Yahashi Y, Kario K, Shimada K, Matsuo M
Division of Genetics, International Center for Medical Research, Kobe University School of Medicine, Japan.
Blood Coagul Fibrinolysis. 1998 Jul;9(5):405-9. doi: 10.1097/00001721-199807000-00002.
Endothelium-derived nitric oxide formed by endothelial constitutive nitric oxide synthase (ecNOS) mediates endothelium-dependent vasodilation and antithrombotic action. We analyzed the distribution of a polymorphism of ecNOS (27-bp repeat in intron 4) in 127 ischemic stroke patients (18 with atherothrombotic, 58 with lacunar, and 51 with silent lacunar stroke) and 91 control subjects. When we assigned the four repeats as allele a, and five repeats as allele b, there was no significant difference between the genotype distribution and allele frequencies in the stroke group and in the control group (0.862 versus 0.868 for the b allele frequency). Moreover, there was also no significant difference in the genotype distribution or allele frequencies among the three stroke subgroups (b allele frequency: 0.889 for atherothrombotic stroke; 0.862 for lacunar stroke; 0.853 for silent lacunar stroke). These findings suggest that there is no overt association between this ecNOS gene polymorphism and ischemic stroke. We found no evidence that this polymorphism may be a genetic factor for the onset of cerebrovascular disease in this Japanese population.
由内皮型一氧化氮合酶(ecNOS)生成的内皮源性一氧化氮介导内皮依赖性血管舒张和抗血栓作用。我们分析了127例缺血性脑卒中患者(18例动脉粥样硬化血栓形成性、58例腔隙性、51例无症状腔隙性脑卒中)和91例对照者中ecNOS基因多态性(第4内含子27bp重复序列)的分布情况。当我们将四个重复序列指定为等位基因a,五个重复序列指定为等位基因b时,卒中组和对照组的基因型分布及等位基因频率之间无显著差异(b等位基因频率分别为0.862和0.868)。此外,三个卒中亚组之间的基因型分布或等位基因频率也无显著差异(b等位基因频率:动脉粥样硬化血栓形成性卒中为0.889;腔隙性卒中为0.862;无症状腔隙性卒中为0.853)。这些发现提示该ecNOS基因多态性与缺血性脑卒中之间无明显关联。我们没有发现证据表明这种多态性可能是该日本人群脑血管病发病的遗传因素。