期刊文献+

山西地区血管紧张素原基因和α-内收蛋白基因多态性与原发性高血压的相关性研究 被引量:6

Association study of genetic polymorphisms of alpha-adducin and angiotensinogen with essential hypertension in Shanxi population
原文传递
导出
摘要 目的调查山西地区血管紧张素原(angiotensinogen,AGT)和α-内收蛋白(alpha-aduction,ADD1)基因多态性与原发性高血压(essential hypertension,EH)的关系。方法采用病例对照研究,用诱变分离聚合酶链反应(mutagenically separated polymerase chain reactions,MS-PCR)检测山西地区EH患者299例(病例组)和血压正常者218例(对照组)的AGT基因M235T多态性和ADD1基因Gly460Trp多态性。结果病例组AGT基因的TT基因型分布与对照组差异有统计学意义(P<0.001),但病例组T等位基因频率(0.426)与对照组(0.378)相比,差异无统计学意义(P=0.121)。病例组ADD1基因型分布和等位基因频率与对照组相比,差异均无统计学意义(P分别为0.306和0.072)。TT+TT联合基因型患EH的危险度增加(MT+GG:OR=0.410,P=0.041;MT+GT:OR=0.364,P=0.020;MT+TT:OR=0.262,P=0.002)。Logistic回归分析提示,AGT基因的TT基因型较MM、MT基因型患EH的相对危险度增加(MM:OR=0.502,P=0.019;MT:OR=0.306,P<0.001)。结论 AGT M235T多态性与山西地区人群患EH相关,TT基因型可能与EH危险增加有关。AGT M235T多态性与ADD1基因Gly460Trp多态性间存在基因间的协同作用。 Objective This case-control study was designed to investigate the association between angiotensinogen gene polymorphisms and alpha-adducin polymorphisms and essential hypertension (EH). Methods A case-control study was conducted using performed mutagenically separated polymerase chain reactions (MS-PCR) techniques to explore the AGT gene M235T polymorphisms and the ADD1 gene Gly460Trp polymorphisms in 299 EH and 218 normotensives (NT) of Shanxi Province. Results The genotypes distribution of TT in EH cases was significantly higher than in NH cases ( P〈 0. 001 ), but not the alletic frequency of T (0. 426 vs. 0. 378, P = 0. 121 ). No significant difference were seen in the genotype distribution and the alletic frequency of ADD1 gene between EH and NH cases (P = 0. 306, P = 0. 072). The genotype distribution of TT + TTT was significantly higher to get EH. ( MT + C/G: OR = 0. 410, P = 0. 041 ; MT + GT- OR = 0. 364, P = 0. 020; MT + TT: OR = 0. 262, P = 0. 002 ). Those who exosed to TT genotype of AGT gene was the easlest to get EH. (MM. OR=0.502, P=0.019;MT:OR=0.306,P〈0. 001). Conclusions TheAGT M235T polymorphism might be associated with Eli in Shanxi population. TT genotype might be associated with the increased risk of EH. ACT M235T polymorphism might have a gene-gene synergetic effect with Gly460Trp polymorphism.
出处 《中华疾病控制杂志》 CAS 2011年第9期740-744,共5页 Chinese Journal of Disease Control & Prevention
基金 山西省科技攻关项目(20080312018)
关键词 高血压 基因型 病例对照研究 Hypertension Genotype Case-control studies
  • 相关文献

参考文献25

二级参考文献117

  • 1刘艳,金玮,姜正文,张奎星,盛海辉,金璘,沈亚云,黄薇,于金德.血管紧张素原基因的六种单核苷酸多态与原发性高血压的相关性[J].中华医学遗传学杂志,2004,21(2):116-119. 被引量:16
  • 2孙晓健,侯晓菲,刘少荣,刘文波,陶志刚,李建远.醛固酮合成酶基因-344T/C多态性与山东省汉族人原发性高血压相关性[J].中华医学遗传学杂志,2004,21(5):502-504. 被引量:33
  • 3Blaustein MP,Zhang J,Chen L,et al.How does salt retention raise blood pressure[J].Am J Physiol Regul Integr Comp Physiol,2006,290(3):514-523. 被引量:1
  • 4Morrison RG,Mills C,Moran AL,et al.A moderately high fat diet promotes salt-sensitive hypertension in obese zucker rats by impairing nitric oxide production[J].Clin Exp Hypertens,2007,29(6):369-381. 被引量:1
  • 5Junemaitre X,Inoue I,Willians C,et al.Haplotype of angiotensinogen in essential hypertension[J].Am J Hum Genet,1997,60(6):1448-1460. 被引量:1
  • 6Sato N,Katsuya T,Rakugi H,et al.Association of variants in critical core promoter element of angiotensinogen gene with increased risk of essential hypertension in Japanese[J].Hypertension,1997,30(3):321-325. 被引量:1
  • 7Beige J,Weber A,Engeli S,et al.Angiotensinogen M235T genotype and post-transplant hypertension[J].Neph Dial Trap,1996,11(8):1538-1541. 被引量:1
  • 8Rotimi C,Morrison L,Cooper R,et al.Angiotensinogen gene in human hypertension:lack of an association of the 235T allele among African Americans[J].Hypertension,1994,24(5):591-594. 被引量:1
  • 9Pereira A C,Mota G F,Cunha R S,et al.Angiotensinogen 235T allele "Dosage" is associated with blood pressure phenotypes[J].Hypertension,2003,41(1):25-30. 被引量:1
  • 10Denton D,Weisinger R,Mundy NI,et al.The effect of increased salt intake on blood pressure of chimpanzees[J].Nat Med,1995,1(10):1009-1016. 被引量:1

共引文献47

同被引文献108

引证文献6

二级引证文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部