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首页> 外文期刊>International Journal of Neuroscience >Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine
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Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine

机译:神经元一氧化氮合酶基因的C276T多态性与偏头痛之间缺乏关联

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摘要

A migraine attack is a spectacularly complex brain event that can produce a wide array of neurological and systemic symptoms. The molecular mechanisms and genetics of migraine have not yet been clarified. The objective of this study was to analyze the genotype distributions and allele frequencies for the C276T polymorphism of the neuronal nitric oxide synthase (nNOS) gene among the patients with migraine. The diagnosis of migraine was made clinically based on questionnaires. One hundred and twenty patients with migraine were genotyped for the C276T polymorphism of the nNOS gene and compared with 185 age-matched healthy controls. Genomic DNA from migraine patients and controls was analyzed by polymerase chain reaction (PCR). A PCR-restriction fragment-length polymorphism analysis of nNOS gene polymorphism was performed, and the results were compared. Neither genotype distributions nor the allele frequencies for the C276T polymorphism showed a significant difference between the groups. Additionally, there was no marked differences in genotype distribution or allele frequencies for the migraine without aura and migraine with aura subgroups when compared to control group. These results suggested that migraine of the Turkish population seemed to develop without any alterations in nNOS C276T polymorphism. Our data showed that there is no marked association between the C276T polymorphism of the nNOS gene and migraine.
机译:偏头痛发作是一种极为复杂的大脑事件,可产生多种神经系统症状和全身症状。偏头痛的分子机制和遗传学尚未阐明。这项研究的目的是分析偏头痛患者中神经元型一氧化氮合酶(nNOS)基因C276T多态性的基因型分布和等位基因频率。偏头痛的诊断是根据问卷进行临床诊断的。对120例偏头痛患者的nNOS基因C276T多态性进行了基因分型,并与185个年龄相匹配的健康对照组进行了比较。通过聚合酶链反应(PCR)分析了偏头痛患者和对照组的基因组DNA。进行了nNOS基因多态性的PCR限制性片段长度多态性分析,并对结果进行了比较。 C276T多态性的基因型分布和等位基因频率均未显示两组之间的显着差异。此外,与对照组相比,无先兆偏头痛和先兆亚组偏头痛的基因型分布或等位基因频率无明显差异。这些结果表明,土耳其人群的偏头痛似乎在nNOS C276T多态性没有任何改变的情况下发展。我们的数据表明,nNOS基因的C276T多态性与偏头痛之间没有明显的关联。

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