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慢性炎症性脱髓鞘性多发性神经病对霉酚酸酯治疗有反应。

Chronic inflammatory demyelinating polyneuropathy responsive to mycophenolate mofetil therapy.

机构信息

Department of Neurology, University of Miami, Miller School of Medicine, Miami, FL 33136, USA.

出版信息

J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):634-6. doi: 10.1136/jnnp.2009.177576. Epub 2010 Feb 22.

Abstract

OBJECTIVE

To evaluate the efficacy of mycophenolate mofetil (MMF) in chronic inflammatory demyelinating polyneuropathy (CIDP).

BACKGROUND

Evidence is growing that MMF is effective as an immunomodulatory drug in neuromuscular diseases.

METHODS

A database of 184 patients with CIDP was analysed to obtain clinical, laboratory and electrophysiological information for patients with CIDP treated with MMF.

RESULTS

Eight patients, who met the inclusion criteria, received MMF (mean dose 2 g/day; median duration 15.2 months). The average Neuropathy Impairment Score of the eight patients improved from baseline (72.3+/-35) after initiation of MMF therapy (37.8+/-37; p<0.001). Six of these eight patients were either able to stop concomitant medications (corticosteroid, intravenous immunoglobulin) or reduce their doses and frequency by > or = 50%.

CONCLUSIONS

Our pilot data suggest that MMF appears to be an effective therapy for patients with naive or refractory CIDP, and further controlled studies are warranted for their confirmation.

摘要

目的

评估霉酚酸酯(MMF)在慢性炎症性脱髓鞘性多发性神经病(CIDP)中的疗效。

背景

越来越多的证据表明,MMF 作为一种免疫调节剂在神经肌肉疾病中有效。

方法

对 184 例 CIDP 患者的数据库进行分析,以获得接受 MMF 治疗的 CIDP 患者的临床、实验室和电生理学信息。

结果

符合纳入标准的 8 例患者接受了 MMF(平均剂量 2g/天;中位疗程 15.2 个月)。8 例患者的神经病损伤评分从 MMF 治疗开始时的基线(72.3+/-35)平均改善(37.8+/-37;p<0.001)。这 8 例患者中有 6 例能够停止同时使用的药物(皮质类固醇、静脉注射免疫球蛋白)或减少剂量和频率 >或=50%。

结论

我们的初步数据表明,MMF 似乎对初治或难治性 CIDP 患者有效,需要进一步的对照研究来证实。

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