摘要
以血管紧张素Ⅰ转化酶(ACE)基因为候选基因,随机挑选135例NIDDM患者和57例正常人,用PCR方法检测ACE基因的缺失/插入多态性。结果发现研究人群的ACE基因型分布趋势与法国白种人群一致,而与日本人群的分布趋势显著不同。ACE基因的几种基因型均与NIDDM伴发高血压无相关关系。但D等位基因与NIDDM患者具有典型心肌缺血的异常心电图表现显著相关,D/D基因型在该组有异常心电图表现的NIDDM患者中频率明显增高,提示携带该基因型的患者具有冠心病易感性。在NIDDM患者中进行ACE基因型检查有助于对冠心病的早期诊断和治疗。
Diabetes mellitus,hypertension and coronary heart disease (CHD)are polygenetic
diseases which have common genetic back-ground.The incidence of cardiovascular diseases ill
diabetes is higher than that in general population.Our study takes the an-giotensin Ⅰconverting
enzyme gene as a candidate gene,and detect the deletion/insertion polymorphism of ACE gene
by PCRmethed in 135 NIDDM patients and 57 controls.We found the distribution of genotypes in
our population is the same as that ofCaucasian population, but is different from Japanese
population. There is no association between the polymorphism of ACE geneand hypertension
in NIDDM patients in our study. We found that the D allele is associated with abnormal EKG in
NIDDM patients. The frequency of DD genotype in this group is higher than that in patients
without abnormal EKG. So this result shows that NID-DM patients whose genotypes are DD
have the susceptibility for CHD. That this polymorphism is of interest in primary preventionand
detection of CHD in NIDDM,particular for patients carring the DD genotype.
出处
《中华内分泌代谢杂志》
CAS
CSCD
北大核心
1995年第4期197-200,共4页
Chinese Journal of Endocrinology and Metabolism