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NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2.
Monte, Thais L; Reckziegel, Estela R; Augustin, Marina C; Silva, Amanda S P; Locks-Coelho, Lucas D; Barsottini, Orlando; Pedroso, José L; Vargas, Fernando R; Saraiva-Pereira, Maria-Luiza; Leotti, Vanessa Bielefeldt; Jardim, Laura Bannach.
Afiliação
  • Monte TL; Serviço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
  • Reckziegel ER; Programa de Pós-Graduação em Ciências Médicas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Augustin MC; Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Silva ASP; Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Locks-Coelho LD; Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Barsottini O; Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
  • Pedroso JL; Setor de Neurologia Geral e Ataxias, Disciplina de Neurologia Clínica da UNIFESP-Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Vargas FR; Setor de Neurologia Geral e Ataxias, Disciplina de Neurologia Clínica da UNIFESP-Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Saraiva-Pereira ML; Laboratório de Epidemiologia de Malformações Congênitas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
  • Leotti VB; Departamento de Genética e Biologia Molecular, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Jardim LB; Serviço de Genética Médica, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Cerebellum ; 16(4): 852-858, 2017 08.
Article em En | MEDLINE | ID: mdl-28456900
ABSTRACT
Spinocerebellar ataxia type 2 (SCA2), caused by a CAG expansion (CAGexp) at ATXN2, has a complex clinical picture. While validated ataxia scales are available, comprehensive instruments to measure all SCA2 neurological manifestations are required. This study aims to validate the Neurological Examination Score for the assessment of Spinocerebellar Ataxias (NESSCA) to be used in SCA2 and to compare its responsiveness to those obtained with other instruments. NESSCA, SARA, SCAFI, and CCFS scales were applied in symptomatic SCA2 patients. Correlations were done with age at onset, disease duration, CAGexp, and between scales. Responsiveness was estimated by comparing deltas of stable to worse patients after 12 months, according to Patient Global Impression of change, and the area under the curve (AUC) of the Receiver Operating Characteristics curve of scores range. Eighty-eight evaluations (49 patients) were obtained. NESSCA had an even distribution and correlated with disease duration (r = 0.55), SARA (r = 0.63), and CAGexp (rho = 0.32) both explained 44% of NESSCA variance. Deltas (95% CI) after 1 year in stable and worse patients were only significantly different for SARA. NESSCA, SARA, SCAFI, and CCFS AUC were 0.63, 0.81, 0.49, and 0.48, respectively. NESSCA is valid to be used in SCA2. However, the only instrument that presented good responsiveness to change in 1 year was SARA. We suggest that NESSCA can be used as a secondary outcome in future trials in SCA2 due to the burden of neurological disabilities related to disease progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Ataxias Espinocerebelares / Exame Neurológico Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Gravidade de Doença / Ataxias Espinocerebelares / Exame Neurológico Tipo de estudo: Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article