Literature DB >> 26095521

Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatment.

Elsa G Shapiro1, Igor Nestrasil2, Kyle Rudser2, Kathleen Delaney2, Victor Kovac2, Alia Ahmed2, Brianna Yund2, Paul J Orchard2, Julie Eisengart2, Gregory R Niklason2, Julian Raiman3, Eva Mamak4, Morton J Cowan5, Mara Bailey-Olson5, Paul Harmatz6, Suma P Shankar7, Stephanie Cagle7, Nadia Ali7, Robert D Steiner8, Jeffrey Wozniak2, Kelvin O Lim2, Chester B Whitley2.   

Abstract

OBJECTIVES: Precise characterization of cognitive outcomes and factors that contribute to cognitive variability will enable better understanding of disease progression and treatment effects in mucopolysaccharidosis type I (MPS I). We examined the effects on cognition of phenotype, genotype, age at evaluation and first treatment, and somatic disease burden.
METHODS: Sixty patients with severe MPS IH (Hurler syndrome treated with hematopoietic cell transplant and 29 with attenuated MPS I treated with enzyme replacement therapy), were studied with IQ measures, medical history, genotypes. Sixty-seven patients had volumetric MRI. Subjects were grouped by age and phenotype and MRI and compared to 96 normal controls.
RESULTS: Prior to hematopoietic cell transplant, MPS IH patients were all cognitively average, but post-transplant, 59% were below average, but stable. Genotype and age at HCT were associated with cognitive ability. In attenuated MPS I, 40% were below average with genotype and somatic disease burden predicting their cognitive ability. White matter volumes were associated with IQ for controls, but not for MPS I. Gray matter volumes were positively associated with IQ in controls and attenuated MPS I patients, but negatively associated in MPS IH.
CONCLUSIONS: Cognitive impairment, a major difficulty for many MPS I patients, is associated with genotype, age at treatment and somatic disease burden. IQ association with white matter differed from controls. Many attenuated MPS patients have significant physical and/or cognitive problems and receive insufficient support services. Results provide direction for future clinical trials and better disease management.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Genotypes; Mucopolysaccharidosis Type I; Neurocognition; Neuroimaging

Mesh:

Year:  2015        PMID: 26095521      PMCID: PMC4561597          DOI: 10.1016/j.ymgme.2015.06.002

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


  39 in total

1.  Musculoskeletal manifestations of Hurler syndrome: long-term follow-up after bone marrow transplantation.

Authors:  Jason S Weisstein; Eliana Delgado; Lynne S Steinbach; Kim Hart; Seymour Packman
Journal:  J Pediatr Orthop       Date:  2004 Jan-Feb       Impact factor: 2.324

2.  Brain MRI findings in patients with mucopolysaccharidosis types I and II and mild clinical presentation.

Authors:  M Gisele Matheus; Mauricio Castillo; J Keith Smith; Diane Armao; Diane Towle; Joseph Muenzer
Journal:  Neuroradiology       Date:  2004-06-17       Impact factor: 2.804

Review 3.  Neurocognitive late effects of chemotherapy in children: the past 10 years of research on brain structure and function.

Authors:  Fiona S Anderson; Alicia S Kunin-Batson
Journal:  Pediatr Blood Cancer       Date:  2009-02       Impact factor: 3.167

Review 4.  The future for treatment by bone marrow transplantation for adrenoleukodystrophy, metachromatic leukodystrophy, globoid cell leukodystrophy and Hurler syndrome.

Authors:  W Krivit; L A Lockman; P A Watkins; J Hirsch; E G Shapiro
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

5.  Enzyme replacement is associated with better cognitive outcomes after transplant in Hurler syndrome.

Authors:  Julie B Eisengart; Kyle D Rudser; Jakub Tolar; Paul J Orchard; Teresa Kivisto; Richard S Ziegler; Chester B Whitley; Elsa G Shapiro
Journal:  J Pediatr       Date:  2012-09-10       Impact factor: 4.406

Review 6.  Mucopolysaccharidosis type I: current knowledge on its pathophysiological mechanisms.

Authors:  Derbis Campos; Madelyn Monaga
Journal:  Metab Brain Dis       Date:  2012-04-14       Impact factor: 3.584

7.  Features of brain MRI in dogs with treated and untreated mucopolysaccharidosis type I.

Authors:  Charles H Vite; Igor Nestrasil; Anton Mlikotic; Jackie K Jens; Elizabeth M Snella; William Gross; Elsa G Shapiro; Victor Kovac; James M Provenzale; Steven Chen; Steven Q Le; Shih-hsin Kan; Shida Banakar; Raymond Y Wang; Mark E Haskins; N Matthew Ellinwood; Patricia I Dickson
Journal:  Comp Med       Date:  2013-04       Impact factor: 0.982

8.  Mutational and oxidative stress analysis in patients with mucopolysaccharidosis type I undergoing enzyme replacement therapy.

Authors:  Vanessa Gonçalves Pereira; Ana Maria Martins; Cecília Micheletti; Vânia D'Almeida
Journal:  Clin Chim Acta       Date:  2007-09-19       Impact factor: 3.786

Review 9.  Methods for assessing neurodevelopment in lysosomal storage diseases and related disorders: a multidisciplinary perspective.

Authors:  Holly R Martin; Michele D Poe; Debra Reinhartsen; Rebecca E Pretzel; Jackson Roush; Angela Rosenberg; Stacey C Dusing; Maria L Escolar
Journal:  Acta Paediatr       Date:  2008-04       Impact factor: 2.299

10.  Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources.

Authors:  G Souillet; N Guffon; I Maire; M Pujol; P Taylor; F Sevin; N Bleyzac; C Mulier; A Durin; K Kebaili; C Galambrun; Y Bertrand; R Froissart; C Dorche; L Gebuhrer; C Garin; J Berard; P Guibaud
Journal:  Bone Marrow Transplant       Date:  2003-06       Impact factor: 5.483

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  29 in total

Review 1.  Lysosomal storage disease overview.

Authors:  Angela Sun
Journal:  Ann Transl Med       Date:  2018-12

2.  Social Functioning and Behaviour in Mucopolysaccharidosis IH [Hurlers Syndrome].

Authors:  Annukka Lehtonen; Stewart Rust; Simon Jones; Richard Brown; Dougal Hare
Journal:  JIMD Rep       Date:  2017-07-29

3.  Evaluation of non-reducing end pathologic glycosaminoglycan detection method for monitoring therapeutic response to enzyme replacement therapy in human mucopolysaccharidosis I.

Authors:  Moin U Vera; Steven Q Le; Alla Victoroff; Merry B Passage; Jillian R Brown; Brett E Crawford; Lynda E Polgreen; Agnes H Chen; Patricia I Dickson
Journal:  Mol Genet Metab       Date:  2019-09-11       Impact factor: 4.797

4.  Quantitative brain MRI morphology in severe and attenuated forms of mucopolysaccharidosis type I.

Authors:  Victor Kovac; Elsa G Shapiro; Kyle D Rudser; Bryon A Mueller; Julie B Eisengart; Kathleen A Delaney; Alia Ahmed; Kelly E King; Brianna D Yund; Morton J Cowan; Julian Raiman; Eva G Mamak; Paul R Harmatz; Suma P Shankar; Nadia Ali; Stephanie R Cagle; Jeffrey R Wozniak; Kelvin O Lim; Paul J Orchard; Chester B Whitley; Igor Nestrasil
Journal:  Mol Genet Metab       Date:  2022-01-07       Impact factor: 4.797

5.  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

6.  Intrathecal enzyme replacement for cognitive decline in mucopolysaccharidosis type I, a randomized, open-label, controlled pilot study.

Authors:  Agnes H Chen; Paul Harmatz; Igor Nestrasil; Julie B Eisengart; Kelly E King; Kyle Rudser; Alexander M Kaizer; Alena Svatkova; Amy Wakumoto; Steven Q Le; Jacqueline Madden; Sarah Young; Haoyue Zhang; Lynda E Polgreen; Patricia I Dickson
Journal:  Mol Genet Metab       Date:  2019-11-30       Impact factor: 4.797

7.  Myelin and Lipid Composition of the Corpus Callosum in Mucopolysaccharidosis Type I Mice.

Authors:  Steven Q Le; Igor Nestrasil; Shih-Hsin Kan; Martin Egeland; Jonathan D Cooper; David Elashoff; Rong Guo; Jakub Tolar; Jennifer K Yee; Patricia I Dickson
Journal:  Lipids       Date:  2020-06-14       Impact factor: 1.880

8.  Attention and corpus callosum volumes in individuals with mucopolysaccharidosis type I.

Authors:  Kelly E King; Kyle D Rudser; Igor Nestrasil; Victor Kovac; Kathleen A Delaney; Jeffrey R Wozniak; Bryon A Mueller; Kelvin O Lim; Julie B Eisengart; Eva G Mamak; Julian Raiman; Nadia Ali; Stephanie Cagle; Paul Harmatz; Chester B Whitley; Elsa G Shapiro
Journal:  Neurology       Date:  2019-04-12       Impact factor: 9.910

Review 9.  Cognitive outcomes and age of detection of severe mucopolysaccharidosis type 1.

Authors:  Scott D Grosse; Wendy K K Lam; Lisa D Wiggins; Alex R Kemper
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

Review 10.  Update on Clinical Ex Vivo Hematopoietic Stem Cell Gene Therapy for Inherited Monogenic Diseases.

Authors:  Francesca Tucci; Samantha Scaramuzza; Alessandro Aiuti; Alessandra Mortellaro
Journal:  Mol Ther       Date:  2020-11-20       Impact factor: 11.454

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