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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorSantos-García, Diego
dc.contributor.authorde Deus, Teresa
dc.contributor.authorCores, Carlos
dc.contributor.authorCanfield, Hector
dc.contributor.authorPaz González, Jose M
dc.contributor.authorMartínez Miró, Cristina
dc.contributor.authorHernández Vara, Jorge
dc.contributor.authorde Fabregues-Boixar Nebot, Oriol
dc.date.accessioned2022-03-17T09:36:12Z
dc.date.available2022-03-17T09:36:12Z
dc.date.issued2021-06-30
dc.identifier.citationSantos-García D, de Deus T, Cores C, Canfield H, Paz González J, Martínez Miró C, et al. Predictors of Global Non-Motor Symptoms Burden Progression in Parkinson’s Disease. Results from the COPPADIS Cohort at 2-Year Follow-Up. J Pers Med. 2021 Jun 30;11(7):626.
dc.identifier.issn2075-4426
dc.identifier.urihttps://hdl.handle.net/11351/7197
dc.descriptionParkinson’s disease; Non-motor symptoms; Progression
dc.description.abstractBackground and Objective: Non-motor symptoms (NMS) progress in different ways between Parkinson’s disease (PD) patients. The aim of the present study was to (1) analyze the change in global NMS burden in a PD cohort after a 2-year follow-up, (2) to compare the changes with a control group, and (3) to identify predictors of global NMS burden progression in the PD group. Material and Methods: PD patients and controls, recruited from 35 centers of Spain from the COPPADIS cohort from January 2016 to November 2017, were followed-up with after 2 years. The Non-Motor Symptoms Scale (NMSS) was administered at baseline (V0) and at 24 months ± 1 month (V2). Linear regression models were used for determining predictive factors of global NMS burden progression (NMSS total score change from V0 to V2 as dependent variable). Results: After the 2-year follow-up, the mean NMS burden (NMSS total score) significantly increased in PD patients by 18.8% (from 45.08 ± 37.62 to 53.55 ± 42.28; p < 0.0001; N = 501; 60.2% males, mean age 62.59 ± 8.91) compared to no change observed in controls (from 14.74 ± 18.72 to 14.65 ± 21.82; p = 0.428; N = 122; 49.5% males, mean age 60.99 ± 8.32) (p < 0.0001). NMSS total score at baseline (β = −0.52), change from V0 to V2 in PDSS (Parkinson’s Disease Sleep Scale) (β = −0.34), and change from V0 to V2 in NPI (Neuropsychiatric Inventory) (β = 0.25) provided the highest contributions to the model (adjusted R-squared 0.41; Durbin-Watson test = 1.865). Conclusions: Global NMS burden demonstrates short-term progression in PD patients but not in controls and identifies worsening sleep problems and neuropsychiatric symptoms as significant independent predictors of this NMS progression.
dc.language.isoeng
dc.publisherMDPI
dc.relation.ispartofseriesJournal of Personalized Medicine;11(7)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectQualitat de vida
dc.subjectSímptomes
dc.subjectParkinson, Malaltia de - Diagnòstic
dc.subject.meshParkinson Disease
dc.subject.mesh/diagnosis
dc.subject.meshQuality of Life
dc.subject.meshSigns and Symptoms
dc.titlePredictors of Global Non-Motor Symptoms Burden Progression in Parkinson's Disease. Results from the COPPADIS Cohort at 2-Year Follow-Up
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/jpm11070626
dc.subject.decsenfermedad de Parkinson
dc.subject.decs/diagnóstico
dc.subject.decscalidad de vida
dc.subject.decssignos y síntomas
dc.relation.publishversionhttps://doi.org/10.3390/jpm11070626
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Santos García D, Cores C, Paz González JM, Martínez Miró C] CHUAC, Complejo Hospitalario Universitario de A Coruña, A Coruña, Spain. [de Deus T, Canfield H] CHUF, Complejo Hospitalario Universitario de Ferrol, A Coruña, Spain. [Hernández-Vara J, de Fábregues O] Vall d’Hebron Hospital Universitari, Barcelona, Spain
dc.identifier.pmid34209166
dc.identifier.wos000676656900001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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