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甲泼尼龙冲击疗法对进行性IgA肾病的影响

[Effects of methylprednisolone pulse therapy on progressive IgA nephropathy].

作者信息

Yoshimura M, Kida H, Saito Y, Takaeda M, Sugioka G

机构信息

Department of Internal Medicine, Kanazawa National Hospital, Japan.

出版信息

Nihon Jinzo Gakkai Shi. 1991 Aug;33(8):761-8.

PMID:1770636
Abstract

In order to estimate the effects of methylprednisolone pulse therapy on progressive IgA nephropathy, clinical parameters in eight patients with the disease were compared between before and after the therapy. In this study progressive IgA nephropathy was defined as follows; 24 hour urinary protein excretion was (++) or more and renal biopsy carried out just before the therapy revealed crescents, inevitably including cellular crescents, in 10% or more glomeruli observed. Methylprednisolone 1000 mg a day was intravenously administered for three consecutive days and the therapy was repeated with an interval of 4 days. The additional third course was given in two patients, in whom significant decrease in urinary protein had not been obtained after the original two courses of the therapy. Oral prednisolone 20 mg a day started simultaneously was tapered one month later to maintenance daily doses of 5-10 mg. After the pulse therapy urinary protein excretion was significantly decreased in every patient with a mean decrease from 2.3 +/- 0.5 (0.8-5.5)g to 1.1 +/- 0.3 (0-2.8)g (p less than 0.05). Glomerular filtration rate (GFR) was increased from 83 +/- 11 (31-115) ml/min to 96 +/- 10 (44-130) ml/min (p less than 0.05). In the initial biopsy crescents were observed in 25 +/- 7 (19-57)% of glomeruli observed and 20-100% of these were composed of cellular crescents. Complete loss of cellular crescents in 6 patients and a marked decrease from 73% to 33% in another were demonstrated by the second biopsies performed after the pulse therapy. These results suggested that the methylprednisolone pulse therapy significantly reduced urinary protein excretion and improved renal function through suppression of new crescent formation as well as transformation of cellular crescents to fibrocellular or fibrous crescents.

摘要

为评估甲泼尼龙冲击疗法对进行性IgA肾病的疗效,比较了8例该疾病患者治疗前后的临床参数。本研究中,进行性IgA肾病定义如下:24小时尿蛋白排泄量为(++)或更高,且治疗前进行的肾活检显示,在所观察的肾小球中,10%或更多出现新月体,不可避免地包括细胞性新月体。每天静脉注射甲泼尼龙1000mg,连续3天,并每隔4天重复该治疗。另外有2例患者接受了第三个疗程的治疗,这2例患者在最初两个疗程治疗后尿蛋白未显著减少。同时开始口服泼尼松龙,每日20mg,1个月后逐渐减量至每日维持剂量5 - 10mg。冲击治疗后,每位患者的尿蛋白排泄量均显著减少,平均从2.3±0.5(0.8 - 5.5)g降至1.1±0.3(0 - 2.8)g(p<0.05)。肾小球滤过率(GFR)从83±11(31 - 115)ml/分钟增至96±10(44 - 130)ml/分钟(p<0.05)。在初次活检中,在所观察的肾小球中,25±7(19 - 57)%出现新月体,其中20% - 100%为细胞性新月体。冲击治疗后进行的第二次活检显示,6例患者的细胞性新月体完全消失,另一例患者的细胞性新月体从73%显著降至33%。这些结果表明,甲泼尼龙冲击疗法通过抑制新新月体形成以及细胞性新月体向纤维细胞性或纤维性新月体的转化,显著降低了尿蛋白排泄量并改善了肾功能。

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