Abstract
BACKGROUND
Levodopa-induced dyskinesias (LID) are amongst the most disabling side-effects of levodopa therapy for Parkinson's disease
(PD). It has been suggested that that N-Methyl-D-Aspartate (NMDA)-receptor antagonist may reduce peak-dose dyskinesia in PD
patients and may lead to motor improvement. In this study, we compared the efficacy of NMDA receptor antagonists versus placebo
in the treatment of LID in PD through a meta-analysis of controlled trials.
METHODS
Electronic search of Pubmed (1990 - 2010), Medline (1966-2010), EMBASE (1974-2010) and other databases for relevant studies
were performed. Controlled clinical trials of the effects of NMDA antagonists on LID that fulfill the study protocol were
selected. Pooled data from included studies was then used to perform random and fixed effect models meta-analysis.
RESULTS
The search resulted in 11 randomized, placebo controlled clinical trials that involved a total of 253 PD patients with peak-dose
LID. The outcome measures were various dyskinesia rating scales and the Unified Parkinson Disease Rating Scale (UPDRS) subscales
III and IV. The analysis showed significant reduction in Standard Mean Difference (SMD) for UPDRS IV (SMD -1.45; 95%CI -2.28
to -0.63) and UPDRS III (SMD -0.41; 95%CI -0.69 to -0.12) after treatment with amantadine. Other included drugs did not show
significant change in the outcomes measured.
CONCLUSION
This meta-analysis provides an update on the clinical trials and confirms the short-term benefits of amantadine therapy in
the treatment of dyskinesia. The effects of other NMDA receptor antagonists need to be evaluated further in clinical trials.
Links
Authors
Institution
Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Source
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 39:4 2012 Jul pg 465-72MeSH
AmantadineDatabases, Factual
Disability Evaluation
Double-Blind Method
Dyskinesia, Drug-Induced
Excitatory Amino Acid Antagonists
Humans
Levodopa
Parkinson Disease
Randomized Controlled Trials as Topic
Receptors, N-Methyl-D-Aspartate
Severity of Illness Index
Pub Type(s)
Journal ArticleMeta-Analysis
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
22728853
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