Literature DB >> 14605497

The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement.

T M Cox1, J M F G Aerts, G Andria, M Beck, N Belmatoug, B Bembi, R Chertkoff, S Vom Dahl, D Elstein, A Erikson, M Giralt, R Heitner, C Hollak, M Hrebicek, S Lewis, A Mehta, G M Pastores, A Rolfs, M C Sa Miranda, A Zimran.   

Abstract

N-Butyldeoxynojirimycin (NB-DNJ, miglustat 'Zavesca') is an orally active iminosugar which inhibits the biosynthesis of macromolecular substrates that accumulate pathologically in glycosphingolipidoses. Clinical trials of NB-DNJ in patients with Gaucher's disease demonstrate the therapeutic potential of such substrate inhibitors in the glycolipid storage disorders. However, macrophage-targetted enzyme replacement using intravenous mannose-terminated human glucocerebrosidase (imiglucerase, Cerezyme) is highly effective in ameliorating many of the manifestations of Gaucher's disease and is a treatment in widespread use. Given that imiglucerase and miglustat are now both licensed for the treatment of Gaucher's disease, there is a need to review their therapeutic status. Here the treatment of type 1 (non-neuronopathic) Gaucher disease is evaluated with particular reference to the emerging role of oral N-butyldeoxynojirimycin (miglustat) as a substrate-reducing agent. This position statement represents the consensus viewpoint of an independent international advisory council to the European Working Group on Gaucher Disease.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14605497     DOI: 10.1023/a:1025902113005

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


  41 in total

1.  Quality of life assessment in adults with type 1 Gaucher disease.

Authors:  B J Masek; K B Sims; C M Bove; M S Korson; P Short; D K Norman
Journal:  Qual Life Res       Date:  1999-05       Impact factor: 4.147

Review 2.  Substrate reduction therapy for glycosphingolipid storage disorders.

Authors:  R H Lachmann; F M Platt
Journal:  Expert Opin Investig Drugs       Date:  2001-03       Impact factor: 6.206

3.  The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective study.

Authors:  A M Damiano; G M Pastores; J E Ware
Journal:  Qual Life Res       Date:  1998-07       Impact factor: 4.147

4.  The natural course of Gaucher disease in The Netherlands: implications for monitoring of disease manifestations.

Authors:  P Maaswinkel-Mooij; C Hollak; M van Eysden-Plaisier; M Prins; H Aerts; R Pöll
Journal:  J Inherit Metab Dis       Date:  2000-02       Impact factor: 4.982

5.  Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis.

Authors:  T Cox; R Lachmann; C Hollak; J Aerts; S van Weely; M Hrebícek; F Platt; T Butters; R Dwek; C Moyses; I Gow; D Elstein; A Zimran
Journal:  Lancet       Date:  2000-04-29       Impact factor: 79.321

6.  High prevalence of low serum vitamin B12 in a multi-ethnic Israeli population.

Authors:  Y Gielchinsky; D Elstein; R Green; J W Miller; Y Elstein; N Algur; A Lahad; E Shinar; A Abrahamov; A Zimran
Journal:  Br J Haematol       Date:  2001-12       Impact factor: 6.998

7.  Withdrawal of enzyme replacement therapy in Gaucher's disease.

Authors:  D Elstein; A Abrahamov; I Hadas-Halpern; A Zimran
Journal:  Br J Haematol       Date:  2000-08       Impact factor: 6.998

Review 8.  Gaucher's disease: clinical features and natural history.

Authors:  T M Cox; J P Schofield
Journal:  Baillieres Clin Haematol       Date:  1997-12

9.  N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis.

Authors:  F M Platt; G R Neises; R A Dwek; T D Butters
Journal:  J Biol Chem       Date:  1994-03-18       Impact factor: 5.157

View more
  62 in total

1.  Improved management of lysosomal glucosylceramide levels in a mouse model of type 1 Gaucher disease using enzyme and substrate reduction therapy.

Authors:  John Marshall; Kerry Anne McEachern; Wei-Lien Chuang; Elizabeth Hutto; Craig S Siegel; James A Shayman; Greg A Grabowski; Ronald K Scheule; Diane P Copeland; Seng H Cheng
Journal:  J Inherit Metab Dis       Date:  2010-03-25       Impact factor: 4.982

2.  Isofagomine- and 2,5-anhydro-2,5-imino-D-glucitol-based glucocerebrosidase pharmacological chaperones for Gaucher disease intervention.

Authors:  Zhanqian Yu; Anu R Sawkar; Lisa J Whalen; Chi-Huey Wong; Jeffery W Kelly
Journal:  J Med Chem       Date:  2007-01-11       Impact factor: 7.446

Review 3.  Treatment of lysosomal storage disorders : progress with enzyme replacement therapy.

Authors:  Marianne Rohrbach; Joe T R Clarke
Journal:  Drugs       Date:  2007       Impact factor: 9.546

4.  Neurocognitive testing in late-onset Tay-Sachs disease: a pilot study.

Authors:  D Elstein; G M Doniger; E Simon; I Korn-Lubetzki; R Navon; A Zimran
Journal:  J Inherit Metab Dis       Date:  2008-05-30       Impact factor: 4.982

Review 5.  Clinical neurogenetics: neuropathic lysosomal storage disorders.

Authors:  Gregory M Pastores; Gustavo H B Maegawa
Journal:  Neurol Clin       Date:  2013-11       Impact factor: 3.806

6.  Substrate deprivation therapy in juvenile Sandhoff disease.

Authors:  S B Wortmann; D J Lefeber; G Dekomien; M A A P Willemsen; R A Wevers; E Morava
Journal:  J Inherit Metab Dis       Date:  2009-11-04       Impact factor: 4.982

7.  Glycosphingolipid synthesis inhibition limits osteoclast activation and myeloma bone disease.

Authors:  Adel Ersek; Ke Xu; Aristotelis Antonopoulos; Terry D Butters; Ana Espirito Santo; Youridies Vattakuzhi; Lynn M Williams; Katerina Goudevenou; Lynett Danks; Andrew Freidin; Emmanouil Spanoudakis; Simon Parry; Maria Papaioannou; Evdoxia Hatjiharissi; Aristeidis Chaidos; Dominic S Alonzi; Gabriele Twigg; Ming Hu; Raymond A Dwek; Stuart M Haslam; Irene Roberts; Anne Dell; Amin Rahemtulla; Nicole J Horwood; Anastasios Karadimitris
Journal:  J Clin Invest       Date:  2015-04-27       Impact factor: 14.808

8.  Potential efficacy of enzyme replacement and substrate reduction therapy in three siblings with Gaucher disease type III.

Authors:  J Cox-Brinkman; M J van Breemen; B T van Maldegem; L Bour; W E Donker; C E M Hollak; F A Wijburg; J M F G Aerts
Journal:  J Inherit Metab Dis       Date:  2008-10-15       Impact factor: 4.982

9.  Substrate reduction augments the efficacy of enzyme therapy in a mouse model of Fabry disease.

Authors:  John Marshall; Karen M Ashe; Dinesh Bangari; KerryAnne McEachern; Wei-Lien Chuang; Joshua Pacheco; Diane P Copeland; Robert J Desnick; James A Shayman; Ronald K Scheule; Seng H Cheng
Journal:  PLoS One       Date:  2010-11-24       Impact factor: 3.240

10.  Review of the safety and efficacy of imiglucerase treatment of Gaucher disease.

Authors:  Deborah Elstein; Ari Zimran
Journal:  Biologics       Date:  2009-09-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.