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Dysarthria in hereditary spastic paraplegia type 4
Jacinto-Scudeiro, Lais Alves; Rothe-Neves, Rui; Santos, Vanessa Brzoskowski dos; Machado, Gustavo Dariva; Burguêz, Daniela; Padovani, Marina Martins Pereira; Ayres, Annelise; Rech, Rafaela Soares; González-Salazar, Carelis; França Junior, Marcondes Cavalcante; Saute, Jonas Alex Morales; Olchik, Maira Rozenfeld.
Afiliação
  • Jacinto-Scudeiro, Lais Alves; Universidade Federal do Rio Grande do Sul. Medical Sciences. Postgraduate Program in Medicine. Porto Alegre. BR
  • Rothe-Neves, Rui; Universidade Federal de Minas Gerais. Phonetics Laboratory of the Faculty of Letters. Belo Horizonte. BR
  • Santos, Vanessa Brzoskowski dos; Universidade Federal do Rio Grande do Sul. Medical Sciences. Postgraduate Program in Medicine. Porto Alegre. BR
  • Machado, Gustavo Dariva; Hospital de Clínicas de Porto Alegre. Medical Genetics Service. Porto Alegre. BR
  • Burguêz, Daniela; Hospital de Clínicas de Porto Alegre. Medical Genetics Service. Porto Alegre. BR
  • Padovani, Marina Martins Pereira; Faculdade de Ciências Médicas da Santa Casa de São Paulo. São Paulo. BR
  • Ayres, Annelise; Universidade Federal de Ciências da Saúde de Porto Alegre. Porto Alegre. BR
  • Rech, Rafaela Soares; Universidade Federal de Ciências da Saúde de Porto Alegre. Porto Alegre. BR
  • González-Salazar, Carelis; Universidade Estadual de Campinas. Postgraduate Program in Medical Pathophysiology. São Paulo. BR
  • França Junior, Marcondes Cavalcante; Universidade Estadual de Campinas. Department of Neurology. São Paulo. BR
  • Saute, Jonas Alex Morales; Universidade Federal do Rio Grande do Sul. Medical Sciences. Postgraduate Program in Medicine. Porto Alegre. BR
  • Olchik, Maira Rozenfeld; Universidade Federal do Rio Grande do Sul. Medical Sciences. Postgraduate Program in Medicine. Porto Alegre. BR
Clinics ; 78: 100128, 2023. tab
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1421267
Biblioteca responsável: BR1.1
ABSTRACT
Abstract Objective: To describe the speech pattern of patients with hereditary Spastic Paraplegia type 4 (SPG4) and correlated it with their clinical data. Methods: Cross-sectional study was carried out in two university hospitals in Brazil. Two groups participated in the study: the case group (n = 28) with a confirmed genetic diagnosis for SPG4 and a control group (n = 17) matched for sex and age. The speech assessment of both groups included: speech task recording, acoustic analysis, and auditory-perceptual analysis. In addition, disease severity was assessed with the Spastic Paraplegia Rating Scale (SPRS). Results: In the auditory-perceptual analysis, 53.5% (n = 15) of individuals with SPG4 were dysarthric, with mild to moderate changes in the subsystems of phonation and articulation. On acoustic analysis, SPG4 subjects' performances were worse in measurements related to breathing (maximum phonation time) and articulation (speech rate, articulation rate). The articulation variables (speech rate, articulation rate) are related to the age of onset of the first motor symptom. Conclusion: Dysarthria in SPG4 is frequent and mild, and it did not evolve in conjunction with more advanced motor diseases. This data suggest that diagnosed patients should be screened and referred for speech therapy evaluation and those pathophysiological mechanisms of speech involvement may differ from the length-dependent degeneration of the corticospinal tract.


Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Tipo de estudo: Estudo observacional Idioma: Inglês Revista: Clinics Ano de publicação: 2023 Tipo de documento: Artigo / Documento de projeto

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Texto completo: Disponível Coleções: Bases de dados internacionais Base de dados: LILACS Tipo de estudo: Estudo observacional Idioma: Inglês Revista: Clinics Ano de publicação: 2023 Tipo de documento: Artigo / Documento de projeto