期刊文献+

血管紧张素原基因M235T多态性和房颤传统危险因素的交互作用 被引量:3

下载PDF
导出
摘要 目的分析血管紧张素原基因M235T多态性和房颤传统危险因素的联系。方法采用聚合酶链反应及限制性片段长度多态性技术检测250例房颤患者和200例健康体检者的M235T多态性;Logistic回归分析研究房颤的独立危险因素;叉生分析表法研究AGT基因M235T多态性与房颤传统风险因素的交互作用。结果Logistic回归分析显示AGT基因M235T多态性TT基因型携带者增加了患房颤的危险(OR=2.02,95%CI=1.14—2.56)。叉生分析表结果显示M235T多态性TT型携带者与患脑梗死或高血压存在正交互作用。结论针对中国汉族人群,M235T多态性和房颤传统危险因素(脑梗死、高血压)能协同增加房颤的风险。
作者 王成
出处 《中国老年学杂志》 CAS CSCD 北大核心 2013年第18期4441-4443,共3页 Chinese Journal of Gerontology
  • 相关文献

参考文献11

  • 1Topal NP, Ozben B, Hancer VS,et al. Polymorphisms of the angiotensin- converting enzyme and angiotensinogen gene in patients with atrial fibril- lation[J]. J Renin Angiotensin Aldosterone Syst,2011 ;12(4) :549-56.
  • 2Tsai CT, Lai LP, Lin JL, et al. Renin-Angiotensin system gene polymor- phisms and atrial fibrillation [ J ]. Circulation,2004 ; 109 ( 13 ) : 1640-6.
  • 3Freitas AI, Mendonca I, Brian M, et al. RAS gene polymorphisms, classi- cal risk factors and the advent of coronary artery disease in the Portuguese population [ J ]. B MC Cardiovascular Disorders, 2008 ; 8 ( 15 ) : 1471-2261.
  • 4Niemiec P,Zak I, Wita K. The M235T polymorphism of the AGT gene modifies the risk of coronary artery disease associated with the presence of hypercholesterolemia[J]. Eur J Epidemio1,2008 ;23 (5) :349-54.
  • 5Zhou GY. On the Estimation of additive interaction by use of the four-by-two table and beyond[J]. Am J Epidemiol,2008 ;168 :212-24.
  • 6吴志勤,陈庆伟,吴庆,柯大智,李兴升,李桂琼,王鹏.血清脂蛋白a与冠心病的研究[J].重庆医科大学学报,2011,36(11):1356-1360. 被引量:34
  • 7李虹,杨军,苏锐,肖传实,高奋.DDAH2基因多态性与冠心病的相关性研究[J].重庆医科大学学报,2010,35(10):1490-1493. 被引量:1
  • 8杜艳蕾,聂玉强,李瑜元,石胜利,詹琪,周永健.PEMT基因V175M多态性与非酒精性脂肪肝易感性的关系[J].现代生物医学进展,2008,8(11):2021-2023. 被引量:1
  • 9高霞,薛鹏,李涛,杨海涛.叉生分析在交互作用研究中的应用[J].临床荟萃,2009,24(17). 被引量:1
  • 10Ruch RJ,Trosko JE,Madhukar BV. Inhibition of connex in43 gap junc- tional intercellular communication by TPA requires ERK activation [ J]. J Cell Biochem ,2001 ;83 ( 1 ) : 163-9.

二级参考文献28

  • 1毛念新,黄叶肖,陆卫,叶红娟,沈学础,胡志宏,罗安湘.天然FeS_2(黄铁矿)的红外光谱研究[J].物理学报,1993,42(10):1712-1718. 被引量:4
  • 2杜艳蕾,石胜利,聂玉强,李瑜元,周永健.非肥胖者发生非酒精性脂肪肝的预测指标[J].现代生物医学进展,2006,6(10):70-72. 被引量:3
  • 3Leiper J M,Santa Maria J,Chubb A,et al. Identification of two human dimethylarginine dimethylaminohydrolases with distinct tissue distributions and homology with microbial arginine deiminases[J].Biochem J, 1999,1 (343) : 209-214.
  • 4Anthony S, Leiper J,Vallance P. Endogenous production of nitric oxide synthase inhibitors[J].Vasc Med, 2005,10( s1):3-9.
  • 5Maas R. Pharmacotherapies and their influence on asymmetric dimethylargine (ADMA) [J]. Vasc Med, 2005,10 (s1): 49-57.
  • 6Dayoub H,Achan V,Adimoolam S,et al.Dimethylarginine dimethylaminohydrolase regulates nitric oxide synthesis[J].Circulation,2003,108: 1043-1048.
  • 7Leiper J,Nandi M,Torondel B,et al.Disruption of methylarginine metabolism impairs vascular homeostasis[J].Nat Med, 2007, 13 ( 2 ) : 198- 203.
  • 8Tatematsu S,Wakino S,Kanda T,et al. Role of nitric oxide-producing and -degrading pathways in coronary endothelial dysfunction in chronic kidney disease[J]. J Am Soc Nephrol, 2007, 18( 3 ) : 741-749.
  • 9Jones L C,Tran C T L, Leiper J M,et al. Common genetic variation in a basal promoter element alters DDAH2 expression in endothelial cells[J]. Biochem Biophys Res Commun, 2003,310(3 ) : 836-843.
  • 10O' Dwyer M J, Dempsey F, Crowley V,et al. Septic shock is correlated with asymmetrical dimethyl arginine levels, which may be influenced by a polymorphism in the dimethylarginine dimethylaminohydrolase II gene : aprospective observational study[J]. Crit Care, 2006,10( 5 ) : 139.

共引文献33

同被引文献56

  • 1周自强,胡大一,陈捷,张仁汉,李奎宝,赵秀丽.中国心房颤动现状的流行病学研究[J].中华内科杂志,2004,43(7):491-494. 被引量:1401
  • 2Chen Y,Wu Z, Yang C, et al. Investigation of atrial vulnerabili- ty by analysis of the sinus node EG from atrial fibrillation mod- els using a phase synchronization method[J]. IEEE Transac- tions on Biomedical Engineering,2012,59(9):2668-2676.
  • 3Gurrapu A, Jukanti R, Bobbala SR,et al. Improved oral deliv- ery of valsartan from maltodextrin based proniosome powders[J]. Advanced Powder Technology,2012,23(5) :583-590.
  • 4Thibodeau IL, Xu J, Li Q, et al. Paradigm of genetic mosaicism and lone atrial fibrillation: physiological characterization of a connexin 43-deletion mutant identified from atrial tissue[J]. .i Circulation, 2010,122(3) : 236-244.
  • 5Hagendorff A, Schumacher B, Kirchhoff S,et al . Conduction disturbances and increased atrial vulnerability in Connexin40- deficient mice analyzed by transesophageal stimulation[J]. Cir- culation,1999 ,99(11) :1508-1515.
  • 6Yang YQ, Liu X, Zhang XL,et al. Novel connexin40 missense mutations in patients with familial atrial fibrillation[J]. Eu- ropaee, 2010,12(10) : 1421-1427.
  • 7Yang YQ, Zhang XL, Wang XH,et al. Connexin40 nonsense mutation in familial atrial fibrillation[J]. Int J Mol Med,2010,26(4) : 605-610.
  • 8Igarashi T, Finet JE, Takeuchi A, et al. Connexin Gene Transfer Preserves Conduction Velocity and Prevents Atrial Fibrillation [J]. Circulation,2011,125(2) :216-225.
  • 9Rack'auskas M, Neverall-Skas V, Skeberdis VA. Diversity and properties of connexin gap junction channels[J]. Medicina, 2010,46(1) :1-12.
  • 10Jansen JA, Van Veen TA, de Bakker JM,et al. Cardial con- nexins and impulse propagation[J].J Mol Cell Cardiol, 2010, 48(1), 76-82.

引证文献3

二级引证文献11

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