Literature DB >> 22991166

Plasma and urinary levels of dermatan sulfate and heparan sulfate derived disaccharides after long-term enzyme replacement therapy (ERT) in MPS I: correlation with the timing of ERT and with total urinary excretion of glycosaminoglycans.

Minke H de Ru1, Linda van der Tol, Naomi van Vlies, Brian W Bigger, Carla E M Hollak, Lodewijk Ijlst, Wim Kulik, Henk van Lenthe, Muhammad A Saif, Tom Wagemans, Willem M van der Wal, Ronald J Wanders, Frits A Wijburg.   

Abstract

INTRODUCTION: Mucopolysaccharidosis type I (MPS I) results in a defective breakdown of the glycosaminoglycans (GAGs) heparan sulfate and dermatan sulfate, which leads to a progressive disease. Enzyme replacement therapy (ERT) results in clearance of these GAGs from a range of tissues and can significantly ameliorate several symptoms. The biochemical efficacy of ERT is generally assessed by the determination of the total urinary excretion of GAGs. However, this has limitations. We studied the concentrations of heparan sulfate and dermatan sulfate derived disaccharides (HS and DS, respectively) in the plasma and urine of seven patients and compared these levels with total urinary GAGs (uGAGs) levels.
METHODS: Plasma and urine samples were collected at different time points relative to the weekly ERT for three non-consecutive weeks in seven MPS I patients who had been treated with ERT for at least 2.5 years. Heparan and dermatan sulfate in plasma and urine were enzymatically digested into disaccharides, and HS and DS levels were determined by HPLC-MS/MS analysis. uGAGs were measured by the DMB test.
RESULTS: The levels of HS and DS were markedly decreased compared with the levels before the initiation of ERT. However, the concentrations of DS in plasma and of both HS and DS in urine remained significantly elevated in all studied patients, while in six patients the level of total uGAGs had normalized. The concentrations of plasma and urinary HS during the weekly ERT followed a U-shaped curve. However, the effect size is small. The concentrations of plasma and urinary DS and uGAGs appeared to be in a steady state.
CONCLUSIONS: HS and DS are sensitive biomarkers for monitoring the biochemical treatment efficacy of ERT and remain elevated despite long-term treatment. This finding may be related to the labeled dose or antibody status of the patient. The timing of the sample collection is not relevant, at least at the current dose of 100 IU/kg/weekly.

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Year:  2012        PMID: 22991166     DOI: 10.1007/s10545-012-9538-2

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  24 in total

1.  Hematopoietic stem cell transplantation improves the high incidence of neutralizing allo-antibodies observed in Hurler's syndrome after pharmacological enzyme replacement therapy.

Authors:  Muhammad Ameer Saif; Brian W Bigger; Karen E Brookes; Jean Mercer; Karen L Tylee; Heather J Church; Denise K Bonney; Simon Jones; J Ed Wraith; Robert F Wynn
Journal:  Haematologica       Date:  2012-02-27       Impact factor: 9.941

2.  Biochemical monitoring after haemopoietic stem cell transplant for Hurler syndrome (MPSIH): implications for functional outcome after transplant in metabolic disease.

Authors:  H Church; K Tylee; A Cooper; M Thornley; J Mercer; E Wraith; T Carr; A O'Meara; R F Wynn
Journal:  Bone Marrow Transplant       Date:  2007-01-15       Impact factor: 5.483

3.  Disaccharide structure code for the easy representation of constituent oligosaccharides from glycosaminoglycans.

Authors:  Roger Lawrence; Hong Lu; Robert D Rosenberg; Jeffrey D Esko; Lijuan Zhang
Journal:  Nat Methods       Date:  2008-04       Impact factor: 28.547

4.  Longitudinal observations of serum heparin cofactor II-thrombin complex in treated Mucopolysaccharidosis I and II patients.

Authors:  Lorne Andrew Clarke; Harmony Hemmelgarn; Karen Colobong; Anita Thomas; Sylvia Stockler; Robin Casey; Alicia Chan; Paul Fernoff; John Mitchell
Journal:  J Inherit Metab Dis       Date:  2011-07-06       Impact factor: 4.982

5.  A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years.

Authors:  Monica Sifuentes; Robin Doroshow; Richard Hoft; Greg Mason; Irwin Walot; Michael Diament; Susan Okazaki; Kenneth Huff; Gerald F Cox; Stuart J Swiedler; Emil D Kakkis
Journal:  Mol Genet Metab       Date:  2006-09-29       Impact factor: 4.797

6.  Dimethylmethylene blue-based spectrophotometry of glycosaminoglycans in untreated urine: a rapid screening procedure for mucopolysaccharidoses.

Authors:  J G de Jong; R A Wevers; C Laarakkers; B J Poorthuis
Journal:  Clin Chem       Date:  1989-07       Impact factor: 8.327

7.  Recombinant expression, purification, and kinetic characterization of chondroitinase AC and chondroitinase B from Flavobacterium heparinum.

Authors:  K Pojasek; Z Shriver; P Kiley; G Venkataraman; R Sasisekharan
Journal:  Biochem Biophys Res Commun       Date:  2001-08-17       Impact factor: 3.575

8.  Evaluation of heparin cofactor II-thrombin complex as a biomarker on blood spots from mucopolysaccharidosis I, IIIA and IIIB mice.

Authors:  Kia Langford-Smith; Malani Arasaradnam; J Ed Wraith; Rob Wynn; Brian W Bigger
Journal:  Mol Genet Metab       Date:  2009-10-23       Impact factor: 4.797

9.  Improved metabolic correction in patients with lysosomal storage disease treated with hematopoietic stem cell transplant compared with enzyme replacement therapy.

Authors:  Robert F Wynn; J Ed Wraith; Jean Mercer; Anne O'Meara; Karen Tylee; Margaret Thornley; Heather J Church; Brian W Bigger
Journal:  J Pediatr       Date:  2009-04       Impact factor: 4.406

10.  Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

Authors:  Lorne A Clarke; J Edmond Wraith; Michael Beck; Edwin H Kolodny; Gregory M Pastores; Joseph Muenzer; David M Rapoport; Kenneth I Berger; Marisa Sidman; Emil D Kakkis; Gerald F Cox
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

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  26 in total

1.  Chondroitin 6-Sulfate as a Novel Biomarker for Mucopolysaccharidosis IVA and VII.

Authors:  Tsutomu Shimada; Shunji Tomatsu; Eriko Yasuda; Robert W Mason; William G Mackenzie; Yuniko Shibata; Francyne Kubaski; Roberto Giugliani; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii
Journal:  JIMD Rep       Date:  2014-05-22

2.  Early Umbilical Cord Blood-Derived Stem Cell Transplantation Does Not Prevent Neurological Deterioration in Mucopolysaccharidosis Type III.

Authors:  Lindsey Welling; Jan Pieter Marchal; Peter van Hasselt; Ans T van der Ploeg; Frits A Wijburg; Jaap Jan Boelens
Journal:  JIMD Rep       Date:  2014-09-26

3.  The circulating glycosaminoglycan signature of respiratory failure in critically ill adults.

Authors:  Eric P Schmidt; Guoyun Li; Lingyun Li; Li Fu; Yimu Yang; Katherine H Overdier; Ivor S Douglas; Robert J Linhardt
Journal:  J Biol Chem       Date:  2014-02-07       Impact factor: 5.157

4.  Newborn screening and diagnosis of mucopolysaccharidoses: application of tandem mass spectrometry.

Authors:  Shunji Tomatsu; Francyne Kubaski; Kazuki Sawamoto; Robert W Mason; Eriko Yasuda; Tsutomu Shimada; Adriana M Montaño; Seiji Yamaguchi; Yasuyuki Suzuki; Tadao Orii
Journal:  Nihon Masu Sukuriningu Gakkai Shi       Date:  2014

5.  Adverse Effects of Genistein in a Mucopolysaccharidosis Type I Mouse Model.

Authors:  Sandra D K Kingma; Tom Wagemans; Lodewijk IJlst; Jurgen Seppen; Marion J J Gijbels; Frits A Wijburg; Naomi van Vlies
Journal:  JIMD Rep       Date:  2015-04-09

Review 6.  Enzyme replacement therapy for mucopolysaccharidoses; past, present, and future.

Authors:  Hui Hsuan Chen; Kazuki Sawamoto; Robert W Mason; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Shunji Tomatsu
Journal:  J Hum Genet       Date:  2019-08-27       Impact factor: 3.172

Review 7.  Contribution of tandem mass spectrometry to the diagnosis of lysosomal storage disorders.

Authors:  Monique Piraud; Magali Pettazzoni; Pamela Lavoie; Séverine Ruet; Cécile Pagan; David Cheillan; Philippe Latour; Christine Vianey-Saban; Christiane Auray-Blais; Roseline Froissart
Journal:  J Inherit Metab Dis       Date:  2018-03-19       Impact factor: 4.982

8.  Novel heparan sulfate assay by using automated high-throughput mass spectrometry: Application to monitoring and screening for mucopolysaccharidoses.

Authors:  Tsutomu Shimada; Joan Kelly; William A LaMarr; Naomi van Vlies; Eriko Yasuda; Robert W Mason; William Mackenzie; Francyne Kubaski; Roberto Giugliani; Yasutsugu Chinen; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji E Orii; Toshiyuki Fukao; Tadao Orii; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2014-07-21       Impact factor: 4.797

Review 9.  Newborn screening and diagnosis of mucopolysaccharidoses.

Authors:  Shunji Tomatsu; Tadashi Fujii; Masaru Fukushi; Toshihiro Oguma; Tsutomu Shimada; Miho Maeda; Kazuhiro Kida; Yuniko Shibata; Hideyuki Futatsumori; Adriana M Montaño; Robert W Mason; Seiji Yamaguchi; Yasuyuki Suzuki; Tadao Orii
Journal:  Mol Genet Metab       Date:  2013-06-21       Impact factor: 4.797

Review 10.  Molecular genetics and metabolism, special edition: Diagnosis, diagnosis and prognosis of Mucopolysaccharidosis IVA.

Authors:  Hira Peracha; Kazuki Sawamoto; Lauren Averill; Heidi Kecskemethy; Mary Theroux; Mihir Thacker; Kyoko Nagao; Christian Pizarro; William Mackenzie; Hironori Kobayashi; Seiji Yamaguchi; Yasuyuki Suzuki; Kenji Orii; Tadao Orii; Toshiyuki Fukao; Shunji Tomatsu
Journal:  Mol Genet Metab       Date:  2018-05-15       Impact factor: 4.797

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