Literature DB >> 16846538

Evidence-based recommendations for monitoring bone disease and the response to enzyme replacement therapy in Gaucher patients.

Stephan Vom Dahl1, Ludger Poll, Maja Di Rocco, Giovanni Ciana, Carmencita Denes, Giuliano Mariani, Mario Maas.   

Abstract

BACKGROUND: Bone disease is a serious complication of Gaucher disease. Untreated, it can result in pain, permanent bone damage and disability. Enzyme replacement therapy reverses many of the clinical signs of Gaucher bone disease but early assessment and treatment, and regular monitoring, are essential in optimising outcomes. SCOPE: In September 2005, a group of European experts met to review current knowledge and identify best practice and unmet needs in the monitoring of Gaucher bone disease and the response to enzyme replacement therapy.
METHODS: Medline searches of peer-reviewed literature (no date restrictions) were conducted and supplemented by additional information considered relevant by panellists to furthering discussions. FINDINGS AND
CONCLUSIONS: The group's recommendations included: currently used biochemical bone markers are not clinically practical or reliable; plain X-rays should not be the sole method of assessing bone disease; MRI is the most sensitive method for monitoring bone marrow infiltration by Gaucher cells; semi-quantitative methods for assessing bone marrow infiltration in routine clinical practice should use readily available technology, include an assessment of Gaucher cell infiltration in the lumbar spine and femur, and be validated for inter-rater reliability and in comparison to other methods; a multidisciplinary approach is required for the treatment of Gaucher patients; all Gaucher patients should receive a comprehensive initial radiologic evaluation for bone disease and ongoing radiological monitoring at least once every 2 years.

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Year:  2006        PMID: 16846538     DOI: 10.1185/030079906X104623

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  23 in total

Review 1.  Newborn screening for neuropathic lysosomal storage disorders.

Authors:  Wuh-Liang Hwu; Yin-Hsiu Chien; Ni-Chung Lee
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

Review 2.  Radiological aspects of Gaucher disease.

Authors:  Robert Katz; Tom Booth; Rikin Hargunani; Peter Wylie; Brian Holloway
Journal:  Skeletal Radiol       Date:  2010-07-25       Impact factor: 2.199

Review 3.  Inborn errors of metabolism for the diagnostic radiologist.

Authors:  Chris J Hendriksz
Journal:  Pediatr Radiol       Date:  2008-12-13

Review 4.  Evaluation of an imaging biomarker, Dixon quantitative chemical shift imaging, in Gaucher disease: lessons learned.

Authors:  L van Dussen; E M Akkerman; C E M Hollak; A J Nederveen; M Maas
Journal:  J Inherit Metab Dis       Date:  2014-06-13       Impact factor: 4.982

Review 5.  An overview on bone manifestations in Gaucher disease.

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

6.  Apparent diffusion coefficient of the vertebral bone marrow in children with Gaucher's disease type I and III.

Authors:  Ahmed Abdel Khalek Abdel Razek; Ahmed Abdalla; Abeer Fathy; Ahmed Megahed
Journal:  Skeletal Radiol       Date:  2012-06-21       Impact factor: 2.199

7.  Successful treatment of Gaucher disease type 1 by enzyme replacement therapy over a 10-year duration in a Japanese pediatric patient: A case report.

Authors:  Yuji Oto; Takeshi Inoue; So Nagai; Shinichiro Tanaka; Hisashi Itabashi; Masahisa Shiraisihi; Akihisa Nitta; Nobuyuki Murakami; Hiroyuki Ida; Tomoyo Matsubara
Journal:  Exp Ther Med       Date:  2021-01-22       Impact factor: 2.447

8.  Long-term response in biochemical markers of bone turnover during enzyme replacement therapy in a case-series of patients with Gaucher disease type I from Northern Greece.

Authors:  E Vargiami; M Dimitriadou; M Economou; A Christoforidis; D I Zafeiriou
Journal:  Hippokratia       Date:  2016 Apr-Jun       Impact factor: 0.471

Review 9.  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

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

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