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dc.rights.licenseopenen_US
hal.structure.identifierNeurocentre Magendie : Physiopathologie de la Plasticité Neuronale [U1215 Inserm - UB]
dc.contributor.authorBROCHET, Bruno
dc.contributor.authorCLAVELOU, Pierre
dc.contributor.authorDEFER, Gilles
dc.contributor.authorDE SEZE, Jerome
dc.contributor.authorLOUAPRE, Celine
dc.contributor.authorMAGNIN, Eloi
hal.structure.identifierNeurocentre Magendie : Physiopathologie de la Plasticité Neuronale [U1215 Inserm - UB]
dc.contributor.authorRUET, Aurelie
dc.contributor.authorTHOMAS-ANTERION, Catherine
dc.contributor.authorVERMERSCH, Patrick
dc.date.accessioned2022-11-08T10:58:46Z
dc.date.available2022-11-08T10:58:46Z
dc.date.issued2022-01-29
dc.identifier.issn2076-3425en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170224
dc.description.abstractEnBackground: Cognitive deficits are common in multiple sclerosis (MS) and affect patients at all stages of the disease, regardless of phenotype. Aims: This literature review focuses the cognitive deficits observed in secondary progressive MS (SPMS). It is mainly based on studies that compared the frequency and main characteristics of cognitive deficits in SPMS with other phenotypes. Methods: A bibliographic search was carried out using the PubMed database with the following keywords: multiple sclerosis, secondary-progressive, cognition. Results: Thirteen studies were initially selected that were published in English, reporting the neuropsychological data of a sample of at least 30 patients with SPMS, comparing them with patients with other phenotypes. Studies suggest that there is an association between the duration of the disease and the frequency and extent of the cognitive disorders. Studies also showed that the SP form is associated with an increased frequency of cognitive impairment and with an increased severity as compared to relapsing-remitting MS (RRMS). Compared to RRMS, progressive forms of MS are associated with more severe impairment in certain cognitive areas, such as episodic verbal memory, information processing speed, working memory, or verbal fluency. Two studies showed that cognitive performances decline overtime in SPMS. Conclusion: Cognitive disorders are more frequent and more severe in the SP form than in relapsing course of MS. The profile of cognitive impairment encountered in the SP form also appears to be different from those found in the other phenotypes. © 2022 by the authors. Licensee MDPI, Basel, Switzerland.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAttention
dc.subject.enCognition
dc.subject.enCognitive Defect
dc.subject.enDementia
dc.subject.enDemyelinating Disease
dc.subject.enDisease Duration
dc.subject.enEpisodic Memory
dc.subject.enExecutive Function
dc.subject.enExpanded Disability Status Scale
dc.subject.enGlioma
dc.subject.enHuman
dc.subject.enIcd-10
dc.subject.enMedline
dc.subject.enMental Performance
dc.subject.enMini Mental State Examination
dc.subject.enMontreal Cognitive Assessment
dc.subject.enMultiple Sclerosis
dc.subject.enNeuropsychological Test
dc.subject.enNeuropsychology
dc.subject.enNuclear Magnetic Resonance Imaging
dc.subject.enPaced Auditory Serial Addition Test
dc.subject.enParkinson Disease
dc.subject.enPhenotype
dc.subject.enPrincipal Component Analysis
dc.subject.enReview
dc.subject.enRey Auditory Verbal Learning Test
dc.subject.enSystematic Review
dc.subject.enTrail Making Test
dc.subject.enTranscranial Direct Current Stimulation
dc.subject.enVerbal Memory
dc.subject.enVisual Memory
dc.subject.enWorking Memory
dc.title.enCognitive Impairment in Secondary Progressive Multiple Sclerosis: Effect of Disease Duration, Age, and Progressive Phenotype
dc.title.alternativeBrain Sci.en_US
dc.typeArticle de revueen_US
dc.identifier.doi10.3390/brainsci12020183en_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]en_US
dc.identifier.pubmed35203948en_US
bordeaux.journalBrain Sciencesen_US
bordeaux.page183en_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesNeurocentre Magendie - U1215en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamRelations glie-neuroneen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDNovartisen_US
hal.exportfalse
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Brain%20Sciences&rft.date=2022-01-29&rft.volume=12&rft.issue=2&rft.spage=183&rft.epage=183&rft.eissn=2076-3425&rft.issn=2076-3425&rft.au=BROCHET,%20Bruno&CLAVELOU,%20Pierre&DEFER,%20Gilles&DE%20SEZE,%20Jerome&LOUAPRE,%20Celine&rft.genre=article


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