Literature DB >> 26303610

Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity.

A Ahmed1, K Rudser2, A Kunin-Batson3, K Delaney3, C Whitley3, E Shapiro3.   

Abstract

OBJECTIVES: We quantified medical signs and symptoms to construct the Physical Symptom Score (PSS) for use in research to assess somatic disease burden in mucopolysaccharidoses (MPS) to track disease and monitor treatments. We examined scoring reliability, its concurrent validity with other measures, and relationship to age in MPS type I.
METHODS: Fifty-four patients with MPS I (36 with Hurler syndrome treated with hematopoietic cell transplant and 18 with attenuated MPS I treated with enzyme replacement therapy), ages 5 to 18 years, were seen longitudinally over 5 years. The summation of frequency and severity of signs of specific organ involvement, surgeries, and hydrocephalus drawn from medical histories comprise the PSS. We examined relationship to age and to daily living skills (DLS) from the Vineland Adaptive Behavior Scale and physical quality of life from the Child Health Questionnaire (CHQ) for each group.
RESULTS: The PSS was associated with age in both groups, indicating increase in disease burden over time. The PSS was significantly negatively associated with DLS (r = -0.48) and CHQ (r = -0.55) in the attenuated MPS I but not in the Hurler group.
CONCLUSIONS: The association of somatic disease burden with physical quality of life and ability to carry out daily living skills suggests that the PSS will be useful in the measurement of disease and treatment effects in the attenuated MPS I group. Earlier treatment with transplant and differing parental expectations are possible explanations for its lack of association with other outcomes necessitating an adaptation for Hurler syndrome in the future.

Entities:  

Year:  2015        PMID: 26303610      PMCID: PMC4864710          DOI: 10.1007/8904_2015_485

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  19 in total

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2.  The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type I.

Authors:  Gregory M Pastores; Pamela Arn; Michael Beck; Joe T R Clarke; Nathalie Guffon; Paige Kaplan; Joseph Muenzer; Denise Y J Norato; Elsa Shapiro; Janet Thomas; David Viskochil; J Edmond Wraith
Journal:  Mol Genet Metab       Date:  2007-03-02       Impact factor: 4.797

3.  Cognitive, medical, and neuroimaging characteristics of attenuated mucopolysaccharidosis type II.

Authors:  Brianna Yund; Kyle Rudser; Alia Ahmed; Victor Kovac; Igor Nestrasil; Julian Raiman; Eva Mamak; Paul Harmatz; Robert Steiner; Heather Lau; Pooja Vekaria; Jeffrey R Wozniak; Kelvin O Lim; Kathleen Delaney; Chester Whitley; Elsa G Shapiro
Journal:  Mol Genet Metab       Date:  2014-12-09       Impact factor: 4.797

4.  IDUA mutational profiling of a cohort of 102 European patients with mucopolysaccharidosis type I: identification and characterization of 35 novel α-L-iduronidase (IDUA) alleles.

Authors:  Francesca Bertola; Mirella Filocamo; Giorgio Casati; Matthew Mort; Camillo Rosano; Anna Tylki-Szymanska; Beyhan Tüysüz; Orazio Gabrielli; Serena Grossi; Maurizio Scarpa; Giancarlo Parenti; Daniela Antuzzi; Jaime Dalmau; Maja Di Rocco; Carlo Dionisi Vici; Ilyas Okur; Jordi Rosell; Attilio Rovelli; Francesca Furlan; Miriam Rigoldi; Andrea Biondi; David N Cooper; Rossella Parini
Journal:  Hum Mutat       Date:  2011-03-10       Impact factor: 4.878

Review 5.  Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

Authors:  H S Scott; S Bunge; A Gal; L A Clarke; C P Morris; J J Hopwood
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6.  Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase).

Authors:  James E Wraith; Lorne A Clarke; Michael Beck; Edwin H Kolodny; Gregory M Pastores; Joseph Muenzer; David M Rapoport; Kenneth I Berger; Stuart J Swiedler; Emil D Kakkis; Tanja Braakman; Elenie Chadbourne; Karen Walton-Bowen; Gerald F Cox
Journal:  J Pediatr       Date:  2004-05       Impact factor: 4.406

7.  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

8.  Prevalence of lysosomal storage disorders.

Authors:  P J Meikle; J J Hopwood; A E Clague; W F Carey
Journal:  JAMA       Date:  1999-01-20       Impact factor: 56.272

9.  Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry.

Authors:  Kristin D'Aco; Lisa Underhill; Lakshmi Rangachari; Pamela Arn; Gerald F Cox; Roberto Giugliani; Torayuki Okuyama; Frits Wijburg; Paige Kaplan
Journal:  Eur J Pediatr       Date:  2012-01-11       Impact factor: 3.183

10.  The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK.

Authors:  David Moore; Martin J Connock; Ed Wraith; Christine Lavery
Journal:  Orphanet J Rare Dis       Date:  2008-09-16       Impact factor: 4.123

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  5 in total

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2.  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
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3.  In utero adenine base editing corrects multi-organ pathology in a lethal lysosomal storage disease.

Authors:  Sourav K Bose; Brandon M White; Meghana V Kashyap; Apeksha Dave; Felix R De Bie; Haiying Li; Kshitiz Singh; Pallavi Menon; Tiankun Wang; Shiva Teerdhala; Vishal Swaminathan; Heather A Hartman; Sowmya Jayachandran; Prashant Chandrasekaran; Kiran Musunuru; Rajan Jain; David B Frank; Philip Zoltick; William H Peranteau
Journal:  Nat Commun       Date:  2021-07-13       Impact factor: 14.919

4.  Association of somatic burden of disease with age and neuropsychological measures in attenuated mucopolysaccharidosis types I, II and VI.

Authors:  Alia Ahmed; Elsa Shapiro; Kyle Rudser; Alicia Kunin-Batson; Kelly King; Chester B Whitley
Journal:  Mol Genet Metab Rep       Date:  2016-04-01

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

Authors:  Elsa G Shapiro; Chester B Whitley; Julie B Eisengart
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