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加倍剂量福辛普利强化治疗蛋白尿的研究 被引量:1

Effect of Proteinuria Treated with Intensive Double Doses of Fosinopril Therapy
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摘要 目的:研究加倍剂量福辛普利对蛋白尿的强化治疗作用及其安全性。方法:原发性肾病患者随机分为2组,分别给予福辛普利10mg、20mg治疗12周,每3周检测尿蛋白、血压、血钾、血肌酐。结果:①12周后加倍剂量组尿蛋白下降幅度达(57.9±5.1)%,显著高于单倍剂量组(41.5±3.5)% (P<0.01);②两组血压均有显著下降,但两组间无显著差异;③两组血清肌酐、血钾无明显差异。结论:加倍剂量福辛普利较单倍剂量福辛普利有更好的降蛋白尿作用,且加倍剂量对血压能进一步下降但无统计学差异,对肾功能和血钾无不良影响。 Objective:To investigate the antiproteinuric effect and safety of double doses of fosinopril by a randomized controlled study.Methods:The patients with primary glomerular diseases were randomly divided into two groups and used fosinopril in two different dosages(10mg/d and 20mg/d) for 12 weeks.Blood pressure,proteinuria,serum creatinine,and serum potassium were measured every 3 weeks.Results:(1)Double doses of fosinopril exerted more significant aniproteinuric effect compared to the single dose group [(57.9±5.1)% vs(41.5±3.5)%,P0.01] after 12 weeks treatment.(2) The blood preasure reduction between the two groups had no remarkable difference(P0.05).(3)During observation period,serum creatinine and serum potassium in double doses group had no significant increase compared to the single dose group.Conclusion:The double doses of fosinopril had an superior aniproteinuric effect than the single dose and it is secure.
出处 《中国医药导刊》 2012年第1期49-50,共2页 Chinese Journal of Medicinal Guide
关键词 福辛普利 剂量 蛋白尿 原发性肾小球疾病 Fosinopril dosage Proteinuria primary glomerular diseases Clinical trial
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  • 1Levey AS,Coresh J,Balk E,et al.National kidney foundation practice guidelinesfor chronic kidney disease:evaluation,classification,and stratification[J].AnnIntern Med,2003;189(3):137~147.
  • 2Kshirsagar AV,Joy MS,Hogan SL,et al.Effect of ACE inhibitors in diabetic andnondiabetic chronic renal disease:A systematic overview of randomized placebocontrolledtrials[J].Am J Kid Dis,2000;35:695~707.
  • 3黄镇奎.贝那普利联合缬沙坦治疗糖尿病肾病的临床效果观察[J].中国医药导刊,2011,13(6):1036-1037. 被引量:5
  • 4Reddy MS,Landa M,Stark PC,et al.Antiproteinuric dose response of angiotensinconvertingenzyme inhibitors in non-diabetic chronic kidney disease[J].J Am SocNephrol,2002;13(Suppl.S):A264.
  • 5Haas M,Leko-Mohr Z,Erler C,et al.Antiproteinuric versus antihypertensivedrug class on progression of high-dose ACE inhibitor therapy[J].Am J KidneyDis,2002;40:458~463.
  • 6Navis G,Kramer AB,de Jong PE:High-dose ACE inhibition:Can it improverenoprotection[J].Am J Kidney Dis,2002;40:664~666.
  • 7Uechi M,Imamoto,S.Ishikawa Y.Dose-dependent inhibition of angiotensinconverting enzyme by enalapril in cats[J].J Vet Med Sci,2002;64:385~387.
  • 8Izabella Z.A,Pawluczy K,Samita R.The role of bradykinin in theantifibrotic actions of perindoprilat on human mesangial cells[J].KidneyInt,2004;65:1240~1255.
  • 9Donadelli R,Abbate M,Zanchi C,et al.Protein traffic activates NF-kB genesignaling and promotes MCP-1-dependent interstitial inflammation[J].Am JKidney Dis,2000;36:1226~1241.
  • 10Ma L-J,Nakamura S,Whitsitt JS,Marcantoni C,et al.Regression of sclerosisin aging by an angiotensin inhibitioninduced decrease in PAI-1[J].KidneyInt,2000;58:2425~2436.

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