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Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure.
van der Lee, Johanna H; Morton, Jonathan; Adams, Heather R; Clarke, Lorne; Ebbink, Berendine Johanne; Escolar, Maria L; Giugliani, Roberto; Harmatz, Paul; Hogan, Melissa; Jones, Simon; Kearney, Shauna; Muenzer, Joseph; Rust, Stewart; Semrud-Clikeman, Margaret; Wijburg, Frits A; Yu, Zi-Fan; Janzen, Darren; Shapiro, Elsa.
Afiliación
  • van der Lee JH; Pediatric Clinical Research Office, Emma Children's Hospital, Academic Medical Center, Amsterdam, Netherlands.
  • Morton J; Comradis Limited, Oxford, UK.
  • Adams HR; Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
  • Clarke L; British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
  • Ebbink BJ; Center for Lysosomal and Metabolic Diseases, Erasmus MC University Medical Center, Rotterdam, Netherlands.
  • Escolar ML; Department of Pediatrics, Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Giugliani R; Department of Genetics/UFRGS, Medical Genetic Service/HCPA, Porto Alegre, Brazil.
  • Harmatz P; UCSF Benioff Children's Hospital Oakland, Oakland, CA, USA.
  • Hogan M; Saving Case & Friends, Thompsons Station, TN, USA.
  • Jones S; Willink Biochemical Genetic Unit, Manchester Centre for Genomic Medicine, Saint Mary's Hospital, Manchester, UK.
  • Kearney S; Clinical Paediatric Psychology, Birmingham Children's Hospital NHS Foundation Trust, Birmingham, UK.
  • Muenzer J; Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
  • Rust S; Paediatric Psychosocial Department, Royal Manchester Children's Hospital, Manchester, UK.
  • Semrud-Clikeman M; Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.
  • Wijburg FA; Department of Pediatrics, Academic Medical Center, Amsterdam, Netherlands.
  • Yu ZF; Statistics Collaborative, Inc., Washington, DC, USA.
  • Janzen D; Institute on Development & Disability, Oregon Health & Science University, Portland, OR, USA.
  • Shapiro E; Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA; Shapiro Neuropsychology Consulting, LLC, Portland, OR, USA. Electronic address: shapi004@umn.edu.
Mol Genet Metab ; 121(2): 70-79, 2017 06.
Article en En | MEDLINE | ID: mdl-28501294
ABSTRACT
The design and conduct of clinical studies to evaluate the effects of novel therapies on central nervous system manifestations in children with neuronopathic mucopolysaccharidoses is challenging. Owing to the rarity of these disorders, multinational studies are often needed to recruit enough patients to provide meaningful data and statistical power. This can make the consistent collection of reliable data across study sites difficult. To address these challenges, an International MPS Consensus Conference for Cognitive Endpoints was convened to discuss approaches for evaluating cognitive and adaptive function in patients with mucopolysaccharidoses. The goal was to develop a consensus on best practice for the design and conduct of clinical studies investigating novel therapies for these conditions, with particular focus on the most appropriate outcome measures for cognitive function and adaptive behavior. The outcomes from the consensus panel discussion are reported here.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis / Cognición Tipo de estudio: Guideline Límite: Child / Humans Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mucopolisacaridosis / Cognición Tipo de estudio: Guideline Límite: Child / Humans Idioma: En Año: 2017 Tipo del documento: Article