REM sleep behavior disorder, hallucinations, and cognitive impairment in Parkinson's disease
Identifieur interne : 002D42 ( Istex/Corpus ); précédent : 002D41; suivant : 002D43REM sleep behavior disorder, hallucinations, and cognitive impairment in Parkinson's disease
Auteurs : Elena Sinforiani ; Roberta Zangaglia ; Raffaele Manni ; Silvano Cristina ; Enrico Marchioni ; Giuseppe Nappi ; Francesca Mancini ; Claudio PacchettiSource :
- Movement Disorders [ 0885-3185 ] ; 2006-04.
English descriptors
Abstract
The objective of this study was to evaluate the relationship between REM sleep behavior disorder (RBD), hallucinations, and cognitive impairment in Parkinson's disease (PD). One hundred and ten PD patients, divided into three groups (without RBD or hallucinations; with RBD but no hallucinations; with RBD and hallucinations), were submitted to neuropsychological evaluation. The group without RBD and hallucinations showed normal neuropsychological tests when compared to normal controls. The group with hallucinations was characterized by a more severe cognitive impairment affecting both short‐ and long‐term memory, logical abilities, and frontal functions, while the RBD‐only group presented frontal impairment. The hypothesis that RBD in PD can be considered a risk factor not only of the hallucinations but also of more severe and diffuse cognitive abnormalities needs to be strengthened through a longitudinal evaluation. © 2005 Movement Disorder Society
Url:
DOI: 10.1002/mds.20719
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ISTEX:0C1D10FDC9669F1C3E8E0E8E1FEB144BEB2FDB66Le document en format XML
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The group without RBD and hallucinations showed normal neuropsychological tests when compared to normal controls. The group with hallucinations was characterized by a more severe cognitive impairment affecting both short‐ and long‐term memory, logical abilities, and frontal functions, while the RBD‐only group presented frontal impairment. 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Mondino Institute of Neurology, Pavia, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af2" countryCode="IT" type="organization"><unparsedAffiliation>Parkinson's Disease and Movement Disorders Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af3" countryCode="IT" type="organization"><unparsedAffiliation>Sleep Medicine Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af4" countryCode="IT" type="organization"><unparsedAffiliation>Laboratory of Epidemiology and Statistics, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af5" countryCode="IT" type="organization"><unparsedAffiliation>Department of Neurology and Otolaryngology, University La Sapienza, Rome, Italy</unparsedAffiliation></affiliation><affiliation xml:id="af6" countryCode="IT" type="organization"><unparsedAffiliation>IRCCS C. Mondino Institute of Neurology, Pavia, Italy</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en" type="author"><keyword xml:id="kwd1">Parkinson's disease</keyword><keyword xml:id="kwd2">REM sleep behavior disorder</keyword><keyword xml:id="kwd3">hallucinations</keyword><keyword xml:id="kwd4">cognitive impairment</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p>The objective of this study was to evaluate the relationship between REM sleep behavior disorder (RBD), hallucinations, and cognitive impairment in Parkinson's disease (PD). One hundred and ten PD patients, divided into three groups (without RBD or hallucinations; with RBD but no hallucinations; with RBD and hallucinations), were submitted to neuropsychological evaluation. The group without RBD and hallucinations showed normal neuropsychological tests when compared to normal controls. The group with hallucinations was characterized by a more severe cognitive impairment affecting both short‐ and long‐term memory, logical abilities, and frontal functions, while the RBD‐only group presented frontal impairment. The hypothesis that RBD in PD can be considered a risk factor not only of the hallucinations but also of more severe and diffuse cognitive abnormalities needs to be strengthened through a longitudinal evaluation. © 2005 Movement Disorder Society</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><!--Version 0.6 générée le 3-12-2015--><mods version="3.6"><titleInfo lang="en"><title>REM sleep behavior disorder, hallucinations, and cognitive impairment in Parkinson's disease</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>REM Sleep Behavior Disorder</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>REM sleep behavior disorder, hallucinations, and cognitive impairment in Parkinson's disease</title></titleInfo><name type="personal"><namePart type="given">Elena</namePart><namePart type="family">Sinforiani</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Laboratory of Neuropsychology, IRCCS C. Mondino Institute of Neurology, Pavia, Italy</affiliation><description>Correspondence: IRCCS C. Mondino, Via Ferrata 6, 27100 Pavia, Italy</description><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Roberta</namePart><namePart type="family">Zangaglia</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Raffaele</namePart><namePart type="family">Manni</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Sleep Medicine Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Silvano</namePart><namePart type="family">Cristina</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Enrico</namePart><namePart type="family">Marchioni</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Laboratory of Epidemiology and Statistics, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Giuseppe</namePart><namePart type="family">Nappi</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Department of Neurology and Otolaryngology, University La Sapienza, Rome, Italy</affiliation><affiliation>IRCCS C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Francesca</namePart><namePart type="family">Mancini</namePart><namePart type="termsOfAddress">MD, PhD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Claudio</namePart><namePart type="family">Pacchetti</namePart><namePart type="termsOfAddress">MD</namePart><affiliation>Parkinson's Disease and Movement Disorders Unit, Istituto di Ricovero e Cura a Carattere Scientifico C. Mondino Institute of Neurology, Pavia, Italy</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre authority="originalCategForm">article</genre><originInfo><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><place><placeTerm type="text">Hoboken</placeTerm></place><dateIssued encoding="w3cdtf">2006-04</dateIssued><dateCaptured encoding="w3cdtf">2004-09-24</dateCaptured><dateValid encoding="w3cdtf">2005-07-03</dateValid><copyrightDate encoding="w3cdtf">2006</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType><extent unit="tables">2</extent><extent unit="references">36</extent><extent unit="words">3131</extent></physicalDescription><abstract lang="en">The objective of this study was to evaluate the relationship between REM sleep behavior disorder (RBD), hallucinations, and cognitive impairment in Parkinson's disease (PD). One hundred and ten PD patients, divided into three groups (without RBD or hallucinations; with RBD but no hallucinations; with RBD and hallucinations), were submitted to neuropsychological evaluation. The group without RBD and hallucinations showed normal neuropsychological tests when compared to normal controls. The group with hallucinations was characterized by a more severe cognitive impairment affecting both short‐ and long‐term memory, logical abilities, and frontal functions, while the RBD‐only group presented frontal impairment. The hypothesis that RBD in PD can be considered a risk factor not only of the hallucinations but also of more severe and diffuse cognitive abnormalities needs to be strengthened through a longitudinal evaluation. © 2005 Movement Disorder Society</abstract><subject lang="en"><genre>Keywords</genre><topic>Parkinson's disease</topic><topic>REM sleep behavior disorder</topic><topic>hallucinations</topic><topic>cognitive impairment</topic></subject><relatedItem type="host"><titleInfo><title>Movement Disorders</title><subTitle>Official Journal of the Movement Disorder Society</subTitle></titleInfo><titleInfo type="abbreviated"><title>Mov. Disord.</title></titleInfo><subject><genre>article category</genre><topic>Research Article</topic></subject><identifier type="ISSN">0885-3185</identifier><identifier type="eISSN">1531-8257</identifier><identifier type="DOI">10.1002/(ISSN)1531-8257</identifier><identifier type="PublisherID">MDS</identifier><part><date>2006</date><detail type="volume"><caption>vol.</caption><number>21</number></detail><detail type="issue"><caption>no.</caption><number>4</number></detail><extent unit="pages"><start>462</start><end>466</end><total>5</total></extent></part></relatedItem><identifier type="istex">0C1D10FDC9669F1C3E8E0E8E1FEB144BEB2FDB66</identifier><identifier type="DOI">10.1002/mds.20719</identifier><identifier type="ArticleID">MDS20719</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2005 Movement Disorder Society</accessCondition><recordInfo><recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin><recordContentSource>WILEY</recordContentSource></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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