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泼尼松治疗特发性膜性肾病患者的一项随机对照试验。

A randomized controlled trial of prednisone in patients with idiopathic membranous nephropathy.

作者信息

Cattran D C, Delmore T, Roscoe J, Cole E, Cardella C, Charron R, Ritchie S

机构信息

Department of Medicine, University of Toronto, ON, Canada.

出版信息

N Engl J Med. 1989 Jan 26;320(4):210-5. doi: 10.1056/NEJM198901263200403.

Abstract

We conducted a prospective randomized study in which patients with biopsy-confirmed idiopathic membranous nephropathy were assigned to receive either a six-month course of prednisone given on alternate days (45 mg per square meter of body-surface area; n = 81) or no specific treatment (n = 77). The mean duration of follow-up was 48 months. Patients in the prednisone group (median age, 46 years) entered with a mean disease duration of 15 months, a median creatinine clearance of 1.2 ml per second per 1.73 m2 (range, 0.25 to 2.6), and a median rate of urinary protein excretion of 6.8 g per day (0.3 to 26). The annual change in the corrected creatinine clearance at six months did not differ between the prednisone group and the control group (0.10 vs. 0.06 ml per second; P = 0.8), or at the last follow-up evaluation (-0.07 vs. -0.02 ml per second; P = 0.2; 95 percent confidence interval on the difference, -0.03 to 0.13). The proportion of patients with complete remission of proteinuria was also similar in the groups at 6 and 12 months and after a mean of 48 months. Outcomes were similar in the two groups with respect to progression to renal failure (3 vs. 4 patients), death (3 vs. 1 patient), complete remission of proteinuria at 36 months (16 vs. 19 patients), and a decline of 25 percent or more in the creatinine clearance at 60 months (32 vs. 25 percent of patients). A multivariate analysis, which adjusted for differences at entry in sex distribution, urinary protein excretion, and creatinine concentration, as well as other prognostic variables, failed to provide an explanation for the lack of effect of prednisone. We conclude that a six-month course of therapy in which prednisone is given on alternate days is of no benefit to patients with idiopathic membranous nephropathy.

摘要

我们进行了一项前瞻性随机研究,将经活检确诊为特发性膜性肾病的患者分为两组,一组接受为期6个月的隔日泼尼松治疗(45mg/每平方米体表面积;n = 81),另一组不接受特定治疗(n = 77)。平均随访时间为48个月。泼尼松组患者(中位年龄46岁)入组时疾病平均病程为15个月,肌酐清除率中位数为每1.73平方米1.2ml/秒(范围0.25至2.6),尿蛋白排泄率中位数为每日6.8g(0.3至26)。泼尼松组和对照组在6个月时校正肌酐清除率的年度变化无差异(0.10对0.06ml/秒;P = 0.8),在最后一次随访评估时也无差异(-0.07对-0.02ml/秒;P = 0.2;差异的95%置信区间为-0.03至0.13)。蛋白尿完全缓解的患者比例在6个月、12个月以及平均48个月后两组也相似。两组在进展至肾衰竭(3例对4例)、死亡(3例对1例)、36个月时蛋白尿完全缓解(16例对19例)以及60个月时肌酐清除率下降25%或更多(32%对25%的患者)方面的结局相似。多变量分析对入组时性别分布、尿蛋白排泄和肌酐浓度的差异以及其他预后变量进行了校正,但未能解释泼尼松无效的原因。我们得出结论,为期6个月的隔日泼尼松治疗对特发性膜性肾病患者无益处。

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