High CA repeat numbers in intron 13 of the endothelial nitric oxide synthase gene and increased risk of coronary artery disease

被引:53
作者
Stangl, K
Cascorbi, I
Laule, M
Klein, T
Stangl, V
Rost, S
Wernecke, KD
Felix, SB
Bindereif, A
Baumann, G
Roots, I
机构
[1] Humboldt Univ, Med Klin, Schwerpunkt Kardiol Angiol & Pneumol, D-10098 Berlin, Germany
[2] Humboldt Univ, Inst Klin Pharmakol, D-10098 Berlin, Germany
[3] Humboldt Univ, Inst Med Biometrie, D-10098 Berlin, Germany
[4] Humboldt Univ, Inst Biochem, D-10098 Berlin, Germany
来源
PHARMACOGENETICS | 2000年 / 10卷 / 02期
关键词
coronary artery disease; CA repeat; endothelial nitric oxide synthase; polymorphism;
D O I
10.1097/00008571-200003000-00005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Endothelial nitric oxide synthase (eNOS) plays a key role in vascular homeostasis. Because its product, nitric oxide, possesses vasodilatory and antiatherogenic properties, an altered eNOS function might promote atherosclerosis, We investigated the association between variations in CA repeat copy number [(CA), polymorphism] in intron 13 of the eNOS gene and the risk of coronary artery disease, (CA), polymorphism was investigated in 1000 consecutive patients with angiographically confirmed coronary artery disease and 1000 age- and gender-matched control subjects by a PCR-based fragment length calculation, Twenty-eight different alleles were identified containing 17-44 CA repeats. The presence of one allele containing greater than or equal to 38 repeats was associated with an excess risk of coronary artery disease (odds ratio 1.94, 95% confidence interval 1.31-2.86, P = 0.001). Carriers of alleles containing greater than or equal to 38 CA repeats were, in particular, overrepresented in the subgroup without common cardiovascular risk factors (odds ratio 3.39, 95% confidence interval 1.30-8.86, P = 0.009). Logistic regression analysis revealed that the (CA), polymorphism proved to be an independent risk factor (relative risk 2.17, 95% confidence interval 1.44-3.27, P = 0.0002). Our findings indicate that high numbers of CA repeats in intron 13 of the eNOS gene are associated with an excess risk of coronary artery disease, Pharmacogenetics 10:133-140 (C) 2000 Lippincott Williams & Wilkins.
引用
收藏
页码:133 / 140
页数:8
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