Literature DB >> 26096742

Long-term treatment outcomes in Gaucher disease.

Joel Charrow1,2, C Ronald Scott3.   

Abstract

Following the treatment of the first Gaucher disease patient with enzyme replacement therapy (ERT), it was clear that ERT had the potential to be transformative with dramatic improvements in systemic manifestations of the disease within 2 years. Following over 20 years existence of the International Collaborative Gaucher Group Gaucher Registry and evidence from ∼6000 patients, the long-term effects of therapy have been documented. It has been shown that ERT can result in improvements in all clinical and laboratory parameters of nonneuronopathic disease. However, different aspects of the disease, such as hematologic parameters, organ volumes and bone disease do not necessarily respond to therapy at the same rate or to the same extent, and this has had major implications for disease monitoring and for the establishment of therapeutic goals for ERT. Response may be affected by factors such as the timing of therapy initiation, the presence of irreversible complications such as osteonecrosis, and by enzyme dose. It is also apparent that ERT has no impact on neurological aspects of disease and highlights the need for additional or alternative treatment strategies able to meet the needs of patients with neuronopathic disease.
© 2015 Wiley Periodicals, Inc.

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Year:  2015        PMID: 26096742     DOI: 10.1002/ajh.24056

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  15 in total

1.  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

2.  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.  Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data.

Authors:  Tatiana Raskovalova; Patrick B Deegan; Ruby Yang; Elena Pavlova; Jérome Stirnemann; José Labarère; Ari Zimran; Pramod K Mistry; Marc Berger
Journal:  Syst Rev       Date:  2017-04-20

Review 4.  A Review of Gaucher Disease Pathophysiology, Clinical Presentation and Treatments.

Authors:  Jérôme Stirnemann; Nadia Belmatoug; Fabrice Camou; Christine Serratrice; Roseline Froissart; Catherine Caillaud; Thierry Levade; Leonardo Astudillo; Jacques Serratrice; Anaïs Brassier; Christian Rose; Thierry Billette de Villemeur; Marc G Berger
Journal:  Int J Mol Sci       Date:  2017-02-17       Impact factor: 5.923

5.  Transformation in pretreatment manifestations of Gaucher disease type 1 during two decades of alglucerase/imiglucerase enzyme replacement therapy in the International Collaborative Gaucher Group (ICGG) Gaucher Registry.

Authors:  Pramod K Mistry; Julie L Batista; Hans C Andersson; Manisha Balwani; Thomas Andrew Burrow; Joel Charrow; Paige Kaplan; Aneal Khan; Priya S Kishnani; Edwin H Kolodny; Barry Rosenbloom; C Ronald Scott; Neal Weinreb
Journal:  Am J Hematol       Date:  2017-07-07       Impact factor: 10.047

6.  A Quantitative Systems Pharmacology Model of Gaucher Disease Type 1 Provides Mechanistic Insight Into the Response to Substrate Reduction Therapy With Eliglustat.

Authors:  Ruth Abrams; Chanchala D Kaddi; Mengdi Tao; Randolph J Leiser; Giulia Simoni; Federico Reali; John Tolsma; Paul Jasper; Zachary van Rijn; Jing Li; Bradley Niesner; Jeffrey S Barrett; Luca Marchetti; M Judith Peterschmitt; Karim Azer; Susana Neves-Zaph
Journal:  CPT Pharmacometrics Syst Pharmacol       Date:  2020-06-19

7.  Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1.

Authors:  Anca Zimmermann; Radu A Popp; Heidi Rossmann; Simona Bucerzan; Ioana Nascu; Daniel Leucuta; Matthias M Weber; Paula Grigorescu-Sido
Journal:  Ther Clin Risk Manag       Date:  2018-10-24       Impact factor: 2.423

8.  Impaired autophagic and mitochondrial functions are partially restored by ERT in Gaucher and Fabry diseases.

Authors:  Margarita M Ivanova; Erk Changsila; Chidima Iaonou; Ozlem Goker-Alpan
Journal:  PLoS One       Date:  2019-01-11       Impact factor: 3.240

Review 9.  Gaucher Disease in Bone: From Pathophysiology to Practice.

Authors:  Derralynn Hughes; Peter Mikosch; Nadia Belmatoug; Francesca Carubbi; TimothyM Cox; Ozlem Goker-Alpan; Andreas Kindmark; PramodK Mistry; Ludger Poll; Neal Weinreb; Patrick Deegan
Journal:  J Bone Miner Res       Date:  2019-06-24       Impact factor: 6.741

10.  Time of Initiating Enzyme Replacement Therapy Affects Immune Abnormalities and Disease Severity in Patients with Gaucher Disease.

Authors:  Renuka Pudi Limgala; Chidima Ioanou; Matthew Plassmeyer; Mark Ryherd; Lina Kozhaya; Lauren Austin; Cem Abidoglu; Derya Unutmaz; Oral Alpan; Ozlem Goker-Alpan
Journal:  PLoS One       Date:  2016-12-12       Impact factor: 3.240

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