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Randomized clinical trial of topiramate for levodopa-induced dyskinesia in Parkinson's disease.
Kobylecki, Christopher; Burn, David J; Kass-Iliyya, Lewis; Kellett, Mark W; Crossman, Alan R; Silverdale, Monty A.
Afiliação
  • Kobylecki C; Centre for Clinical and Cognitive Neurosciences, Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK; Department of Neurology, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Salford, UK. Electronic address: christopher.kobylecki@man
  • Burn DJ; Institute for Ageing and Health, Newcastle University, Newcastle, UK.
  • Kass-Iliyya L; Centre for Clinical and Cognitive Neurosciences, Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK; Department of Neurology, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Salford, UK.
  • Kellett MW; Department of Neurology, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Salford, UK.
  • Crossman AR; Faculty of Life Sciences, University of Manchester, Manchester, UK.
  • Silverdale MA; Centre for Clinical and Cognitive Neurosciences, Institute of Brain, Behaviour and Mental Health, University of Manchester, Manchester, UK; Department of Neurology, Greater Manchester Neurosciences Centre, Salford Royal NHS Foundation Trust, Salford, UK.
Parkinsonism Relat Disord ; 20(4): 452-5, 2014 Apr.
Article em En | MEDLINE | ID: mdl-24521874
ABSTRACT

BACKGROUND:

The antiepileptic drug topiramate reduces levodopa-induced dyskinesia without exacerbating parkinsonism in animal models. We report a randomized, double-blind, placebo-controlled crossover trial in patients with Parkinson's disease and levodopa-induced dyskinesia.

METHODS:

Fifteen patients with Parkinson's disease and stable levodopa-induced dyskinesia were enrolled into the study, of whom 13 were randomized to topiramate or placebo. The study medication was titrated to 100 mg/day over four weeks, and assessments were carried out after a further two weeks. Dyskinesia severity assessed by a blinded rater from video recordings was the primary outcome measure.

RESULTS:

Seven patients (mean age 58.9 ± 12.8 years) completed the study. Patients taking topiramate vs. placebo showed a significant increase in dyskinesia severity compared to baseline (Wilcoxon signed rank test, P = 0.043). Five patients withdrew from the study whilst taking topiramate due to adverse effects.

CONCLUSIONS:

Topiramate tended to worsen dyskinesia in patients with Parkinson's disease, and was poorly tolerated.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Discinesia Induzida por Medicamentos / Frutose / Anticonvulsivantes Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Parkinson / Discinesia Induzida por Medicamentos / Frutose / Anticonvulsivantes Idioma: En Ano de publicação: 2014 Tipo de documento: Article