医学研究与教育 ›› 2012, Vol. 29 ›› Issue (6): 13-16.

• 临床研究 • 上一篇    下一篇

原发性高血压患者血管紧张素Ⅱ-1型受体基因多态性

王惠凌1,王晓夜1,田红英1,齐晓艳2,张红2,霍玉娥1   

  1. 1.河北大学附属医院,河北保定 071000
    2.保定市第五医院,河北保定 071000
  • 收稿日期:2016-10-09 修回日期:2016-10-09 出版日期:2012-12-25 发布日期:2012-12-25

Association between gene polymorphism of angiotensin-1 receptor and essential hypertension

  • Received:2016-10-09 Revised:2016-10-09 Online:2012-12-25 Published:2012-12-25

摘要: 目的研究血管紧张素Ⅱ-1型受体基因多态位点A1166C与原发性高血压的关系.方法采用聚合酶链反应技术(PCR)对48名40岁以上成人和39例原发性高血压患者血管紧张素Ⅱ-1型受体(AT1R)基因多态性进行检测. 结果 AC基因型、C等位基因频率高血压组与健康人群对照组差别无统计学意义(χ2=0.026、0.023,P>0.05).结论血管紧张素Ⅱ-1型受体基因可能与原发性高血压发病无关.

关键词: 原发性高血压, 基因, 聚合酶链反应, 血管紧张素Ⅱ-1型受体

Abstract: Objective To identify the association between gene polymorphism of A1166C angiotensin, type 1 receptor(AT1R)and essential hypertension(EH). Methods AT1R gene polymorphism was determined by polymerase chain reaction(PCR) in 48 normal controls over aged 40 and 39 cases of EH. Results The AC genotype and C allele were not significantly different between the two groups(χ2=0.026, 0.023, P>0.05). Conclusion The AT1R polymorphism might not be associated with EH.

Key words: essential hypertension(EH), genes, polymerase chain reaction(PCR), angiotensin-1 receptor

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