Literature DB >> 15490271

Bone density changes with enzyme therapy for Gaucher disease.

Ehud Lebel1, Altoon Dweck, A Joseph Foldes, Yosef Golowa, Menachem Itzchaki, Ari Zimran, Deborah Elstein.   

Abstract

Gaucher disease is the most common lysosomal storage disease. Enzyme replacement therapy engenders improvement in hematological and visceral parameters; however, improvement in bone density (BMD) with treatment has not been confirmed. This study presents follow-up of BMD in the first ten patients in Israel treated with low-dose recombinant enzyme for up to 108 months. BMD at femoral neck and lumbar spine was determined by dual-energy X-ray absorptiometry (DEXA) at the start of the trial, after 3-6 months, after 18-24 months, and at the most recent follow-up. BMD in all patients was very low at onset and never normalized. There was a decrease in BMD in all patients at 3-6 months. Older patients (four women, two men; >30 years of age) showed some improvement in BMD during treatment. Younger patients (four females; 18-23 years of age) did not show a statistically significant improvement. These findings might reflect the failure of patients with Gaucher disease to achieve expected peak bone density at appropriate chronological milestones despite treatment. Nonetheless, the z-scores of the older patients were better than those of the younger patients, implying some catch-up period. Yet, some patients with Gaucher disease evince rapid onset of osteoporosis in early adulthood. Enzyme treatment per se, as well as attendant improved well-being and increased physical activity, may induce amelioration in BMD at this later stage. One may consider adding anti-osteoporosis therapy in young adults to induce earlier "catch up" to peak bone mass, and then enzyme replacement in later adulthood to prevent decrements in bone mass related to Gaucher cell infiltration. Copyright 2004 Springer-Verlag

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Year:  2004        PMID: 15490271     DOI: 10.1007/s00774-004-0529-8

Source DB:  PubMed          Journal:  J Bone Miner Metab        ISSN: 0914-8779            Impact factor:   2.626


  10 in total

Review 1.  Gaucher disease: a systematic review and meta-analysis of bone complications and their response to treatment.

Authors:  Siavash Piran; Dominick Amato
Journal:  J Inherit Metab Dis       Date:  2010-03-25       Impact factor: 4.982

2.  Vertebral fractures in Gaucher disease type I: data from the French "Observatoire" on Gaucher disease (FROG).

Authors:  R-M Javier; E Hachulla; C Rose; V Gressin; P Chérin; E Noël; C de Roux-Serratrice; D Dobbelaere; A Hartmann; R Jaussaud; P Clerson; B Grosbois; C Roux
Journal:  Osteoporos Int       Date:  2010-08-04       Impact factor: 4.507

3.  The pharmacological chaperone isofagomine increases the activity of the Gaucher disease L444P mutant form of beta-glucosidase.

Authors:  Richie Khanna; Elfrida R Benjamin; Lee Pellegrino; Adriane Schilling; Brigitte A Rigat; Rebecca Soska; Hadis Nafar; Brian E Ranes; Jessie Feng; Yi Lun; Allan C Powe; David J Palling; Brandon A Wustman; Raphael Schiffmann; Don J Mahuran; David J Lockhart; Kenneth J Valenzano
Journal:  FEBS J       Date:  2010-02-10       Impact factor: 5.542

Review 4.  An overview on bone manifestations in Gaucher disease.

Authors:  Peter Mikosch; Derralynn Hughes
Journal:  Wien Med Wochenschr       Date:  2010-12

5.  Type 1 Gaucher disease: significant disease manifestations in "asymptomatic" homozygotes.

Authors:  Manisha Balwani; Laura Fuerstman; Ruth Kornreich; Lisa Edelmann; Robert J Desnick
Journal:  Arch Intern Med       Date:  2010-09-13

Review 6.  Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring.

Authors:  T M Cox; J M F G Aerts; N Belmatoug; M D Cappellini; S vom Dahl; J Goldblatt; G A Grabowski; C E M Hollak; P Hwu; M Maas; A M Martins; P K Mistry; G M Pastores; A Tylki-Szymanska; J Yee; N Weinreb
Journal:  J Inherit Metab Dis       Date:  2008-05-23       Impact factor: 4.982

7.  Skeletal involvement in Gaucher disease: extent of bone disease, splenic volume, and quality of life.

Authors:  Ricardo Andrade Fernandes de Mello; Melissa Bosi Nonato Mello; Laís Bastos Pessanha; Ana Paula Alves Fonseca
Journal:  Radiol Bras       Date:  2021 Mar-Apr

8.  Improvement in bone marrow infiltration in patients with type I Gaucher disease treated with taliglucerase alfa.

Authors:  Ari Zimran; Tama Dinur; Shoshana Revel-Vilk; Eric M Akkerman; Laura van Dussen; Carla E M Hollak; Hannah Maayan; Gheona Altarescu; Raul Chertkoff; Mario Maas
Journal:  J Inherit Metab Dis       Date:  2018-07-31       Impact factor: 4.982

Review 9.  Imiglucerase in the treatment of Gaucher disease: a history and perspective.

Authors:  Patrick B Deegan; Timothy M Cox
Journal:  Drug Des Devel Ther       Date:  2012-04-18       Impact factor: 4.162

10.  Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study.

Authors:  K B Sims; G M Pastores; N J Weinreb; J Barranger; B E Rosenbloom; S Packman; P Kaplan; H Mankin; R Xavier; J Angell; M A Fitzpatrick; D Rosenthal
Journal:  Clin Genet       Date:  2008-02-27       Impact factor: 4.438

  10 in total

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