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Effects of Antiparkinson Medication on Cognition in Parkinson’s Disease: A Systematic Review
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 bet...
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Published in: | Canadian journal of neurological sciences 2018-07, Vol.45 (4), p.375-404 |
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description | 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. Objectif: Cette étude vise à recenser systématiquement les effets cognitifs de certains antiparkinsoniens chez des patients aux stades léger à modéré de maladie de Parkinson (MP) avec ou sans atteintes cognitives légères. Méthode: Les publications anglophones et francophones de 1969 à 2017 ont été recensées via MedLine, PsychNET, EMBASE et EBSCO. La qualité méthodologique (QM) a été évaluée avec un instrument de la Cochrane Collaboration Depression, Anxiety and Neurosis Review (0% à 44% signifie une très faible qualité; 45% à 64% une faible qualité; 65% à 84% une qualité moyenne; 85% à 100% une haute qualité). Le g de Hedges et le t de Student ont été calculés pour tous les résultats cognitifs. Résultats: Quatorze études évaluaient les e |
doi_str_mv | 10.1017/cjn.2018.21 |
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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. Objectif: Cette étude vise à recenser systématiquement les effets cognitifs de certains antiparkinsoniens chez des patients aux stades léger à modéré de maladie de Parkinson (MP) avec ou sans atteintes cognitives légères. Méthode: Les publications anglophones et francophones de 1969 à 2017 ont été recensées via MedLine, PsychNET, EMBASE et EBSCO. La qualité méthodologique (QM) a été évaluée avec un instrument de la Cochrane Collaboration Depression, Anxiety and Neurosis Review (0% à 44% signifie une très faible qualité; 45% à 64% une faible qualité; 65% à 84% une qualité moyenne; 85% à 100% une haute qualité). Le g de Hedges et le t de Student ont été calculés pour tous les résultats cognitifs. Résultats: Quatorze études évaluaient les effets cognitifs de levodopa, pramipexole, selegiline et rasagiline chez des patients aux stades léger à modéré de MP sans démence. Globalement, la QM était faible (moyenne de 49.1%). Levodopa est associé à une altération des capacités d’inhibition et des bénéfices aux tests d’attention/vitesse de traitement/mémoire de travail, de fonctions exécutives et de mémoire épisodique. Pramipexole est associé à une détérioration en mémoire épisodique et en contrôle des impulsions. Selegiline est associé à une détérioration de la cognition globale et de la formation de concepts. Rasagiline est associé à des bénéfices en mémoire de travail et en fluidité verbale. Conclusion: Les antiparkinsoniens peuvent avoir des effets cognitifs délétères (levodopa; pramipexole; selegiline) et bénéfiques (rasagiline; levodopa). Davantage d’essais randomisés en double-aveugle et contrôle placebo sont nécessaires pour détailler ces effets.</description><identifier>ISSN: 0317-1671</identifier><identifier>EISSN: 2057-0155</identifier><identifier>DOI: 10.1017/cjn.2018.21</identifier><identifier>PMID: 29747716</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><subject>Antiparkinson Agents - therapeutic use ; Attention ; Brain damage ; Cognition & reasoning ; Cognition Disorders - drug therapy ; Cognition Disorders - etiology ; Cognitive ability ; Dopamine ; Double-blind studies ; Executive function ; Genes ; Humans ; Memory ; Neuropsychology ; Original Article ; Parkinson Disease - complications ; Parkinson Disease - drug therapy ; Parkinson's disease ; Systematic review</subject><ispartof>Canadian journal of neurological sciences, 2018-07, Vol.45 (4), p.375-404</ispartof><rights>Copyright © 2018 The Canadian Journal of Neurological Sciences Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-a67bd3aaed80ec483f282868ccf626a7806ce4ab1addd527d84f0a038de6b08d3</citedby><cites>FETCH-LOGICAL-c392t-a67bd3aaed80ec483f282868ccf626a7806ce4ab1addd527d84f0a038de6b08d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0317167118000215/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,72960</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29747716$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roy, Marc-André</creatorcontrib><creatorcontrib>Doiron, Maxime</creatorcontrib><creatorcontrib>Talon-Croteau, Jessica</creatorcontrib><creatorcontrib>Dupré, Nicolas</creatorcontrib><creatorcontrib>Simard, Martine</creatorcontrib><title>Effects of Antiparkinson Medication on Cognition in Parkinson’s Disease: A Systematic Review</title><title>Canadian journal of neurological sciences</title><addtitle>Can. J. Neurol. Sci</addtitle><description>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. Objectif: Cette étude vise à recenser systématiquement les effets cognitifs de certains antiparkinsoniens chez des patients aux stades léger à modéré de maladie de Parkinson (MP) avec ou sans atteintes cognitives légères. Méthode: Les publications anglophones et francophones de 1969 à 2017 ont été recensées via MedLine, PsychNET, EMBASE et EBSCO. La qualité méthodologique (QM) a été évaluée avec un instrument de la Cochrane Collaboration Depression, Anxiety and Neurosis Review (0% à 44% signifie une très faible qualité; 45% à 64% une faible qualité; 65% à 84% une qualité moyenne; 85% à 100% une haute qualité). Le g de Hedges et le t de Student ont été calculés pour tous les résultats cognitifs. Résultats: Quatorze études évaluaient les effets cognitifs de levodopa, pramipexole, selegiline et rasagiline chez des patients aux stades léger à modéré de MP sans démence. Globalement, la QM était faible (moyenne de 49.1%). Levodopa est associé à une altération des capacités d’inhibition et des bénéfices aux tests d’attention/vitesse de traitement/mémoire de travail, de fonctions exécutives et de mémoire épisodique. Pramipexole est associé à une détérioration en mémoire épisodique et en contrôle des impulsions. Selegiline est associé à une détérioration de la cognition globale et de la formation de concepts. Rasagiline est associé à des bénéfices en mémoire de travail et en fluidité verbale. Conclusion: Les antiparkinsoniens peuvent avoir des effets cognitifs délétères (levodopa; pramipexole; selegiline) et bénéfiques (rasagiline; levodopa). Davantage d’essais randomisés en double-aveugle et contrôle placebo sont nécessaires pour détailler ces effets.</description><subject>Antiparkinson Agents - therapeutic use</subject><subject>Attention</subject><subject>Brain damage</subject><subject>Cognition & reasoning</subject><subject>Cognition Disorders - drug therapy</subject><subject>Cognition Disorders - etiology</subject><subject>Cognitive ability</subject><subject>Dopamine</subject><subject>Double-blind studies</subject><subject>Executive function</subject><subject>Genes</subject><subject>Humans</subject><subject>Memory</subject><subject>Neuropsychology</subject><subject>Original Article</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson's disease</subject><subject>Systematic review</subject><issn>0317-1671</issn><issn>2057-0155</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpt0N1KwzAYBuAgipvTI8-l4IkgnUnaJqlnY84fmCj-nBrS5OvIXNvZdMrOvA1vzysxc5uCCIEk8OT9wovQPsFdggk_0eOySzERXUo2UJvihIeYJMkmauOI8JAwTlpox7kxxpQlLN5GLZrymHPC2uhpkOegGxdUedArGztV9bMtXVUG12CsVo31R7_61ai03xdbBrdr9Pn-4YIz60A5OA16wf3cNVD4Rzq4g1cLb7toK1cTB3urvYMezwcP_ctweHNx1e8NQx2ltAkV45mJlAIjMOhYRDkVVDChdc4oU1xgpiFWGVHGmIRyI-IcKxwJAyzDwkQddLTMndbVywxcIwvrNEwmqoRq5iT1ljKWYuHp4R86rmZ16X8nKU9TEdOEY6-Ol0rXlXM15HJa20LVc0mwXNQufe1yUbukxOuDVeYsK8D82HXPHoSrOFVktTUj-J36X-AX6fWNng</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>Roy, Marc-André</creator><creator>Doiron, Maxime</creator><creator>Talon-Croteau, Jessica</creator><creator>Dupré, Nicolas</creator><creator>Simard, Martine</creator><general>Cambridge University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>M0S</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201807</creationdate><title>Effects of Antiparkinson Medication on Cognition in Parkinson’s Disease: A Systematic Review</title><author>Roy, Marc-André ; Doiron, Maxime ; Talon-Croteau, Jessica ; Dupré, Nicolas ; Simard, Martine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-a67bd3aaed80ec483f282868ccf626a7806ce4ab1addd527d84f0a038de6b08d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antiparkinson Agents - therapeutic use</topic><topic>Attention</topic><topic>Brain damage</topic><topic>Cognition & reasoning</topic><topic>Cognition Disorders - drug therapy</topic><topic>Cognition Disorders - etiology</topic><topic>Cognitive ability</topic><topic>Dopamine</topic><topic>Double-blind studies</topic><topic>Executive function</topic><topic>Genes</topic><topic>Humans</topic><topic>Memory</topic><topic>Neuropsychology</topic><topic>Original Article</topic><topic>Parkinson Disease - complications</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson's disease</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roy, Marc-André</creatorcontrib><creatorcontrib>Doiron, Maxime</creatorcontrib><creatorcontrib>Talon-Croteau, Jessica</creatorcontrib><creatorcontrib>Dupré, Nicolas</creatorcontrib><creatorcontrib>Simard, Martine</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Psychology Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Canadian journal of neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roy, Marc-André</au><au>Doiron, Maxime</au><au>Talon-Croteau, Jessica</au><au>Dupré, Nicolas</au><au>Simard, Martine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Antiparkinson Medication on Cognition in Parkinson’s Disease: A Systematic Review</atitle><jtitle>Canadian journal of neurological sciences</jtitle><addtitle>Can. J. Neurol. Sci</addtitle><date>2018-07</date><risdate>2018</risdate><volume>45</volume><issue>4</issue><spage>375</spage><epage>404</epage><pages>375-404</pages><issn>0317-1671</issn><eissn>2057-0155</eissn><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. Objectif: Cette étude vise à recenser systématiquement les effets cognitifs de certains antiparkinsoniens chez des patients aux stades léger à modéré de maladie de Parkinson (MP) avec ou sans atteintes cognitives légères. Méthode: Les publications anglophones et francophones de 1969 à 2017 ont été recensées via MedLine, PsychNET, EMBASE et EBSCO. La qualité méthodologique (QM) a été évaluée avec un instrument de la Cochrane Collaboration Depression, Anxiety and Neurosis Review (0% à 44% signifie une très faible qualité; 45% à 64% une faible qualité; 65% à 84% une qualité moyenne; 85% à 100% une haute qualité). Le g de Hedges et le t de Student ont été calculés pour tous les résultats cognitifs. Résultats: Quatorze études évaluaient les effets cognitifs de levodopa, pramipexole, selegiline et rasagiline chez des patients aux stades léger à modéré de MP sans démence. Globalement, la QM était faible (moyenne de 49.1%). Levodopa est associé à une altération des capacités d’inhibition et des bénéfices aux tests d’attention/vitesse de traitement/mémoire de travail, de fonctions exécutives et de mémoire épisodique. Pramipexole est associé à une détérioration en mémoire épisodique et en contrôle des impulsions. Selegiline est associé à une détérioration de la cognition globale et de la formation de concepts. Rasagiline est associé à des bénéfices en mémoire de travail et en fluidité verbale. Conclusion: Les antiparkinsoniens peuvent avoir des effets cognitifs délétères (levodopa; pramipexole; selegiline) et bénéfiques (rasagiline; levodopa). Davantage d’essais randomisés en double-aveugle et contrôle placebo sont nécessaires pour détailler ces effets.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><pmid>29747716</pmid><doi>10.1017/cjn.2018.21</doi><tpages>30</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antiparkinson Agents - therapeutic use Attention Brain damage Cognition & reasoning Cognition Disorders - drug therapy Cognition Disorders - etiology Cognitive ability Dopamine Double-blind studies Executive function Genes Humans Memory Neuropsychology Original Article Parkinson Disease - complications Parkinson Disease - drug therapy Parkinson's disease Systematic review |
title | Effects of Antiparkinson Medication on Cognition in Parkinson’s Disease: A Systematic Review |
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