摘要
应用聚合酶链反应(PCR)技术对非胰岛素依赖型糖尿病(NIDDM)41例、NIDDM合并冠心病51例和正常对照组60例进行载脂蛋白B基因EcoRI和XbaI酶切位点限制性片段长度多态性(RFLP)研究。结果显示少见等位基因频率在NIDDM组及NIDDM并冠心病组均升高。与对照组比较,E-等位基因频率在糖尿病患者显著升高。
The relationship between CHD in NIDDM and apolipoprotein B(apoB) gene polymorphism was studied using polymerase chain reaction and two polymorphic sites of apoB (EcoRI and XbaI) were examined in samples from 41 patients with NIDDM, 51 patients of NIDDM with CHD and 60 healthy individuals as control. The results were as follows: 1. The frequencies of the rarer alleles of the EcoRI and XbaI (E-,X+) were higher in NIDDM with or without CHD. 2. The frequencies of E- alleles were over_represented in NIDDM. 3. The frequencies of X+ alleles were markedly correlated with CHD in NIDDM.
出处
《中华内分泌代谢杂志》
CAS
CSCD
北大核心
1997年第3期137-140,共4页
Chinese Journal of Endocrinology and Metabolism
关键词
Ⅱ型糖尿病
载脂蛋白B
并发症
糖尿病
冠心病
Non_insulindependent diabetes mellitus (NIDDM) Apolipoprotein B gene polymorphism Complication