dc.contributor.author | Garmendia Zaldua, Joana | |
dc.contributor.author | Labayru Isusquiza, Garazi | |
dc.contributor.author | Aliri Lazcano, Jone | |
dc.contributor.author | Winblad, Stefan | |
dc.contributor.author | Angeard, Nathalie | |
dc.contributor.author | López de Munain Arregui, Adolfo José | |
dc.contributor.author | Sistiaga Berrondo, Andone | |
dc.date.accessioned | 2024-05-27T17:20:47Z | |
dc.date.available | 2024-05-27T17:20:47Z | |
dc.date.issued | 2022-09 | |
dc.identifier.citation | Neuromuscular Disorders 32(9) : 749-753 (2022) | es_ES |
dc.identifier.issn | 1873-2364 | |
dc.identifier.issn | 0960-8966 | |
dc.identifier.uri | http://hdl.handle.net/10810/68203 | |
dc.description.abstract | Currently, 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.sponsorship | This 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.iso | eng | es_ES |
dc.publisher | Elsevier | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es/ | * |
dc.subject | myotonic dystrophy type 1 | es_ES |
dc.subject | DM1 | es_ES |
dc.subject | WAIS-IV | es_ES |
dc.subject | short-forms | es_ES |
dc.subject | intellectual functioning | es_ES |
dc.subject | cognition | es_ES |
dc.title | A validated WAIS-IV short-form to estimate intellectual functioning in myotonic dystrophy type 1 | es_ES |
dc.type | info:eu-repo/semantics/article | es_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.holder | Atribución-NoComercial-SinDerivadas 3.0 España | * |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0960896622002012 | es_ES |
dc.identifier.doi | 10.1016/j.nmd.2022.06.012 | |
dc.departamentoes | Psicología Clínica y de la Salud y Metodología de Investigación | es_ES |
dc.departamentoes | Neurociencias | es_ES |
dc.departamentoeu | Psikologia Klinikoa eta Osasunaren Psikologia eta Ikerketa Metodologia | es_ES |
dc.departamentoeu | Neurozientziak | es_ES |