Literature DB >> 24515873

Long-term effectiveness of enzyme replacement therapy in adults with Gaucher disease: results from the NCS-LSD cohort study.

L J Anderson1, W Henley, K M Wyatt, V Nikolaou, D A Hughes, S Waldek, S Logan.   

Abstract

OBJECTIVES: To determine the effectiveness of enzyme replacement therapies (ERT) for adults with Gaucher disease (GD).
DESIGN: A longitudinal, multi-centre cohort study, including prospective and retrospective clinical data. Age- and gender-adjusted treatment effects were estimated using generalised linear mixed models. Treated patients contributed data before and during treatment. Untreated patients contributed natural history data. PARTICIPANTS: Consenting adults (N = 150, aged 16 to 83 years) with a diagnosis of GD who attended a specialist treatment centre in England. At recruitment, 131 patients were receiving ERT (mean treatment duration, 10.8 years; range 0-18 years). OUTCOME MEASURES: Clinical outcomes chosen to reflect disease progression, included platelet count; haemoglobin; absence/presence of bone pain; spleen and liver volumes and AST levels.
RESULTS: One hundred and fifty adults were recruited. Duration of ERT was associated with statistically significant improvements in platelet count (p < 0.001), haemoglobin (p < 0.001), liver and spleen volumes (p < 0.001) and AST levels (p = 0.02).
CONCLUSIONS: These data provide further evidence of the long-term effectiveness of ERT in adults with GD.

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Year:  2014        PMID: 24515873     DOI: 10.1007/s10545-014-9680-0

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


  25 in total

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Authors:  D Elstein; G M Cohn; N Wang; M Djordjevic; C Brutaru; A Zimran
Journal:  Blood Cells Mol Dis       Date:  2010-08-19       Impact factor: 3.039

2.  Evaluation of Gaucher disease using magnetic resonance imaging.

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3.  Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction.

Authors:  Deborah Elstein; A Joseph Foldes; David Zahrieh; Gabriel M Cohn; Maja Djordjevic; Costin Brutaru; Ari Zimran
Journal:  Blood Cells Mol Dis       Date:  2011-05-04       Impact factor: 3.039

4.  Gaucher disease and parkinsonism: a phenotypic and genotypic characterization.

Authors:  N Tayebi; M Callahan; V Madike; B K Stubblefield; E Orvisky; D Krasnewich; J J Fillano; E Sidransky
Journal:  Mol Genet Metab       Date:  2001-08       Impact factor: 4.797

5.  Peripheral neuropathy in adult type 1 Gaucher disease: a 2-year prospective observational study.

Authors:  Marieke Biegstraaten; Eugen Mengel; Laszlo Maródi; Milan Petakov; Claus Niederau; Pilar Giraldo; Derralyn Hughes; Mirando Mrsic; Atul Mehta; Carla E M Hollak; Ivo N van Schaik
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6.  Eight-year clinical outcomes of long-term enzyme replacement therapy for 884 children with Gaucher disease type 1.

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Review 7.  The female Gaucher patient: the impact of enzyme replacement therapy around key reproductive events (menstruation, pregnancy and menopause).

Authors:  Ari Zimran; Elizabeth Morris; Eugen Mengel; Paige Kaplan; Nadia Belmatoug; Derralynn A Hughes; Vera Malinova; Rene Heitner; Elisa Sobreira; Mirando Mrsić; Sorina Granovsky-Grisaru; Dominick Amato; Stephan vom Dahl
Journal:  Blood Cells Mol Dis       Date:  2009-06-06       Impact factor: 3.039

8.  Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources.

Authors:  G A Grabowski; N W Barton; G Pastores; J M Dambrosia; T K Banerjee; M A McKee; C Parker; R Schiffmann; S C Hill; R O Brady
Journal:  Ann Intern Med       Date:  1995-01-01       Impact factor: 25.391

9.  The effectiveness and cost-effectiveness of enzyme and substrate replacement therapies: a longitudinal cohort study of people with lysosomal storage disorders.

Authors:  K Wyatt; W Henley; L Anderson; R Anderson; V Nikolaou; K Stein; L Klinger; D Hughes; S Waldek; R Lachmann; A Mehta; A Vellodi; S Logan
Journal:  Health Technol Assess       Date:  2012       Impact factor: 4.014

10.  THE METABOLISM OF GLUCOCEREBROSIDES. I. PURIFICATION AND PROPERTIES OF A GLUCOCEREBROSIDE-CLEAVING ENZYME FROM SPLEEN TISSUE.

Authors:  R O BRADY; J KANFER; D SHAPIRO
Journal:  J Biol Chem       Date:  1965-01       Impact factor: 5.157

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  3 in total

1.  Long-term effectiveness of enzyme replacement therapy in children with Gaucher disease: results from the NCS-LSD cohort study.

Authors:  L J Anderson; W Henley; K M Wyatt; V Nikolaou; S Waldek; D A Hughes; G M Pastores; S Logan
Journal:  J Inherit Metab Dis       Date:  2014-03-18       Impact factor: 4.982

2.  Case report of unexpected gastrointestinal involvement in type 1 Gaucher disease: comparison of eliglustat tartrate treatment and enzyme replacement therapy.

Authors:  Yoo-Mi Kim; Dong Hoon Shin; Su Bum Park; Chong Kun Cheon; Han-Wook Yoo
Journal:  BMC Med Genet       Date:  2017-05-15       Impact factor: 2.103

3.  A new framework for evaluating the health impacts of treatment for Gaucher disease type 1.

Authors:  Michael L Ganz; Sean Stern; Alex Ward; Luba Nalysnyk; Martin Selzer; Alaa Hamed; Neal Weinreb
Journal:  Orphanet J Rare Dis       Date:  2017-02-20       Impact factor: 4.123

  3 in total

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