Zhao M, Chen X, Chen Y, Liu Z, Liu Y, Lu F, Zhang Y, Wang H
Institute of Nephrology, The First Hospital of Peking University, Beijing 100034, China.
Zhonghua Yi Xue Za Zhi. 2001 May 10;81(9):528-31.
To investigate the efficacy and safety of mycophenolate mofetil (MMF) on treating refractory primary nephrotic syndrome.
Forty-one patients with refractory nephrotic syndrome confirmed by renal biopsy, 19 with minor lesion (minimal lesion nephropathy and mesangial proliferative glomerulonephritis), 18 with membranous nephropathy (MN), 3 with focal segmental glomerulosclerosis (FSGS), and one with mesangioproliferative glomerulonephritis (MPGN), were treated by MMF combined with prednisone. The initial dosage of MMF was 1.0 - 2.0 g/d for three months and then the dosage was tapered gradually. The duration of MMF treatment was at least six months. Prednisone at the dose of 20 - 60 g/d was used at the beginning of the combined treatment and then the dosage was tapered gradually. Follow-up interview was conducted regularly. Four patients were rebiopsyed by the end of observation.
The combined treatment of MMF/prednisone decreased the urine protein and elevated the serum albumin significantly among patients with minor lesion and MN (P < 0.001). All patients with minor lesion achieved clinical remission. Eleven of the nineteen cases responded within four weeks, and twelve of them obtained complete clinical remission. The dosage of prednisone could be tapered smoothly among the steroid dependent patients. Thirteen of the eighteen patients with MN achieved remission, however only six responded within four weeks and only three of them achieved complete clinical remission. During the treatment, four patients experienced transient increase of urine protein due to infection and recovered spontaneously without alteration of treatment. Side effects were tolerable except one case was withdrawn due to the decrease of hemoglobin. Renal function remained stable during the treatment. No obvious alteration could be found in renal biopsy by the end of treatment among four patients.
MMF is an effective and safe immunosuppressive agent for refractory nephrotic syndrome.
探讨霉酚酸酯(MMF)治疗难治性原发性肾病综合征的疗效及安全性。
41例经肾活检确诊为难治性肾病综合征的患者,其中19例为轻微病变(微小病变肾病和系膜增生性肾小球肾炎),18例为膜性肾病(MN),3例为局灶节段性肾小球硬化(FSGS),1例为系膜增生性肾小球肾炎(MPGN),采用MMF联合泼尼松治疗。MMF初始剂量为1.0 - 2.0 g/d,持续3个月,然后逐渐减量。MMF治疗时间至少6个月。联合治疗开始时使用剂量为20 - 60 g/d的泼尼松,然后逐渐减量。定期进行随访。观察结束时4例患者再次进行肾活检。
MMF/泼尼松联合治疗使轻微病变和MN患者的尿蛋白明显减少,血清白蛋白显著升高(P < 0.001)。所有轻微病变患者均达到临床缓解。19例中有11例在4周内起效,其中12例获得完全临床缓解。在激素依赖患者中,泼尼松剂量可顺利减量。18例MN患者中有13例缓解,但仅6例在4周内起效,其中仅3例获得完全临床缓解。治疗期间,4例患者因感染出现尿蛋白短暂增加,未经治疗调整自行恢复。除1例因血红蛋白降低而退出治疗外,副作用均可耐受。治疗期间肾功能保持稳定。4例患者治疗结束时肾活检未发现明显改变。
MMF是治疗难治性肾病综合征的一种有效且安全的免疫抑制剂。