Department of Nephrology, Tianjin First Central Hospital, No.24 Fukang Road, Tianjin, 300192, China.
Int Urol Nephrol. 2021 Apr;53(4):725-731. doi: 10.1007/s11255-020-02680-y. Epub 2020 Nov 6.
Membraneous nephropathy (MN) is one of the complicated kidney diseases associated with proteinuria. Mizoribine (MZR) is an emerging treatment option for nephrotic syndrome; however, its dosage and administration are yet lack of consensus. This study aims to evaluate the efficacy and safety of high-dose MZR pulse therapy for adult membraneous nephropathy. Sixty patients with membraneous nephropathy were recruited, and assigned to two treatment groups. One group received conventional treatment of steroid combining with cyclophosphamide (CPM), the other group received steroid combining with high-dose MZR pulse administration. Both groups were followed up for 1 year. Treatment efficacy and side effects were measured regularly. Fifty-nine patients completed the treatment courses. There was no significant difference in demographic and disease conditions prior to treatment between two treatment groups. Both groups showed significant decrease of urine proteins and increase of serum albumin levels after treatments with no severe side effects. After 6 months of treatment, MZR group has 71% reduction (compared to 74.4% reduction in CPM group) in urine protein compared to baseline after adjusting for age and gender. 89.7% of patients in CPM and 93.3% in MZR groups had partial/ complete remission after 12 months. This study demonstrated satisfactory safety and efficacy of high-dose mizoribine pulse administration combining with steroid treatment for adult patients with membranous nephropathy.
膜性肾病(MN)是一种与蛋白尿相关的复杂肾脏疾病。吗替麦考酚酯(MZR)是治疗肾病综合征的新兴治疗选择;然而,其剂量和给药方案仍缺乏共识。本研究旨在评估大剂量 MZR 脉冲疗法治疗成人膜性肾病的疗效和安全性。
招募了 60 名膜性肾病患者,并将其分为两组。一组接受常规治疗,即激素联合环磷酰胺(CPM),另一组接受激素联合大剂量 MZR 脉冲治疗。两组均随访 1 年。定期测量治疗效果和副作用。
59 名患者完成了治疗过程。在治疗前,两组患者的人口统计学和疾病状况无显著差异。两组患者在治疗后尿蛋白显著减少,血清白蛋白水平显著增加,且无严重副作用。治疗 6 个月后,MZR 组的尿蛋白与基线相比,经年龄和性别调整后,减少了 71%(CPM 组减少了 74.4%)。CPM 组和 MZR 组分别有 89.7%和 93.3%的患者在 12 个月时部分/完全缓解。
本研究表明,大剂量吗替麦考酚酯脉冲联合激素治疗成人膜性肾病具有良好的安全性和疗效。