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 ≥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.
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Presented as an abstract at the 61st AAN meeting, 25 April to 2 May, 2009, Seattle, Washington, USA.
Competing interests None.
Ethics approval This study was conducted with the approval of the Institutional Review Board, University of Miami Miller School of Medicine, Miami, Florida, USA.
Provenance and peer review Not commissioned; externally peer reviewed.
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