Literature DB >> 28501294

Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure.

Johanna H van der Lee1, Jonathan Morton2, Heather R Adams3, Lorne Clarke4, Berendine Johanne Ebbink5, Maria L Escolar6, Roberto Giugliani7, Paul Harmatz8, Melissa Hogan9, Simon Jones10, Shauna Kearney11, Joseph Muenzer12, Stewart Rust13, Margaret Semrud-Clikeman14, Frits A Wijburg15, Zi-Fan Yu16, Darren Janzen17, Elsa Shapiro18.   

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.
Copyright © 2017 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Adaptive behavior; Clinical trial; Cognitive; Mucopolysaccharidoses; Neurological; Protocol

Mesh:

Year:  2017        PMID: 28501294     DOI: 10.1016/j.ymgme.2017.05.004

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  14 in total

Review 1.  Assessment, pharmacological therapy and rehabilitation management of musculoskeletal pain in children with mucopolysaccharidoses: a scoping review.

Authors:  R Gnasso; B Corrado; I Iommazzo; F Migliore; G Magliulo; B Giardulli; C Ruosi
Journal:  Orphanet J Rare Dis       Date:  2022-07-08       Impact factor: 4.303

2.  Quantifying medical manifestations in Hurler syndrome with the infant physical symptom score: associations with long-term physical and adaptive outcomes.

Authors:  Alia Ahmed; Kyle Rudser; Kelly E King; Julie B Eisengart; Paul J Orchard; Elsa Shapiro; Chester B Whitley
Journal:  Mol Genet Metab       Date:  2022-03-10       Impact factor: 4.204

3.  Classifying and characterizing the development of adaptive behavior in a naturalistic longitudinal study of young children with autism.

Authors:  Cristan Farmer; Lauren Swineford; Susan E Swedo; Audrey Thurm
Journal:  J Neurodev Disord       Date:  2018-01-05       Impact factor: 4.025

4.  Neurocognitive and somatic stabilization in pediatric patients with severe Mucopolysaccharidosis Type I after 52 weeks of intravenous brain-penetrating insulin receptor antibody-iduronidase fusion protein (valanafusp alpha): an open label phase 1-2 trial.

Authors:  Roberto Giugliani; Luciana Giugliani; Fabiano de Oliveira Poswar; Karina Carvalho Donis; Amauri Dalla Corte; Mathias Schmidt; Ruben J Boado; Igor Nestrasil; Carol Nguyen; Steven Chen; William M Pardridge
Journal:  Orphanet J Rare Dis       Date:  2018-07-05       Impact factor: 4.123

5.  A longitudinal study of neurocognition and behavior in patients with Hurler-Scheie syndrome heterozygous for the L238Q mutation.

Authors:  Alia Ahmed; Li Ou; Kyle Rudser; Elsa Shapiro; Julie B Eisengart; Kelly King; Agnes Chen; Patricia Dickson; Chester B Whitley
Journal:  Mol Genet Metab Rep       Date:  2019-06-27

Review 6.  Novel Enzyme Replacement Therapies for Neuropathic Mucopolysaccharidoses.

Authors:  Yuji Sato; Torayuki Okuyama
Journal:  Int J Mol Sci       Date:  2020-01-08       Impact factor: 5.923

7.  Intrafamilial variability in the clinical manifestations of mucopolysaccharidosis type II: Data from the Hunter Outcome Survey (HOS).

Authors:  Can Ficicioglu; Roberto Giugliani; Paul Harmatz; Nancy J Mendelsohn; Virginie Jego; Rossella Parini
Journal:  Am J Med Genet A       Date:  2017-12-06       Impact factor: 2.802

8.  Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome.

Authors:  Elsa G Shapiro; Chester B Whitley; Julie B Eisengart
Journal:  Orphanet J Rare Dis       Date:  2018-05-11       Impact factor: 4.123

Review 9.  Mucopolysaccharidosis Type I: A Review of the Natural History and Molecular Pathology.

Authors:  Christiane S Hampe; Julie B Eisengart; Troy C Lund; Paul J Orchard; Monika Swietlicka; Jacob Wesley; R Scott McIvor
Journal:  Cells       Date:  2020-08-05       Impact factor: 6.600

Review 10.  Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses.

Authors:  Rita Barone; Alessandra Pellico; Annarita Pittalà; Serena Gasperini
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

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