摘要
目的:研究凝血酶激活的纤溶抑制物(TAFI)编码区CPB2基因位点C1040T和G505A的单核苷酸多态性与脑梗死之间的联系。方法:应用聚合酶链反应和限制性内切酶片段长度多态性分析技术(PCR-RFLP)检测98例脑梗死患者和100名正常对照者的TAFI基因编码区C1040T(Thr325Ile)、G505A(Thr147Ala)多态性分布特点。结果:CPB2基因C1040T(Thr325Ile)及G505A(Thr147Ala)2个位点的3种基因型在脑梗死组和对照组的频率分布分别为C1040C(Thr325Thr)33(33.7%)、29(29.0%);C1040T(Thr325Ile)47(48.0%)、51(51.0%);T1040T(Ile325Ile)18(18.3%)、20(20.0%);A505A(Thr147Thr)15(15.3%)、43(43.0%);G505A(Thr147Ala)44(45.0%)、19(19.0%);G505G(Ala147 Ala)39(39.7%)、38(38.0%)。经χ2检验,基因型分布符合Hardy-Weinberg平衡,并且脑梗死组与对照组之间各种基因型频率分布差异无统计学意义(P>0.05)。结论:TAFI编码区CPB2基因(Thr325Ile、Thr147Ala)的多态性与脑梗死的发生无明显相关性。
Objective: To investigate the polymorphism of thrombin-activatable fibrinolysis inhibitor(TAFI)encoding gene CPB2 in patients with cerebral infarction(CI).Methods: CPB2 gene(Thr325Ile and Thr147Ala)polymorphism was typed with polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) in patients with CI(n=98) and a control group(n=100).Results: The genotype frequencies of Thr325Ile(C1040T) and Thr147Ala(G505A) in the CI group and control group were as follows: C1040C(Thr325Thr)of 33(33.7%)and 29(29.0%);C1040T(Thr325Ile)of 47(48.0%)and 51(51.0%);T1040T(Ile325Ile)of 18(18.3%)and 20(20.0%);A505A(Thr147Thr)of 15(15.3%)and 43(43.0%);G505A(Thr147Ala) of 44(45.0%)and 19(19.0%);and G505G(Ala147 Ala)of 39(39.7%)and 38(38.0%).χ2 analysis showed no significant difference in all the Thr325Ile and Thr147Ala polymorphism distributions in the CI and control groups(P0.05).Conclusion: None of the results showed any statistical correlation between TAFI polymorphisms and CI.
出处
《浙江中西医结合杂志》
2011年第3期149-152,共4页
Zhejiang Journal of Integrated Traditional Chinese and Western Medicine
关键词
脑梗死
凝血酶激活的纤溶抑制物
PCR-RFLP
CPB2基因
单核苷酸多态性
cerebral infarction thrombin-activatable fibrinolysis inhibitor(TAFI)polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) CPB2 gene polymorphism