Please use this identifier to cite or link to this item:
Scopus Web of Science® Altmetric
Type: Journal article
Title: Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Author: Harmatz, P.
Yu, Z.
Giugliani, R.
Schwartz, I.
Guffon, N.
Teles, E.
Miranda, C.
Wraith, J.
Beck, M.
Arash, L.
Scarpa, M.
Ketteridge, D.
Hopwood, J.
Plecko, B.
Steiner, R.
Whitley, C.
Kaplan, P.
Swiedler, S.
Hardy, K.
Berger, K.
et al.
Citation: Journal of Inherited Metabolic Disease, 2010; 33(1):51-60
Publisher: Kluwer Academic Publ
Issue Date: 2010
ISSN: 0141-8955
Statement of
Paul Harmatz... John J. Hopwood... et al.
Abstract: Pulmonary function is impaired in untreated mucopolysaccharidosis type VI (MPS VI). Pulmonary function was studied in patients during long-term enzyme replacement therapy (ERT) with recombinant human arylsulfatase B (rhASB; rhN-acetylgalactosamine 4-sulfatase). Pulmonary function tests prior to and for up to 240 weeks of weekly infusions of rhASB at 1 mg/kg were completed in 56 patients during Phase 1/2, Phase 2, Phase 3 and Phase 3 Extension trials of rhASB and the Survey Study. Forced vital capacity (FVC), forced expiratory volume in 1 s (FEV1) and, in a subset of patients, maximum voluntary ventilation (MVV), were analyzed as absolute volume in liters. FEV1 and FVC showed little change from baseline during the first 24 weeks of ERT, but after 96 weeks, these parameters increased over baseline by 11% and 17%, respectively. This positive trend compared with baseline continued beyond 96 weeks of treatment. Improvements from baseline in pulmonary function occurred along with gains in height in the younger group (5.5% change) and in the older patient group (2.4% change) at 96 weeks. Changes in MVV occurred earlier within 24 weeks of treatment to approximately 15% over baseline. Model results based on data from all trials showed significant improvements in the rate of change in pulmonary function during 96 weeks on ERT, whereas little or no improvement was observed for the same time period prior to ERT. Thus, analysis of mean percent change data and longitudinal modeling both indicate that long-term ERT resulted in improvement in pulmonary function in MPS VI patients.
Keywords: Lung
Mucopolysaccharidosis VI
Recombinant Proteins
Respiratory Function Tests
Longitudinal Studies
Cross-Sectional Studies
Double-Blind Method
Research Design
Child, Preschool
Rights: © The Author(s) 2010. This article is published with open access at This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
DOI: 10.1007/s10545-009-9007-8
Appears in Collections:Aurora harvest 5
Paediatrics publications

Files in This Item:
File Description SizeFormat 
hdl_63363.pdfPublished version178.49 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.