Effects of Antiparkinson Medication on Cognition in Parkinson's Disease: A Systematic Review.

TitleEffects of Antiparkinson Medication on Cognition in Parkinson's Disease: A Systematic Review.
Publication TypeJournal Article
Year of Publication2018
AuteursRoy, M-A, Doiron, M, Talon-Croteau, J, Dupré, N, Simard, M
JournalCan J Neurol Sci
Volume45
Issue4
Pagination375-404
Date Published2018 Jul
ISSN0317-1671
Abstract

OBJECTIVE: This study aimed to systematically review the effects of currently prescribed antiparkinson medication on cognition in patients with mild-to-moderate Parkinson's disease (PD) who were either cognitively intact or mildly impaired.METHODS: English- and French-language studies published between 1969 and 2017 were accessed via MedLine, PsychNET, EMBASE and EBSCO databases. Methodological quality (MQ) was evaluated with the quality assessment instrument of the Cochrane Collaboration Depression, Anxiety and Neurosis Review (scores from 0% to 44% indicate very low quality; scores from 45% to 64% indicate low quality; scores from 65% to 84% indicate medium quality; and scores from 85% to 100% indicate high quality). Hedges' g and Student's t-test were performed on all cognitive outcome measures reported.RESULTS: In total, 14 studies assessed the cognitive effects of levodopa (L-D), pramipexole (PRX), selegiline (SEL) and rasagiline (RAS) in mild-to-moderate non-demented PD patients. The MQ was overall low, with an average score of 49.1%. Results for L-D showed deleterious effects on a test of cognitive inhibition, as well as benefits on tests of attention/processing speed/working memory, executive functions and episodic memory. Pramipexole was associated with a worsening of episodic memory and impulse control. Results on SEL indicated a deterioration of global cognition over time and of concept formation. Rasagiline had some benefits on working memory and verbal fluency.CONCLUSION: Antiparkinson medications can have deleterious (L-D; PRX; SEL) and beneficial (L-D; RAS) effects on cognition. However, randomized double-blind placebo-controlled trials with larger sample sizes are required to better elucidate this issue.

DOI10.1017/cjn.2018.21
Alternate JournalCan J Neurol Sci
PubMed ID29747716