Literature DB >> 18603565

A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease.

Maja Di Rocco1, Fiorina Giona, Francesca Carubbi, Silvia Linari, Fabrizio Minichilli, Roscoe O Brady, Giuliano Mariani, Maria Domenica Cappellini.   

Abstract

BACKGROUND: Gaucher disease is the first lysosomal storage disease for which specific therapy became available. Over 4800 patients have been treated with enzyme replacement therapy. Analysis of Gaucher disease registry data has outlined the clinical heterogeneity of the disease and the different responses to treatment from patient to patient, and for different organs. This variability in clinical response justifies the development of a severity score index to assess disease activity, stage and prognosis, and to quantify the effects of treatment. DESIGN AND METHODS: The new scoring system proposed here, the "Gaucher Disease Severity Score Index - Type I" (GauSSI-I), is based on the clinical experience of the authors and an extensive literature review, including data from the International Gaucher Registry. In particular for skeletal disease, all the available scoring systems have been reviewed and compared in order to provide a skeletal scoring system that allows use of any of the different methods on an equivalent basis.
RESULTS: The new scoring system, GauSSI-I, was developed. Six specific domains, in which different items were scored according to their impact on morbidity, were characterized. GauSSI-I was evaluated in 53 type I Gaucher patients treated with imiglucerase, and it was compared to the Zimran score, the only severity index score so far available.
CONCLUSIONS: The GauSSI-I is a reliable method for staging the severity of adult type I Gaucher disease, and it is more sensitive than the Zimran score for monitoring the response to treatment.

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Year:  2008        PMID: 18603565     DOI: 10.3324/haematol.12379

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  18 in total

1.  Dynamic changes of lipid profile in Romanian patients with Gaucher disease type 1 under enzyme replacement therapy: a prospective study.

Authors:  Anca Zimmermann; Paula Grigorescu-Sido; Heidi Rossmann; Karl J Lackner; Cristina Drugan; Camelia Al Khzouz; Simona Bucerzan; Ioana Naşcu; Tim Zimmermann; Daniel Leucuţa; Matthias M Weber
Journal:  J Inherit Metab Dis       Date:  2012-09-14       Impact factor: 4.982

2.  A disease severity scoring system for children with type 1 Gaucher disease.

Authors:  Staci Kallish; Paige Kaplan
Journal:  Eur J Pediatr       Date:  2012-09-20       Impact factor: 3.183

3.  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

Review 4.  Type 2 Gaucher disease: phenotypic variation and genotypic heterogeneity.

Authors:  N Gupta; I M Oppenheim; E F Kauvar; N Tayebi; E Sidransky
Journal:  Blood Cells Mol Dis       Date:  2010-09-28       Impact factor: 3.039

5.  A reappraisal of Gaucher disease-diagnosis and disease management algorithms.

Authors:  Pramod K Mistry; Maria Domenica Cappellini; Elena Lukina; Hayri Ozsan; Sara Mach Pascual; Hanna Rosenbaum; Maria Helena Solano; Zachary Spigelman; Jesús Villarrubia; Nora Patricia Watman; Gero Massenkeil
Journal:  Am J Hematol       Date:  2011-01       Impact factor: 10.047

6.  Unusual presentation of adult Gaucher's disease: A long and difficult road to diagnosis.

Authors:  Vishakha V Jain; Samir Yelwatkar
Journal:  Indian J Endocrinol Metab       Date:  2011-07

7.  Development and validation of a classification approach for extracting severity automatically from electronic health records.

Authors:  Mary Regina Boland; Nicholas P Tatonetti; George Hripcsak
Journal:  J Biomed Semantics       Date:  2015-04-06

8.  Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3).

Authors:  Neal J Weinreb; David N Finegold; Eleanor Feingold; Zhen Zeng; Barry E Rosenbloom; Suma P Shankar; Dominick Amato
Journal:  Orphanet J Rare Dis       Date:  2015-05-22       Impact factor: 4.123

9.  A phase 2 multi-center, open-label, switch-over trial to evaluate the safety and efficacy of Abcertin® in patients with type 1 Gaucher disease.

Authors:  Jin-Ho Choi; Beom Hee Lee; Jung Min Ko; Young Bae Sohn; Jin-Sung Lee; Gu-Hwan Kim; Sun Hee Heo; June-Young Park; Yoo-Mi Kim; Ja-Hye Kim; Han-Wook Yoo
Journal:  J Korean Med Sci       Date:  2015-03-19       Impact factor: 2.153

Review 10.  Eliglustat tartrate for the treatment of adults with type 1 Gaucher disease.

Authors:  Lunawati L Bennett; Kelsey Turcotte
Journal:  Drug Des Devel Ther       Date:  2015-08-18       Impact factor: 4.162

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