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作 者:陈煜森[1] 曾志良[1,2] 林智君[1] 冼文川[1] 钟望涛[1] 赵斌[1] 许志恩[1]
机构地区:[1]广东医学院附属医院神经内科,广东湛江市524001 [2]东莞市太平人民医院,广东东莞市523900
出 处:《中国康复理论与实践》2012年第5期406-408,共3页Chinese Journal of Rehabilitation Theory and Practice
基 金:教育部留学回国人员科研启动基金(教外司留[2005]546号)
摘 要:目的分析中国汉族人群凝血酶激活纤溶抑制物基因启动子区-438A/G(TAFI-438A/G)多态性与动脉粥样硬化性脑梗死(ACI)发病的关系。方法 225例ACI患者(病例组)和184例健康体检者(对照组)采用聚合酶链反应-限制性内切酶片段长度多态性分析方法(PCR-RFLP)检测TAFI-438A/G多态性。结果 TAFI-438A/G基因型及等位基因频率在病例组与对照组之间无显著性差异。性别分层后,男性脑梗死组A等位基因频率为28.6%,高于对照组20.6%(P=0.039);AA基因型为9.0%,高于对照组1.9%(P=0.019);在女性中无显著性差异。结论 TAFI-438A/G可能与男性脑梗死的发病有关,AA基因型可能增加男性脑梗死患病风险。Objective To research the relationship between promoter polymorphism-438 A/G of thrombin-activatable fibrinolysis inhibi- tor gene (TAFI-438 A/G) and atherosclerotic cerebral infarction (ACI) in Chinese Han population. Methods TAFI-438A/G genotypes and their allele frequencies were identified with the polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) in 225 ACI patients and 184 healthy controls. Results There was no significant difference of TAFI-438A/G polymorphism between ACI group and control group. Stratified by gender, in males, the incidence of A allele was 28.6% in ACI group, and 20.6% in control (P=0.039); of the AA genotype was 9.0% in ACI group, and 1.9% in control (P=0.019). But no significant difference was found in females. Conclusion TAFI-438A/G polymorphism is associated with the risk of ACI in males, that AA genotype may increase the risk of ACl.
关 键 词:凝血酶激活纤溶抑制物 启动子 基因多态性 动脉粥样硬化 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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