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dc.rights.licenseopenen_US
hal.structure.identifierLaboratoire de psychologie:Santé et qualité de vie
dc.contributor.authorCHEVALERE, Johann
dc.contributor.authorJAUREGI, J.
dc.contributor.authorCOPET, P.
dc.contributor.authorLAURIER, Virginie
dc.contributor.authorTHUILLEAUX, Denise
hal.structure.identifierLaboratoire de psychologie:Santé et qualité de vie
dc.contributor.authorPOSTAL, Virginie
dc.date.accessioned2021-06-01T09:42:50Z
dc.date.available2021-06-01T09:42:50Z
dc.date.issued2019-02-01
dc.identifier.issn0891-4222en_US
dc.identifier.urioai:crossref.org:10.1016/j.ridd.2018.11.013
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/78783
dc.description.abstractEnBackground: Recent work suggests that maladaptive behaviors in genetic developmental disorders may emerge from autonomic dysfunctions impacting higher order executive functions. In Prader-Willi syndrome (PWS), executive functions are not well understood and investigations of possible underlying causes at the autonomic level are lacking. Aims: This study aimed at clarifying the status of inhibition and working memory updating functions in PWS and searched for sympathetic signatures as well as to examine their links with executive performance. Methods and Procedures: The performance of thirty adults with PWS was compared to that of thirty healthy adults on two tasks assessing inhibition and working memory updating while electrodermal activity (EDA) was recorded. Outcomes and Results: PWS adults underperformed healthy adults in the inhibition and the working memory updating tasks and showed abnormal skin conductance responses. Distinct EDA have been found in PWS and healthy adults. Furthermore, while EDA reflected distinct cognitive processes, correlations between electrodermal and behavioural data were absent when examining the two groups separately. Conclusions and Implications: PWS is associated with a slight impairment of inhibition and a severe impairment of working memory updating. Furthermore, there are specific sympathetic autonomic signatures in PWS that do not present straightforward links with executive dysfunctions.
dc.language.isoENen_US
dc.sourcecrossref
dc.subject.enPrader-Willi syndrome
dc.subject.enExecutive functions
dc.subject.enElectrodermal activity
dc.title.enInvestigation of the relationship between electrodermal and behavioural responses to executive tasks in Prader-Willi syndrome: An event-related experiment
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.ridd.2018.11.013en_US
dc.subject.halSciences de l'Homme et Société/Psychologieen_US
dc.identifier.pubmed30590308en_US
bordeaux.journalResearch in Developmental Disabilitiesen_US
bordeaux.page229-242en_US
bordeaux.volume85en_US
bordeaux.hal.laboratoriesLaboratoire de psychologie (LabPsy) - EA4139en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
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hal.identifierhal-03244506
hal.version1
hal.date.transferred2021-06-01T09:42:53Z
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