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Rivastigmine in apathetic but dementia and depression-free patients with Parkinson's disease: a double-blind, placebo-controlled, randomised clinical trial

2013; BMJ; Volume: 85; Issue: 6 Linguagem: Inglês

10.1136/jnnp-2013-306439

1468-330X

David Devos, Caroline Moreau, David Maltête, Romain Lefaucheur, Alexandre Kreisler, Alexandre Eusébio, Gilles Defer, Thavarak Ouk, J.-P. Azulay, Pierre Krystkowiak, Tatiana Witjas, Marie Delliaux, A. Destée, Alain Duhamel, Régis Bordet, Luc Defebvre, Kathy Dujardin,

Alzheimer's disease research and treatments

Background Even with optimal dopaminergic treatments, many patients with Parkinson9s disease (PD) are frequently incapacitated by apathy prior to the development of dementia. We sought to establish whether rivastigmine9s ability to inhibit acetyl- and butyrylcholinesterases could relieve the symptoms of apathy in dementia-free, non-depressed patients with advanced PD. Methods We performed a multicentre, parallel, double-blind, placebo-controlled, randomised clinical trial (Protocol ID: 2008-002578-36; clinicaltrials.gov reference: NCT00767091) in patients with PD with moderate to severe apathy (despite optimised dopaminergic treatment) and without dementia. Patients from five French university hospitals were randomly assigned 1:1 to rivastigmine (transdermal patch of 9.5 mg/day) or placebo for 6 months. The primary efficacy criterion was the change over time in the Lille Apathy Rating Scale (LARS) score. Finding 101 consecutive patients were screened, 31 were eligible and 16 and 14 participants were randomised into the rivastigmine and placebo groups, respectively. Compared with placebo, rivastigmine improved the LARS score (from −11.5 (−15/−7) at baseline to −20 (−25/−12) after treatment; F (1, 25) =5.2; p=0.031; adjusted size effect: −0.9). Rivastigmine also improved the caregiver burden and instrumental activities of daily living but failed to improve quality of life. No severe adverse events occurred in the rivastigmine group. Interpretation Rivastigmine may represent a new therapeutic option for moderate to severe apathy in advanced PD patients with optimised dopaminergic treatment and without depression dementia. These findings require confirmation in a larger clinical trial. Our results also confirmed that the presence of apathy can herald a pre-dementia state in PD. Registration Clinicaltrials.gov reference: NCT00767091.