Sheikholeslami Marjan, Hajialilo Mehrzad, Rasi Hashemi Seyed Sadreddin, Malek Mahdavi Aida, Gojazadeh Morteza, Khabbazi Alireza
a Connective Tissue Diseases Research Center , Tabriz University of Medical Sciences , Tabriz , Iran.
b Chronic Renal Failure Research Center , Tabriz University of Medical Sciences , Tabriz , Iran.
Mod Rheumatol. 2018 May;28(3):523-529. doi: 10.1080/14397595.2017.1352479. Epub 2017 Jul 28.
This study aimed to evaluate long-term efficacy of low dose cyclosporine A (CsA) in the treatment of resistant proliferative lupus nephritis.
In this retrospective study, patients with biopsy proven proliferative lupus nephritis who were unresponsive to combination therapy with steroid plus mycophenolate mofetil (MMF) or cyclophosphamide (CYC) and had been treated with CsA were included. Efficacy monitoring was based on the systemic lupus erythematosus (SLE) disease activity index, dose of prednisolone, serum complement, anti-double stranded DNA (anti-dsDNA) titration, urine analysis, proteinuria, creatinine clearance, remission of the renal disease, renal survival and involvement of other organs.
This study included 27 consecutive patients (22 females, 5 males) with resistant proliferative lupus nephritis. Mean duration of follow up and treatment with CsA were 40.7 ± 24.9 and 35.2 ± 19.1 months, respectively. Complete and partial renal remission occurred in 66.9% and 25.7% patients, respectively. Creatinine clearance was stable, proteinuria and anti-dsDNA titer decreased, and C3 and C4 increased significantly during the treatment with CsA. Severe complications such as death, dialysis, kidney transplantation and severe infection did not occur in the studied patients during the follow-up period.
Low-dose CsA could induce renal remission and ameliorate the SLE disease activity in patients with resistant proliferative lupus nephritis and it would be a safe drug for treatment of these patients.
本研究旨在评估低剂量环孢素A(CsA)治疗难治性增殖性狼疮性肾炎的长期疗效。
在这项回顾性研究中,纳入了经活检证实为增殖性狼疮性肾炎、对类固醇联合霉酚酸酯(MMF)或环磷酰胺(CYC)联合治疗无反应且接受过CsA治疗的患者。疗效监测基于系统性红斑狼疮(SLE)疾病活动指数、泼尼松龙剂量、血清补体、抗双链DNA(抗dsDNA)滴定、尿液分析、蛋白尿、肌酐清除率、肾病缓解情况、肾脏存活率以及其他器官受累情况。
本研究纳入了27例连续性难治性增殖性狼疮性肾炎患者(22例女性,5例男性)。CsA的平均随访时间和治疗时间分别为40.7±24.9个月和35.2±19.1个月。分别有66.9%和25.7%的患者实现了完全和部分肾脏缓解。在CsA治疗期间,肌酐清除率稳定,蛋白尿和抗dsDNA滴度降低,C3和C4显著升高。在随访期间,研究患者未发生死亡、透析、肾移植和严重感染等严重并发症。
低剂量CsA可诱导难治性增殖性狼疮性肾炎患者的肾脏缓解并改善SLE疾病活动,且对这些患者来说是一种安全的治疗药物。