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dc.contributorInstitut d'Assistència Sanitària
dc.contributor.authorGrothe, Michel
dc.contributor.authorLabrador Espinosa, Miguel Ángel
dc.contributor.authorJesús Maestre, Silvia
dc.contributor.authorMacias-Garcia, Daniel
dc.contributor.authorAdarmes Gómez, Astrid Daniela
dc.contributor.authorCarrillo, Fátima
dc.contributor.authorSolano Vila, Berta
dc.date.accessioned2021-11-12T08:42:45Z
dc.date.available2021-11-12T08:42:45Z
dc.date.issued2021-07
dc.identifier.citationGrothe MJ, Labrador-Espinosa MA, Jesús S, Macías-García D, Adarmes-Gómez A, Carrillo F, et al. In vivo cholinergic basal forebrain degeneration and cognition in Parkinson’s disease: imaging results from the COPPADIS study. Parkinsonism Relat Disord. 2021 Jul;88:68-75.
dc.identifier.issn1873-5126
dc.identifier.urihttps://hdl.handle.net/11351/6535
dc.descriptionDiffusion tensor imaging (DTI); Nucleus basalis Meynert; Parkinson's disease
dc.description.abstractThe study included a total of 180 non-demented PD patients and 45 healthy controls, who underwent structural MRI acquisitions and standardized neurocognitive assessment through the PD-Cognitive Rating Scale (PD-CRS) within the multicentric COPPADIS-2015 study. A subset of 73 patients also had Diffusion Tensor Imaging (DTI) acquisitions. Volumetric and microstructural (mean diffusivity, MD) indices of CBF degeneration were automatically extracted using a stereotactic CBF atlas. For comparison, we also assessed multimodal indices of hippocampal degeneration. Associations between imaging measures and cognitive performance were assessed using linear models. Compared to controls, CBF volume was not significantly reduced in PD patients as a group. However, across PD patients lower CBF volume was significantly associated with lower global cognition (PD-CRStotal: r = 0.37, p < 0.001), and this association remained significant after controlling for several potential confounding variables (p = 0.004). Analysis of individual item scores showed that this association spanned executive and memory domains. No analogue cognition associations were observed for CBF MD. In covariate-controlled models, hippocampal volume was not associated with cognition in PD, but there was a significant association for hippocampal MD (p = 0.02). Early cognitive deficits in PD without dementia are more closely related to structural MRI measures of CBF degeneration than hippocampal degeneration. In our multicentric imaging acquisitions, DTI-based diffusion measures in the CBF were inferior to standard volumetric assessments for capturing cognition-relevant changes in non-demented PD.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofseriesParkinsonism and Related Disorders;88
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectParkinson, Malaltia de
dc.subjectRessonància magnètica
dc.subjectCervell - Imatgeria per ressonància magnètica
dc.subject.meshParkinson Disease
dc.subject.meshDiffusion Tensor Imaging
dc.subject.meshBasal Nucleus of Meynert
dc.titleIn vivo cholinergic basal forebrain degeneration and cognition in Parkinson’s disease: imaging results from the COPPADIS study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.parkreldis.2021.05.027.
dc.subject.decsenfermedad de Parkinson
dc.subject.decsimagen por resonancia magnética
dc.subject.decsnúcleo basal de Meynert
dc.relation.publishversionhttps://doi.org/10.1016/j.parkreldis.2021.05.027
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.event.productorBiblioteca
dc.contributor.authoraffiliation[Grothe MJ, Labrador-Espinosa MA, Jesús S, Macías-García D, Adarmes-Gómez A] Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain. Centro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED), Instituto de Salud Carlos III, Madrid, Spain. [Carrillo F] Unidad de Trastornos del Movimiento, Servicio de Neurología y Neurofisiología Clínica, Instituto de Biomedicina de Sevilla (IBiS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Seville, Spain. [Solano Vila B] Institut Catalá de la Salut (ICS), Girona, Spain. Institut d'Assisténcia Sanitaria (IAS), Salt, Spain
dc.identifier.pmid34144230
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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