行了一项病例对照研究,以评估eNOS -786T>C、4a4b或894G>T基因多态性与冠状动脉疾病之间的关联。招募了147例连续的冠状动脉疾病患者和222例健康对照。通过聚合酶链反应-限制性片段长度多态性分析确定eNOS -786T>C和894G>T基因多态性的基因型。通过凝胶电泳上的条带模式确定内含子4中27 bp插入/缺失(eNOS 4a4b)的基因型。
eNOS -786T>C(优势比[OR];1.61,95%置信区间[CI];0.97 - 2.69)、894G>T(OR;1.12,95% CI;0.65 - 1.92)和4a4b(OR;1.44,95% CI;0.87 - 2.39)基因多态性不是冠状动脉疾病的独立易患因素。然而,一项根据各种心血管危险因素进行调整的亚组分析证实,CAD患者中-786T>C基因多态性与高血压和吸烟史呈正相关,内含子4基因型与吸烟史也有显著关联,但在任何风险调整后,894G>T的eNOS基因多态性均无显著性。在本研究中,我们还发现韩国人中eNOS的-786C、894T和内含子4a等位基因的杂合子(-786TC、894GT和4a4b)和变异纯合子的分布显著低于白种人群。
本研究表明,在韩国人中,对心血管危险因素进行调整后,eNOS -786T>C和4a4b基因多态性与冠状动脉疾病相关。