摘要
目的探讨血管紧张素转换酶(ACE)基因插入(I)/缺失(D)多态性与阳性卒中家族史(FHS)性脑卒中的相关性。方法采用聚合酶链反应技术(PCR)技术检测47例阳性FHS和145例阴性FHS脑卒中患者的ACE基因插入和缺失多态性。结果阳性FHS组的D等位基因频率(0.72)明显高于阴性FHS组(0.52),P<0.05。DD基因型也明显高于阴性FHS组(51.5%vs23.5%,x2=12.84,P<0.001)。结论认为ACE基因缺失多态性在阳性FHS性脑卒中的形成中可能起重要作用。
Objective To study the relationship between insertion (I)/deletion(D) polymorphisms of angiotension converting enzyme (ACE) gene and stroke with positive family history of stroke(FHS).Methods ACE gene polymorphisms of 47 stroke subjects with positive FHS and 145 subjects with negative FHS were identified by PCR.Results D allele frequency (0.72) in positive FHS group was significantly higher than that in negative FHS group (0.46), P <0.05.ACE DD genotype in positive FHS group was also more common than that in negative FHS group (51.1% vs 23.5%), P <0.001.Conclusion Deletion polymorphism of ACE gene might play an important role in the development of stroke with positive FHS.