Literature DB >> 23512580

Plasmatic kinetics of dermatan sulfate during enzyme replacement therapy with iduronate-2-sulfatase in a mucopolysaccharidosis II patient.

Nicola Volpi1, Lucia Zampini, Francesca Maccari, Lucia Santoro, Fabio Galeotti, Tiziana Galeazzi, Orazio Gabrielli, Giovanni V Coppa.   

Abstract

Enzyme replacement therapy (ERT) is the worldwide standard of care for a number of mucopolysaccharidosis (MPS) diseases. We report a kinetic study of plasmatic dermatan sulfate (DS) in a 3-year-old subject affected by a severe form of MPS II during the first 10 months of ERT with Idursulfase. A strong increase in the DS plasmatic concentration was measured immediately after the first enzyme infusion, with a maximum after 3 h, followed by a continuous decrease in the 8-15 days following the beginning of treatment. After this, a constant plasmatic content of DS concentration was observed. Overall, during the 10-month treatment period, ERT reduced the plasmatic concentration of DS up to ~80-85 %, but it was unable to totally remove it from the blood. We can suppose that immediately after the first enzyme administrations, a large amount of abnormal DS is removed from tissues reaching the blood compartment and eliminated via the urine, and thereafter only minimal changes are observed. The persistency of the residual amounts of DS with the actually recommended dosage in our Patient may suggest the opportunity to promote further studies with increased enzyme dosages to completely remove the accumulation of lysosomal DS.

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Year:  2013        PMID: 23512580     DOI: 10.1007/s10719-013-9471-0

Source DB:  PubMed          Journal:  Glycoconj J        ISSN: 0282-0080            Impact factor:   2.916


  17 in total

1.  Effect of 6 years of enzyme replacement therapy on plasma and urine glycosaminoglycans in attenuated MPS I patients.

Authors:  Giovanni V Coppa; Dania Buzzega; Lucia Zampini; Francesca Maccari; Tiziana Galeazzi; Francesca Pederzoli; Orazio Gabrielli; Nicola Volpi
Journal:  Glycobiology       Date:  2010-06-09       Impact factor: 4.313

Review 2.  Enzyme replacement therapy for the management of the mucopolysaccharidoses.

Authors:  J E Wraith
Journal:  Int J Clin Pharmacol Ther       Date:  2009       Impact factor: 1.366

3.  Disease-specific markers for the mucopolysaccharidoses.

Authors:  Maria Fuller; Tina Rozaklis; Steven L Ramsay; John J Hopwood; Peter J Meikle
Journal:  Pediatr Res       Date:  2004-09-03       Impact factor: 3.756

4.  Clinical application of a new simple method for the identification of mucopolysaccharidoses.

Authors:  G V Coppa; C Catassi; O Gabrielli; P L Giorgi; R Dall'Amico; S Naia; G Panin; L Chiandetti
Journal:  Helv Paediatr Acta       Date:  1987-06

5.  Isolation and characterization of undersulphated chondroitin-4-sulphate from normal human plasma.

Authors:  M Juvani; C Friman; H Ranta; O Wegelius
Journal:  Biochim Biophys Acta       Date:  1975-11-10

Review 6.  High-performance liquid chromatographic analysis of glycosaminoglycan-derived oligosaccharides.

Authors:  T Imanari; T Toida; I Koshiishi; H Toyoda
Journal:  J Chromatogr A       Date:  1996-01-12       Impact factor: 4.759

Review 7.  Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

Authors:  Rick Martin; Michael Beck; Christine Eng; Roberto Giugliani; Paul Harmatz; Verónica Muñoz; Joseph Muenzer
Journal:  Pediatrics       Date:  2008-02       Impact factor: 7.124

8.  Structural analysis of bikunin glycosaminoglycan.

Authors:  Lianli Chi; Jeremy J Wolff; Tatiana N Laremore; Odile F Restaino; Jin Xie; Chiara Schiraldi; Toshihiko Toida; I Jonathan Amster; Robert J Linhardt
Journal:  J Am Chem Soc       Date:  2008-02-05       Impact factor: 15.419

9.  Idursulfase treatment of Hunter syndrome in children younger than 6 years: results from the Hunter Outcome Survey.

Authors:  Joseph Muenzer; Michael Beck; Roberto Giugliani; Yasuyuki Suzuki; Anna Tylki-Szymanska; Vassili Valayannopoulos; Ashok Vellodi; James E Wraith
Journal:  Genet Med       Date:  2011-02       Impact factor: 8.822

10.  A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome).

Authors:  Joseph Muenzer; James E Wraith; Michael Beck; Roberto Giugliani; Paul Harmatz; Christine M Eng; Ashok Vellodi; Rick Martin; Uma Ramaswami; Muge Gucsavas-Calikoglu; Suresh Vijayaraghavan; Susanne Wendt; Suzanne Wendt; Ana Cristina Puga; Antonio Puga; Brian Ulbrich; Marwan Shinawi; Maureen Cleary; Diane Piper; Anne Marie Conway; Ann Marie Conway; Alan Kimura
Journal:  Genet Med       Date:  2006-08       Impact factor: 8.822

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  1 in total

1.  The Value of Case Reports in Systematic Reviews from Rare Diseases. The Example of Enzyme Replacement Therapy (ERT) in Patients with Mucopolysaccharidosis Type II (MPS-II).

Authors:  Miguel Sampayo-Cordero; Bernat Miguel-Huguet; Andrea Malfettone; José Manuel Pérez-García; Antonio Llombart-Cussac; Javier Cortés; Almudena Pardo; Jordi Pérez-López
Journal:  Int J Environ Res Public Health       Date:  2020-09-10       Impact factor: 3.390

  1 in total

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