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SCNN1A基因多态性与氢氯噻嗪降压疗效的相关性 被引量:1

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摘要 目的探讨上皮细胞钠通道α亚基(SCNN1A)基因单核苷酸多态性位点rs2228576与氢氯噻嗪降压疗效的相关性。方法选取新发的轻中度原发性高血压患者110例,均来自吉首市的常住苗族人群。予以氢氯噻嗪口服治疗8周,对降压疗效进行评定。用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术分析患者SCNN1A基因rs2228576多态性的分布频率。结果 EH患者存在三个基因型(AA、AG及GG),频率分别为(0.127,0.509,0.364)。rs2228576位点不同基因型与经DHCT治疗后DBP的降低幅度有关,降压疗效间差异有统计学意义(F=11.522,P<0.05),收缩压降低幅度间无统计学意义(F=2.841,P>0.05)。结论 SCNN1A基因rs3828942多态性可能与DHCT的降压疗效有关。
出处 《中国医药指南》 2013年第31期165-166,共2页 Guide of China Medicine
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参考文献8

  • 1Butterworth MB. Regulation of the epithelial sodium channel (ENaC) by membrane trafficking[J]. Biochim Biophys Acta,2010, 1802(12):1166-1177.
  • 2Butterworth MB,Edinger RS,Frizzell RA,et al. Regulation of the epithelial sodium channel by membrane trafficking[J]. Am J Physiol Renal Physiol,2009,296(1):F 10-F24.
  • 3向波,王晓春,周明欢,张业军,钟飞,陈正英,周卫华,彭湘萍,符自清,李文悌.SCNN1A基因多态性与土家族、苗族及汉族人群原发性高血压相关性的研究[J].临床心血管病杂志,2011,27(10):783-786. 被引量:4
  • 4刘洁琳,刘雅,王佐广,王皓,李梅,王丽娟,温绍君.WNK1基因多态性与血管紧张素转换酶抑制剂降压疗效的相关性研究[J].中国全科医学,2013,16(4):392-395. 被引量:4
  • 5Samaha FF,Rubenstein RC,Yan W, et al. Functional polymorphism in the carboxyl terminus of the alpha-subunit of the human epithelial sodium channel[J].J Biol Chem,2004,279(23):23900- 23907.
  • 6Yan W, Suaud L,Kleyman TR,et al. Differential modulation of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel by protein kinase Cdelta[J]. Am J Physiol Renal Physiol,2006,290(2):F279-F288.
  • 7Ambrosius WT, Bloem LJ,Zhou L,et al. Genetic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension [J].Hypertension, 1999,34(4ptl): 631-637.
  • 8Sugiyama T, Kato N,Ishinagaa Y, et al. Evaluation of selected poly- morphisms of the Mendelian hypertensive disease genes in the Japanese population[J].Hypertens Res,2001,24(5):515-521.

二级参考文献22

  • 1徐红,李南方,洪静,张丽,周玲,李涛,欧阳玮琎,成秋燕.上皮细胞钠通道α亚单位基因4种单核苷酸多态性与新疆哈萨克族人原发性高血压的相关性[J].中国医学科学院学报,2009,31(6):740-745. 被引量:7
  • 2LOFFING J, SCHILD L. Functional Domains of the Epithelial Sodium Channel [J].J Am Soc Nephrol, 2005,16:3175-3181.
  • 3BUTTERWORTH M B. Regulation of the epithelial sodium channel (ENaC) by membrane trafficking[J].Biochim Biophys Acta, 2010,1802 : 1166- 1177.
  • 4HANUKOGLU A, EDELHEIT O, SHRIKI Y, et al. Renin-aldosterone response, urinary Na/K ratio and growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) subunit genes[J].J Steroid Biochem Mol Biol, 2008,111: 268-274.
  • 5ALVAREZ DE LA ROSA D, CANESSA C M, FY FE G K, et al. Structure and regulation of amiloride- sensitive sodium channels [J]. Annu Rev Physiol, 2000,62:573-594.
  • 6BUTTERWORTH M B, EDINGER R S, FRIZZELL R A, et al. Regulation of the epithelial sodium chan- nel by membrane trafficking[J]. Am J Physiol Renal Physiol, 2009,296 : F10 - F24.
  • 7SAMAHA F F, RUBENSTEIN R C, YAN W, et al. Functional polymorphism in the carboxyl terminus of the alpha-subunit of the human epithelial sodium channel[J]. J Biol Chem, 2004,279 : 23900- 23907.
  • 8YAN W, SUAUD L, KLEYMAN T R, et al. Differ- ential modulation of a polymorphism in the COOH terminus of the alpha-subunit of the human epithelial sodium channel by protein kinase Cdelta[J]. Am J Physiol Renal Physiol, 2006,290 : F279 - F288.
  • 9AMBROSIUS W T, BLOEM L J, ZHOU L, et al. Ge netic variants in the epithelial sodium channel in relation to aldosterone and potassium excretion and risk for hypertension[J]. Hypertension, 1999,34 : 631 - 637.
  • 10SUGIYAMA T, KATO N, ISHINAGAA Y, et al. Evaluation of selected polymorphisms of the Mende- lian hypertensive disease genes in the Japanese popula tion[J]. Hypertens Res,2001,24:515-521.

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