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dc.contributor.authorGarmendia Zaldua, Joana
dc.contributor.authorLabayru Isusquiza, Garazi
dc.contributor.authorAliri Lazcano, Jone ORCID
dc.contributor.authorWinblad, Stefan
dc.contributor.authorAngeard, Nathalie
dc.contributor.authorLópez de Munain Arregui, Adolfo José
dc.contributor.authorSistiaga Berrondo, Andone ORCID
dc.date.accessioned2024-05-27T17:20:47Z
dc.date.available2024-05-27T17:20:47Z
dc.date.issued2022-09
dc.identifier.citationNeuromuscular Disorders 32(9) : 749-753 (2022)es_ES
dc.identifier.issn1873-2364
dc.identifier.issn0960-8966
dc.identifier.urihttp://hdl.handle.net/10810/68203
dc.description.abstractCurrently, no rapid and specific instrument is available to briefly estimate intelligence in patients with myotonic dystrophy type 1 (DM1), a multisystemic disease that involves the CNS and is associated with cognitive deficits and low intellectual functioning. This study aimed to develop a DM1-specific and valid short-form of the Wechsler Adult Intelligence Scale-Fourth Edition (WAIS-IV) to estimate intellectual functioning in this population. Thirty non-congenital DM1 patients (10 female; mean age=46.77; SD= 9.76) were assessed with the WAIS-IV. Data were analyzed following two independent strategies: A) multiple linear regression with the aim of maintaining the scale's factorial structure; and B) correlational analyses between scores on all WAIS-IV subtests and Full-Scale IQ (FSIQ). Validity of the resulting short-forms was also analyzed. Three short-forms were developed: Proposal A from strategy A (Vocabulary, Block Design, Arithmetic and Symbol Search), Proposal B1 (Vocabulary, Block Design, Digit Span and Visual Puzzles) and Proposal B2 (Vocabulary and Block Design), from strategy B. All three short-forms showed a strong and significant correlation with the FSIQ and were considered psychometrically acceptable. Arguments in favor of Proposal B1 are discussed. Assessing FSIQ with these short-forms will be useful for avoiding long assessment procedures in a population characterized by high fatigability.es_ES
dc.description.sponsorshipThis work was supported by Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (Ref: 609), from the Institute of Health Carlos III co-founded by Fondo Europeo de Desarrollo Regional [PI17/01231 to A.S.; PI17/01841 to A.L.]; Basque Government [S-PE13UN030 to A.S.]; and University of the Basque Country [PIF 20/238 to J.G.; GU 20/057 to J.G., G.L., and A.S.].es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectmyotonic dystrophy type 1es_ES
dc.subjectDM1es_ES
dc.subjectWAIS-IVes_ES
dc.subjectshort-formses_ES
dc.subjectintellectual functioninges_ES
dc.subjectcognitiones_ES
dc.titleA validated WAIS-IV short-form to estimate intellectual functioning in myotonic dystrophy type 1es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0960896622002012es_ES
dc.identifier.doi10.1016/j.nmd.2022.06.012
dc.departamentoesPsicología Clínica y de la Salud y Metodología de Investigaciónes_ES
dc.departamentoesNeurocienciases_ES
dc.departamentoeuPsikologia Klinikoa eta Osasunaren Psikologia eta Ikerketa Metodologiaes_ES
dc.departamentoeuNeurozientziakes_ES


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© 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
(http://creativecommons.org/licenses/by-nc-nd/4.0/)
Except where otherwise noted, this item's license is described as © 2022 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)