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脉冲环磷酰胺治疗增殖性狼疮性肾炎的疗效

The outcome of proliferative lupus nephritis with pulse cyclophosphamide therapy.

作者信息

Annavarajula S K, Murty K V D, Prayaga A, Das U, Desai M, Narain C A

机构信息

Department of Nephrology, Nizam's Institute of Medical Sciences, Hyderabad, India.

出版信息

Indian J Nephrol. 2011 Jul;21(3):160-5. doi: 10.4103/0971-4065.83933.

Abstract

Proliferative lupus nephritis deserves aggressive therapy and cyclophosphamide plays a pivotal role. Thirty nine patients with proliferative lupus nephritis (Class III-7 patients and Class IV- 32 patients) with a median follow up of 38 months were considered for this observational study. All the patients received induction therapy with intravenous methylprednisolone. Cyclophosphamide was given intravenously initially in monthly pulses for six months and later quarterly pulses until remission was achieved or until the target dose (200 mg/kg) was reached. The treatment with intravenous methylprednisolone was repeated in the event of a nephritic flare. Later the corticosteroid was reduced to a minimum effective dose and cyclophosphamide was changed to either azathioprine or mycophenolate mofetil. At the time of the last follow up, 82.05% of the patients were in remission (complete remission 51.28% and partial remission 30.77%). The median interval to achieve remission in responders was 15 months. Early diagnosis (P=0.04), a higher creatinine clearance at presentation (P=0.02), and concurrent use of an ACEI or an ARB (P=007) significantly favored attaining remission. Five patients experienced a doubling of serum creatinine and one of them became dialysis dependent. Risk of doubling of serum creatinine correlated with a low Ccr (P=0.03) at presentation, occurrence of renal flares (P=0.034) and failure to achieve remission (P=0.0001). The parameters like serum creatinine, serum C3, serum C4, activity and chronicity indices on renal biopsy, hypertension were not statistically significant. Therapy with cyclophosphamide, if initiated early, helps in inducing remission and hence can retard the progression to CKD.

摘要

增殖性狼疮性肾炎需要积极治疗,环磷酰胺起着关键作用。本观察性研究纳入了39例增殖性狼疮性肾炎患者(Ⅲ级7例,Ⅳ级32例),中位随访时间为38个月。所有患者均接受静脉注射甲泼尼龙诱导治疗。环磷酰胺最初每月静脉脉冲给药一次,共6个月,之后每季度脉冲给药一次,直至缓解或达到目标剂量(200mg/kg)。若出现肾炎发作,则重复静脉注射甲泼尼龙治疗。随后将皮质类固醇减至最低有效剂量,并将环磷酰胺换用硫唑嘌呤或霉酚酸酯。在最后一次随访时,82.05%的患者病情缓解(完全缓解51.28%,部分缓解30.77%)。缓解者达到缓解的中位时间为15个月。早期诊断(P=0.04)、就诊时较高的肌酐清除率(P=0.02)以及同时使用血管紧张素转换酶抑制剂(ACEI)或血管紧张素Ⅱ受体阻滞剂(ARB)(P=0.07)显著有利于病情缓解。5例患者血清肌酐翻倍,其中1例依赖透析。血清肌酐翻倍的风险与就诊时低Ccr(P=0.03)、肾发作的发生(P=0.034)以及未达到缓解(P=0.0001)相关。血清肌酐、血清C3、血清C4、肾活检的活动度和慢性指数、高血压等参数无统计学意义。早期开始使用环磷酰胺治疗有助于诱导缓解,从而可延缓向慢性肾脏病的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40e3/3161432/b31acdf85f6a/IJN-21-160-g002.jpg

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