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dc.contributorHospital General de Granollers
dc.contributor.authorRoura Blanco, Ignacio
dc.contributor.authorPardo Ruiz, Jèssica
dc.contributor.authorMartin Barcelo, Cristina
dc.contributor.authorOltra González, Javier
dc.contributor.authorCampabadal Delgado, Anna
dc.contributor.authorSala-Llonch, Roser
dc.contributor.authorPont-Sunyer, Claustre
dc.date.accessioned2025-02-21T07:48:56Z
dc.date.available2025-02-21T07:48:56Z
dc.date.issued2025-01-28
dc.identifier.citationRoura I, Pardo J, Martín-Barceló C, Oltra J, Campabadal A, Sala-Llonch R, et al. Altered Intra- and Inter-Network Resting-State Functional Connectivity is Associated with Neuropsychological Functioning and Clinical Symptoms in Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder. Mov Disord. 2025 Jan 28.
dc.identifier.issn0885-3185
dc.identifier.urihttps://hdl.handle.net/11351/12632
dc.descriptionIsolated rapid-eye movement (REM); Magnetic resonance imaging (rsfMRI); Comprehensive neuropsychological testing
dc.description.abstractBackground: Isolated rapid-eye movement (REM) sleep behavior disorder (iRBD) is characterized by abnormal behaviors in REM sleep and is considered as a prodromal symptom of alpha-synucleinopathies. Resting-state functional magnetic resonance imaging (rsfMRI) studies have unveiled altered functional connectivity (rsFC) in patients with iRBD. However, the associations between intra- and inter-network rsFC with clinical symptoms and neuropsychological functioning in iRBD remain unclear. Objective: To characterize intra- and inter-network rsFC in iRBD patients using a data-driven approach and to assess its associations with clinical features and cognitive functioning. Methods: Forty-two patients with iRBD and 45 healthy controls (HC) underwent rsfMRI and comprehensive neuropsychological testing. Resting-state networks were characterized using independent component analyses. Group differences in intra- and inter-network rsFC and their associations with clinical and neuropsychological data were studied. A threshold of corrected P < 0.05 was used in all the analyses. Results: iRBD patients displayed lower intra-network rsFC within basal ganglia, visual, sensorimotor, and cerebellar networks, relative to HC. Mean rsFC strength within the basal ganglia network positively correlated with processing speed and negatively with the non-motor symptoms in iRBD patients. Reduced inter-network rsFC between sensorimotor and visual medial networks was observed in iRBD patients, which was associated with global cognitive status. Conclusions: iRBD is characterized by both reductions in intra-network rsFC in cortical and subcortical networks and inter-network dysconnectivity between sensorimotor and visual networks. Abnormalities in intra- and inter-network rsFC are associated with cognitive performance and non-motor symptoms, suggesting the utility of both rsFC measures as imaging markers in prodromal alpha-synucleinopathies. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesMovement disorders;
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectUlls - Moviments
dc.subjectRessonància magnètica
dc.subjectTrastorns del son
dc.subject.meshNeuropsychology
dc.subject.meshREM Sleep Behavior Disorder
dc.subject.meshFunctional Neuroimaging
dc.titleAltered Intra- and Inter-Network Resting-State Functional Connectivity is Associated with Neuropsychological Functioning and Clinical Symptoms in Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1002/mds.30126
dc.subject.decsneuropsicología
dc.subject.decstrastorno de la conducta en el sueño REM
dc.subject.decsneuroimágenes funcionales
dc.relation.publishversionhttps://doi.org/10.1002/mds.30126
dc.type.versioninfo:eu-repo/semantics/acceptedVersion
dc.audienceProfessionals
dc.contributor.authoraffiliation[Roura I, Pardo J, Martín-Barceló C] Medical Psychology Unit, Department of Medicine, Institute of Neurosciences, University of Barcelona, Barcelona, Spain. Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. [Oltra J] Medical Psychology Unit, Department of Medicine, Institute of Neurosciences, University of Barcelona, Barcelona, Spain. Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Aging Research Center, Department of Neurobiology, Care Sciences, and Society, Karolinska Institutet, Stockholm, Sweden. [Campabadal A] Medical Psychology Unit, Department of Medicine, Institute of Neurosciences, University of Barcelona, Barcelona, Spain. Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Neurology Service, Consorci Corporació Sanitària Parc Taulí de Sabadell, Barcelona, Spain. [Sala-Llonch R] Institut d’Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. Department of Biomedicine, Institut de Neurociències University of Barcelona, Barcelona, Spain. Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Barcelona, Spain. [Pont-Sunyer C] Servei de Neurologia Unitat de Trastorns del Moviment, Hospital General de Granollers, Granollers, Spain
dc.identifier.pmid39876613
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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