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Multi-disease validation of the RUDAS for cognitive screening in Alzheimer’s disease, Parkinson’s disease, and multiple sclerosis

dc.contributor.authorDelgado Álvarez, Alfonso
dc.contributor.authorDíez Cirarda, María
dc.contributor.authorDelgado Alonso, Cristina
dc.contributor.authorHernández Lorenzo, Laura
dc.contributor.authorCuevas, Constanza
dc.contributor.authorValles Salgado, María
dc.contributor.authorMontero Escribano, Paloma
dc.contributor.authorGil Moreno, María José
dc.contributor.authorMatías-Guiu Guía, Jorge
dc.contributor.authorGarcía-Ramos García, María Del Rocío
dc.contributor.authorMatias-Guiu, Jordi A.
dc.date.accessioned2024-05-14T13:00:54Z
dc.date.available2024-05-14T13:00:54Z
dc.date.issued2023-01-17
dc.description.abstractBackground: The Rowland Universal Dementia Assessment Scale (RUDAS) is a cognitive test with favorable diagnostic properties for detecting dementia and a low influence of education and cultural biases. Objective: We aimed to validate the RUDAS in people with Alzheimer’s disease (AD), Parkinson’s disease (PD), and multiple sclerosis (MS). Methods: We enrolled one hundred and fifty participants (60 with AD, 30 with PD, 60 with MS, and 120 healthy controls (HC)). All clinical groups completed a comprehensive neuropsychological battery, RUDAS, and standard cognitive tests of each disorder: MMSE, SCOPA-COG, and Symbol Digit Modalities Test. Intergroup comparisons between clinical groups and HC and ROC curves were estimated. Random Forest algorithms were trained and validated to detect cognitive impairment using RUDAS and rank the most relevant scores. Results: The RUDAS scores were lower in patients with AD, and patients with PD and MS showed cognitive impairment compared to healthy controls. Effect sizes were generally large. The total score was the most discriminative, followed by the memory score. Correlations with standardized neuropsychological tests were moderate to high. Random Forest algorithms obtained accuracies over 80–90% using the RUDAS for diagnosing AD and cognitive impairment associated with PD and MS. Conclusion: Our results suggest the RUDAS is a valid test candidate for multi-disease cognitive screening tool in AD, PD, and MS.en
dc.description.departmentDepto. de Psicobiología y Metodología en Ciencias del Comportamiento
dc.description.departmentDepto. de Medicina
dc.description.departmentDepto. de Arquitectura de Computadores y Automática
dc.description.facultyFac. de Psicología
dc.description.facultyFac. de Medicina
dc.description.facultyFac. de Informática
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipComisión Europea
dc.description.statuspub
dc.identifier.citationDelgado-Álvarez A, Díez-Cirarda M, Delgado-Alonso C, Hernández-Lorenzo L, Cuevas C, Valles-Salgado M, et al. Multi-Disease Validation of the RUDAS for Cognitive Screening in Alzheimer’s Disease, Parkinson’s Disease, and Multiple Sclerosis. JAD 2023;91:705–17. https://doi.org/10.3233/JAD-220907.
dc.identifier.doi10.3233/jad-220907
dc.identifier.issn1387-2877
dc.identifier.issn1875-8908
dc.identifier.officialurlhttps://doi.org/10.3233/jad-220907
dc.identifier.relatedurlhttps://content.iospress.com/articles/journal-of-alzheimers-disease/jad220907
dc.identifier.urihttps://hdl.handle.net/20.500.14352/104011
dc.issue.number2
dc.journal.titleJournal of Alzheimer’s Disease
dc.language.isoeng
dc.page.final717
dc.page.initial705
dc.publisherIOS Press
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020 (ISCIII)/PI19%2F01260/ES/EVALUACION NEUROPSICOLOGICA TRANSCULTURAL/
dc.relation.projectIDINT20/00079
dc.rights.accessRightsrestricted access
dc.subject.keywordAlzheimer’s disease
dc.subject.keywordCognitive screening test
dc.subject.keywordMultiple sclerosis
dc.subject.keywordParkinson’s disease
dc.subject.keywordRUDAS
dc.subject.ucmNeuropsicología
dc.subject.unesco3205.07 Neurología
dc.titleMulti-disease validation of the RUDAS for cognitive screening in Alzheimer’s disease, Parkinson’s disease, and multiple sclerosisen
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number91
dspace.entity.typePublication
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relation.isAuthorOfPublicationc86a8fee-473f-4ab8-9992-7f313064a008
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relation.isAuthorOfPublication.latestForDiscoveryd4ae3c31-bf3c-426c-8540-66134aad8381

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