摘要
目的探讨人血管紧张素转换酶(ACE)基因插入/缺失多态性(I/D)与新诊断2型糖尿病(T2DM)患者颈总动脉内中膜厚度(CCA-IMT)的关系。方法采用限制性片段长度多态性-聚合酶链反应(PCR-RFLP)技术,检测2005年5月至2006年5月东莞市人民医院内分泌门诊收治的120例T2DM患者ACE基因内含子16I/D多态性,利用B超检测其CCA-IMT,通过多元Logistic回归分析筛选T2DM患者CCA-IMT增厚的危险因素。结果携带ACE基因DD型者CCA-IMT增厚的比例显著高于携带II及ID基因型者(F=10.164,P=0.006);Logistic回归分析显示,ACEDD基因型、年龄、合并高血压是T2DM患者CCA-IMT增厚的危险因素(OR分别为3.689,1.054,1.562,P均<0.05)。结论ACEDD基因型是T2DM患者CCA-IMT增厚的独立危险因素。
Objective To investigate the relationship between angiotensin l-converting enzyme(ACE)inserting/defaulting(I/D )gene polymorphisms and the carotid intima-media thickness (CCA-IMT)in patients with type 2 diabetes (T2DM). Methods The polymorphisms of ACE(I/D) was determined by polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP)method and the CCA-IMT was assessed using non-invasive high resolution B-mode ul- trasonography in 120 T2DM in Han's population of Dongguan city. The data were analyzed by Logistic regression to explore the independent and significant risk factors for CCA-IMT increase in type 2 diabetic patients. Results The DD genotype were significantly more common in diabetic patients with CCA-IMT increase than in those without it( F = 10. 164,P = 0. 006) ; Logistic regression analysis showed that DD genotype, age, male gender and essential hypertension contributed significantly to the CCA-IMT increase in type 2 diabetic patients ( OR = 3. 689,1. 054,1. 562, respectively, P 〈 0.05 ). Conclusion DD genotype is an independent risk factor for CCA-IMT increase in type 2 diabetic patients.
出处
《中国实用内科杂志》
CAS
CSCD
北大核心
2007年第16期1304-1305,共2页
Chinese Journal of Practical Internal Medicine
关键词
2型糖尿病
颈总动脉内中膜厚度
基因多态性
血管紧张素转换酶基因
Type 2 diabetes mellitus
Carotid intima-media thickness
Gene polymorphism
Angiotensin 1 -converting enzyme gene