Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7795
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Type: Journal article
Title: Disease-specific markers for the mucopolysaccharidoses
Author: Fuller, M.
Rozaklis, T.
Ramsay, S.
Hopwood, J.
Meikle, P.
Citation: Pediatric Research, 2004; 56(5):733-738
Publisher: Int Pediatric Research Foundation Inc
Issue Date: 2004
ISSN: 0031-3998
1530-0447
Statement of
Responsibility: 
Maria Fuller, Tina Rozaklis, Steven L Ramsay, John J Hopwood, and Peter J Meikle
Abstract: Unprecedented demands are now placed on clinicians for early diagnosis as we enter into an era of advancing treatment opportunities for the mucopolysaccharidoses (MPS). Biochemical monitoring of any therapeutic avenue will also be prerequisite. To this end, we aimed to identify a range of urinary oligosaccharides that could be used to identify and characterize patients with MPS. We analyzed 94 urine samples from 68 patients with MPS and 26 control individuals for oligosaccharides derived from glycosaminoglycans using electrospray ionization-tandem mass spectrometry. The oligosaccharide profile for each patient group was compared with that of the control group. The Mann-Whitney U test was used to measure the difference between each patient group and the controls for each analyte. Urine samples from patients before and at successive times after bone marrow transplantation were also evaluated. A number of oligosaccharides were identified in the urine of each MPS subtype, and for each of these, specific oligosaccharide profiles were formulated. These profiles enabled the identification of all 68 patients and their subtypes with the exception of MPS IIIB and IIIC. Selected oligosaccharides were used to assess three individuals after a bone marrow transplant, and, in each case, a substantial reduction in the level of diagnostic oligosaccharides, posttransplantation, was observed. The identification and measurement of glycosaminoglycan-derived oligosaccharides in urine provides a sensitive and specific screen for the early identification of individuals with MPS. The resulting oligosaccharide profiles not only characterize subtype but also provide a disease-specific fingerprint for the biochemical monitoring of current and proposed therapies.
Keywords: Humans; Mucopolysaccharidoses; Oligosaccharides; Biological Markers; Spectrometry, Mass, Electrospray Ionization; Carbohydrate Sequence; Molecular Sequence Data
Rights: Copyright © 2004 International Pediatric Research
RMID: 0020041080
DOI: 10.1203/01.PDR.0000141987.69757.DD
Appears in Collections:Paediatrics publications

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