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糖皮质激素受体基因G1666T多态性与原发性高血压的相关性
引用本文:迟兰芹,张晨,宋明军,孙风翠. 糖皮质激素受体基因G1666T多态性与原发性高血压的相关性[J]. 基础医学与临床, 2006, 26(1): 70-73
作者姓名:迟兰芹  张晨  宋明军  孙风翠
作者单位:烟台市莱阳中心医院,神经内科,山东,莱阳,265200;青岛大学,医学院,附属医院神经内科,山东,青岛,266003
摘    要:目的探讨糖皮质激素受体基因第4内含子基因G1666T多态性与原发性高血压(essential hypertension,EH)的关系。方法用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析71例正常人及48例原发性高血压患者中GR基因第4内含子变异的多态性分布情况。结果从整体来讲,不分性别,GR基因第4内含子的变异在EH与对照组之间,其基因型频率、等位基因的频率无显著性差异。而在女性,与对照组(0.46)比较,EH(0.64)等位基因G的频率明显增高(P<0.05)。结论等位基因G的频率增高可能是原发性高血压的易感基因标志。

关 键 词:高血压  糖皮质激素受体  基因多态性  聚合酶链反应  限制性片段长度多态性
文章编号:1001-6325(2006)01-0070-04
收稿时间:2004-08-12
修稿时间:2005-03-29

Association between glucocorticoid receptor gene G1666T polymorphism and essential hypertension
CHI Lan-qin,ZHANG Chen,SONG Ming-jun,SUN Feng-cui. Association between glucocorticoid receptor gene G1666T polymorphism and essential hypertension[J]. Basic Medical Sciences and Clinics, 2006, 26(1): 70-73
Authors:CHI Lan-qin  ZHANG Chen  SONG Ming-jun  SUN Feng-cui
Affiliation:1. Department of Neurology, Laiyang Central Hospital, Yantal 265200; 2. Department of Neurology, The Affiliated Hospital of Qingdao University Medical College, Qingdao 266003, China
Abstract:Objective To identify the association between human glucocorticoid receptor gene G166T polymorphism and essential hypertension(EH).Methods DNA samples from 71 normotensive cases and 48 EH cases were analyzed by a polymerase chain reaction(PCR) for restriction fragment length polymorphism(RFLP) to determine the intron 4 variant of human glucocorticoid receptor gene.Results No association was observed between EH group and control group.However,in females,a little association was observed between the EH group and control group.Frequencies of allele G were 0.64 in EH group and 0.46 in control group.Conclusion The G allele may be a predisposing gene marker,HGR gene intron 4 polymorphism contributes to the development of EH in females.
Keywords:hypertension  glucocorticoid receptor  gene polymorphism  PCR-RFLP  
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