摘要
目的 :了解血管紧张素转换酶 (ACE)基因多态性与新疆地区原发性高血压的易感相关性。方法:应用聚合酶链反应 (PCR)对 78例新疆地区原发性高血压患者与 72例正常血压对照者 ACE基因第 16内含子插入 /缺失多态性进行鉴定。结果:在新疆地区原发性高血压患者中 ,ACE基因缺失纯合基因型 (DD)和缺失 (D)等位基因频率均明显高于正常血压者 (P <0 .0 5及 P <0 .0 1)。
Objective: To asses whether the insertion/deletion(I/D) polymorphism of angiotensin coverting enzyme (ACE) gene was associated with essential hypertension in xinjiang. Methods: I/D polymorphism of ACE was determined by polymerase chain reaction (PCR) in 72 normal controls, 78 patients with essential hypertension. Results: The frequencies of DD gene type (0.30) and deletion allele (0.53) among essential hypertension were significantly higher than those (0.14) among control subjects (0.375). Conclusion: The results indicate that a deletion polymorphism of ACE gene probably may be the risk factor in essential hypertension in xinjiang.
出处
《新疆医科大学学报》
CAS
2003年第2期143-145,共3页
Journal of Xinjiang Medical University
基金
新疆医科大学第一附属医院硕士启动基因项目 (98-XYQD-0 5 )