谷胱甘肽过氧化物酶1基因多态性与川崎病的关联性分析
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湖南省自然科学基金(12JJ3108)


Association of Glutathione Peroxidase-1 Gene Polymorphism with Kawasaki Disease
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    摘要:

    目的 探讨谷胱甘肽过氧化物酶1(GPX-1)基因多态性与中国汉族儿童川崎病(kawasaki disease,KD)并冠状动脉损害(CAL)的相关性。方法 采用聚合酶链反应-限制性内切酶片段长度多态性分析(PCR-RFLP)检测92例川崎病患儿及108例健康儿童GPX-1基因的-46C/T位点和599C/T位点多态性。结果 川崎病组GPX-1基因-46C/T位点CC、CT、TT基因型分布和C、T等位基因频率与正常对照组比较差异无显著性意义(χ2 0.174和0.166,P均>0.05)。川崎病组GPX-1基因599C/T位点CC、CT、TT基因型分布和C、T等位基因频率与正常对照组比较差异亦无显著性意义(χ20.429和0.368,P均>0.05)。川崎病患儿合并CAL组与无冠状动脉损害(NCAL)组GPX-1基因-46C/T位点基因型分布和等位基因频率比较差异亦无显著性意义(χ20.507和0.487,P均>0.05)。川崎病患儿合并CAL组与NCAL组GPX-1基因599C/T位点基因型分布和等位基因频率比较差异亦无显著性意义(χ20.635和0.535,P均>0.05)。结论 尚未发现GPX-1基因-46C/T位点多态性以及599C/T位点多态性与川崎病及其CAL的发生存在明显关联性。

    Abstract:

    Aim To investigate the genetic association of glutathione peroxidase-1(GPX-1) gene polymorphism in patients with kawasaki disease (KD),and coronary artery lesions (CAL). Methods There were 92 patients with KD and 108 healthy subjects in this study. The genotype of locus -46C/T and locus 599C/T of GPX-1 were detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Results For -46C/T polymorphism and 599C/T polymorphism in GPX-1 gene,there were no significant differences between KD patients and the controls in genotype frequencies of CC,CT and TT,and allele frequencies of C and T (χ20.174 and 0.166,both P>0.05 χ20.429 and 0.368,both P>0.05) For -46C/T polymorphism and 599C/T polymorphism in GPX-1 gene,there were no significant differences between KD patients with CAL and without CAL in genotype and allele frequencies of C and T (χ20.507 and 0.487,both P>0.05 χ20.635 and 0.535,both P>0.05). Conclusion No association was found in -46C/T polymorphism and 599C/T polymorphism between GPX-1 gene and the risk of KD or its complication of CAL in this study.

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陈 芳,江 杰,李卓颖,陈 佳,田 朗,李 欣,伍志翔,黄利华,杨作成.谷胱甘肽过氧化物酶1基因多态性与川崎病的关联性分析[J].中国动脉硬化杂志,2015,23(03):290~294.

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  • 收稿日期:2014-04-28
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