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机构地区:[1]包头医学院第一附属医院神经内科,内蒙古包头014010
出 处:《包头医学院学报》2015年第7期9-11,共3页Journal of Baotou Medical College
基 金:包头市医药卫生科技计划项目(wsjj2013089)
摘 要:目的:探讨细胞周期依赖性激酶抑制基因(cyclin dependent kinase inhibitors,CDKN2B)多态性及其与脑梗死发病的关系。方法:以rs3217992位点为遗传标记,采用聚合酶链式反应和限制性片段长度多态性(PCR-RFLP)方法检测180例脑梗死患者和120例对照者的基因型,用Logistic回归分析基因多态性与脑梗死的关系。结果:脑梗死组A等位基因频率较对照组增高(χ2=33.568,P<0.001),脑梗死组AG+AA基因型频率较对照组增高(χ2=28.755,P<0.001),Logistic回归分析显示CDKN2B基因rs3217992位点AG+AA基因型是脑梗死发病的独立危险因素。结论:CDKN2B基因rs3217992位点多态性与脑梗死的发病可能有关,AG+AA基因型为脑梗死患者发病的独立危险因素。Objective: To investigate cyclin-dependent kinase inhibitor 2B( CDKN2B) polymorphism and its association with cerebral infarction. Methods: 180 patients with cerebral infarction were recruited into this study,and 120 healthy people were included as controls. SNP rs3217992 was used as the genetic marker. PCR-based restriction fragment length polymorphism analysis was applied to detect the genotype rs3217992 in the two groups,and the association between CDKN2 B polymorphism and cerebral infarction was analyzed using logistic regression.Results: The frequency of allele A and AG + AA genotype was significantly higher in cases than that in controls( χ2= 33. 568,P〈0. 001)( χ2=28. 755,P〈0. 001). Logistic regression analysis suggested that AG + AA genotype in CDKN2 B rs3217992 was the independent risk factor of cerebral infarction. Conclusion: CDKN2 B polymorphism of rs3217992 is likely to contribute to the etiology of cerebral infarction. AG + AA genotype may be the independent risk factor of cerebral infarction.
关 键 词:细胞周期依赖性激酶抑制基因 单核苷酸多态性 脑梗死
分 类 号:R743.3[医药卫生—神经病学与精神病学]
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