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

被引:181
作者
Cox, TM
Aerts, JMFG
Andria, G
Beck, M
Belmatoug, N
Bembi, B
Chertkoff, R
Vom Dahl, S
Elstein, D
Erikson, A
Giralt, M
Heitner, R
Hollak, C
Hrebicek, M
Lewis, S
Mehta, A
Pastores, GM
Rolfs, A
Miranda, MCS
Zimran, A
机构
[1] Univ Cambridge, Addenbrookes Hosp, Dept Med, Cambridge CB2 2QQ, England
[2] Univ Amsterdam, Acad Med Ctr, Dept Biochem, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Naples Federico II, Dept Paediat, Naples, Italy
[4] Johannes Gutenberg Univ Mainz, Kinderklin, Biochem Genet Lab, D-6500 Mainz, Germany
[5] Hop Beaujon, Clichy, France
[6] Ist Infanzia Burlo Garofolo, Trieste, Italy
[7] Israeli Gaucher Patients Assoc, Haifa, Israel
[8] Univ Dusseldorf, Univ Klinikum, Klin Gastroenterol Hepatol & Infektiol, D-4000 Dusseldorf, Germany
[9] Shaare Zedek Med Ctr, Gaucher Clin, Jerusalem, Israel
[10] Univ Umea Hosp, Dept Paediat, S-90185 Umea, Sweden
[11] Hosp Miguel Servet, Serv Hematol, Zaragoza, Spain
[12] Univ Witwatersrand, Johannesburg Hosp, Dept Paediat, Gaucher Clin, ZA-2050 Johannesburg, South Africa
[13] Univ Amsterdam, Acad Med Ctr, Dept Internal Med & Haematol, NL-1105 AZ Amsterdam, Netherlands
[14] Inst Inherited Metab Disorders, Prague, Czech Republic
[15] Gauchers Assoc, London, England
[16] Royal Free Hosp, Dept Haematol, London NW3 2QG, England
[17] NYU, Sch Med, New York, NY USA
[18] Univ Rostock, Neurol Klin & Poliklin, Rostock, Germany
[19] Inst Med Genet, Oporto, Portugal
[20] Shaare Zedek Med Ctr, Dept Med, Gaucher Clin, IL-91000 Jerusalem, Israel
关键词
D O I
10.1023/A:1025902113005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
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收藏
页码:513 / 526
页数:14
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