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环孢素A联合中/低剂量泼尼松治疗进展性IgA肾病观察
Research of Cyclosporine A Combined with Union/Low dose Prednisone on the Treatment of Progressive IgA Nephropathy
  
DOI:
中文关键词:  环孢素A  泼尼松  进展性IgA肾病  临床疗效
英文关键词:Cyclosporin A  Prednisone  Progressive IgA nephropathy  Clinical efficacy
基金项目:2012年浙江省丽水市科技项目(编号:2012ZC041)
作者单位
王晓文 王岸文 张全全 桂志红 王华富 ①蕲春县人民医院肾内科(湖北黄冈 435300)②浙江省丽水市人民医院肾内科。 
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中文摘要:
      摘 要 目的:探讨环孢素A联合中/低剂量泼尼松治疗进展性IgA肾病的临床疗效和安全性。方法:进展性IgA肾病患者120例随机分为观察组和对照组每组60例。对照组晨起顿服大剂量泼尼松,起始剂量1.0 mg·kg-1·d-1,最大量60 mg·d-1,6周后(或尿蛋白转阴后2周)逐渐减量,至12周时减至0.5 mg·kg-1·d-1,维持治疗;观察组给予环孢素A+泼尼松治疗,环孢素A起始剂量100 mg·d-1,根据血药浓度调整用量,最大不超过5.0 mg·kg-1·d-1, 使环孢素 A 谷浓度维持在100~200 mg·ml-1;波尼松起始剂量0.5 mg·kg-1·d-1,最大量30 mg·d-1。两组均治疗6个月以上。分别于治疗2,4,6,8,12,24周观察两组患者24 h 尿蛋白、血白蛋白、肌酐、尿酸等指标变化,评价两组的临床疗效和药品不良反应。结果:观察组治疗4,8,12,24周时的总缓解率均显著高于对照组(P<0.05)。治疗2,4,8,12,24周时,两组24 h 尿蛋白均显著下降(P<0.05),且观察组明显低于对照组(P<0.05)。观察组治疗4,8,12,24周时血白蛋白较治疗前显著上升(P<0.05),且显著高于对照组同期(P<0.05);而对照组治疗期间血白蛋白无明显变化(P>0.05)。治疗前后两组患者血肌酐和尿酸水平比较,差异无统计学意义(P>0.05)。两组药品不良反应发生率比较,差异无统计学意义(P>0.05)。结论:环孢素A联合中/低剂量泼尼松治疗进展性IgA肾病临床疗效好,安全性高,值得临床推广。
英文摘要:
      ABSTRACT Objective:To discuss the curative effects and clinical safety of cyclosporine A combined with union/low dose prednisone on the treatment of progressive IgA nephropathy.Methods:120 cases of progressive IgA nephropathy patients were randomly divided into observation group and control group (60 cases in each group). The control group were given large doses of prednisone and a starting dose of 1.0mg·kg-1·d-1, with the maximum amount of 60mg·d-1; And after 6 weeks of (or urine protein was negative after two weeks) tapering, when reduced to 12 weeks 0.5 mg·kg-1·d-1, all patients were given maintenance treatment. The observation group received cyclosporine A with a starting dose of 100 mg·d-1, and adjusted according to the amount of cyclosporine A, with the maximum not exceeding 5.0 mg·kg-1·d-1, so that concentration of cyclosporin A was maintained at 100 200 mg·ml-1, besides prednisone with a starting dose of 0.5mg· kg-1·d-1, with the maximum amount of 30mg·d-1, which were treated for 6 months. 2 ,4,6,8,12 and 24 weeks after treatment,24 h urinary protein, serum albumin, creatinine, uric acid, and the clinical efficacy and adverse reactions of the two groups were evaluated and compared. Results: In the observation group,4 , 8, 12 and 24 weeks after treatment,the overall response rate was significantly higher than that in the control group (P <0.05). 2 , 4 , 8 , 12 and 24 weeks after treatment in the two groups,24 h urinary protein was all decreased significantly (P<0.05), while observation group was decreased more significantly than control group at the same time( P<0.05). In 4 , 8, 12 and 24 weeks after treatment, serum albumin of observation group was significantly increased than before treatment (P<0.05), and was much higher than control group (P<0.05). There was no significant change on serum albumin of control group during treatment.There were no statistically significant differences on creatinine and uric acid between the two groups before and after treatment (P>0.05). There also has no statistically significant differences on the incidence of adverse reactions between the two groups(P>0.05). Conclusion:Using cyclosporine A combined with union/low dose prednisone to treat progressive IgA nephropathy has better clinical efficacy and higher clinical safety, worthy of promotion.
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