摘要
目的探讨人类血管紧张素转换酶(ACE)基因插入/缺失多态性(I/D)与2型糖尿病(T2DM)患者股动脉内中膜厚度(FA-IMT)的关系。方法采用限制性片段长度多形态多聚酶链式反应(PCR-RFLP)技术检测了303例T2DM患者和93例健康个体ACE基因内含子16插入/缺失(I/D)多态性,利用B型超声检测T2DM患者FA-IMT的情况。结果与健康对照组比较,T2DM患者I等位基因频率显著增高,而D等位基因频率显著降低。携带ACE DD基因型者FA-IMT增厚的比例显著高于携带II及ID基因型者(P<0.01);多元线性逐步回归分析显示,与T2DM患者基线FA-IMT关系密切的指标为年龄、ACE DD基因型、饮酒史。结论ACE DD基因型是T2DM患者FA-IMT增加的独立的危险因素。
Objective To investigate the relationship between angiotensin Ⅰ-converting enzyme(ACE) inserting/defaulting (I/D) gene polymorphisms and the femoral artery intima -media thickness (FA-IMT) in patients with type 2 diabetes mellitus (T2DM). Methods The polymorphisms of ACE (I/D) was determined by polymerase chain reaction-restriction fragment length polymorphism ( PCR - RFLP) method and the FA-IMT was assessed using non - invasive high resolution B-mode uhrasonography in 303 patients with T2DM in Hunan province. Results The frequency of I allele of ACE gene polymorphisms was higher in T2DM than that in healthy controls, but frequency of D allele was lower in T2DM than that in healthy controls(P〈0.05). Patients with ACE DD genotype had higher FA-IMT than those with ACE II or ACE ID genotype(P〈0.01). Multivariate linear regression analysis showed that age, alcohol intake and ACE DD genotype were closely correlated with the FA-IMT in T2DM patients. Conclusion The ACE I/D gene polymorphism was a inhered risk factor for T2DM development and ACE DD genotype was one of the independent risk factors for FA-IMT in T2DM patients.
出处
《中国医师杂志》
CAS
2005年第10期1304-1306,共3页
Journal of Chinese Physician
基金
国家十五科技攻关资助项目(2001BA702B01
2001BA702B04)
湖南省科技资助项目(02SSY3065)