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2-巯基丙酰甘氨酸(2-MPG)诱导的膜性肾小球肾炎

Membranous glomerulonephritis induced by 2-mercaptopropionylglycine (2-MPG).

作者信息

Lindell A, Denneberg T, Eneström S, Fich C, Skogh T

机构信息

Department of Nephrology, Faculty of Health Sciences, University of Linköping, Sweden.

出版信息

Clin Nephrol. 1990 Sep;34(3):108-15.

PMID:2225561
Abstract

Thirty-two patients suffering from cystinuria were treated with 2-mercaptopropionylglycine (2-MPG) for 0.5-10 years (average 6.3 years). After 4-14 months of treatment at daily doses ranging from 500 to 2500 mg, three patients developed slight to moderate proteinuria. Two patients were subjected to renal biopsy which showed membranous glomerulonephritis. In one biopsy signs of progressive glomerular lesions were observed. In seven patients (22%) antinuclear antibodies were demonstrated. In one patient with biopsy-proven membranous glomerulonephritis, the antinuclear antibodies consisted of antihistone antibodies. The observations presented in this report indicate that 2-MPG, like D-penicillamine, could induce autoimmune reactions, in some cases leading to membranous glomerulonephritis. The prognosis seemed to be favorable. However, the occurrence of irreversible glomerular lesions as reported by us should be borne in mind when considering long-term treatment with 2-MPG. A continuous, close follow-up of patients on 2-MPG treatment is recommended.

摘要

32例胱氨酸尿症患者接受2-巯基丙酰甘氨酸(2-MPG)治疗0.5至10年(平均6.3年)。在每日剂量为500至2500毫克的治疗4至14个月后,3例患者出现轻度至中度蛋白尿。2例患者接受了肾活检,结果显示为膜性肾小球肾炎。在一次活检中观察到了进行性肾小球病变的迹象。7例患者(22%)检测出抗核抗体。在1例经活检证实为膜性肾小球肾炎的患者中,抗核抗体由抗组蛋白抗体组成。本报告中的观察结果表明,2-MPG与D-青霉胺一样,可能诱发自身免疫反应,在某些情况下导致膜性肾小球肾炎。预后似乎良好。然而,在考虑用2-MPG进行长期治疗时,应牢记我们所报告的不可逆肾小球病变的发生情况。建议对接受2-MPG治疗的患者进行持续、密切的随访。

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