Literature DB >> 25987174

The attenuated/late onset lysosomal storage disorders: Therapeutic goals and indications for enzyme replacement treatment in Gaucher and Fabry disease.

Carla E M Hollak1, Neal J Weinreb2.   

Abstract

Enzyme replacement therapies have been developed and authorized for commercial use for six different lysosomal storage disorders. For Gaucher disease, Fabry disease and mucopolysaccharidosis type 1, disease-specific treatments have been available for more than a decade. Although long term follow-up data are still sparse, therapeutic goals for patients with Gaucher disease and Fabry disease have been formulated and published for both adults and children. Without adaptation or modification, these goals are often applied in clinical research and in routine patient care across the entire phenotypic spectrum of disease, although in practice, patients commonly manifest high variability in clinical presentation and course of the illness. In this context, establishing goals for the follow-up and treatment of late onset/attenuated phenotypes is particularly challenging. In this chapter, we review current therapeutic goals for Gaucher disease and Fabry disease and discuss approaches for those with attenuated disease manifestations.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Fabry disease; Gaucher disease; attenuated phenotypes; enzyme replacement therapy; late onset; therapeutic goals

Mesh:

Year:  2014        PMID: 25987174     DOI: 10.1016/j.beem.2014.08.006

Source DB:  PubMed          Journal:  Best Pract Res Clin Endocrinol Metab        ISSN: 1521-690X            Impact factor:   4.690


  7 in total

Review 1.  Lysosomal Leukodystrophies Lysosomal Storage Diseases Associated With White Matter Abnormalities.

Authors:  Gustavo H B Maegawa
Journal:  J Child Neurol       Date:  2019-02-13       Impact factor: 1.987

2.  Selective screening for lysosomal storage disorders in a large cohort of minorities of African descent shows high prevalence rates and novel variants.

Authors:  Renuka Pudi Limgala; Vyacheslav Furtak; Margarita M Ivanova; Erk Changsila; Floyd Wilks; Marie N Fidelia-Lambert; Ozlem Goker-Alpan; Marjorie C Gondré-Lewis
Journal:  JIMD Rep       Date:  2021-01-27

Review 3.  The Large Phenotypic Spectrum of Fabry Disease Requires Graduated Diagnosis and Personalized Therapy: A Meta-Analysis Can Help to Differentiate Missense Mutations.

Authors:  Valentina Citro; Marco Cammisa; Ludovica Liguori; Chiara Cimmaruta; Jan Lukas; Maria Vittoria Cubellis; Giuseppina Andreotti
Journal:  Int J Mol Sci       Date:  2016-12-01       Impact factor: 5.923

Review 4.  From Lysosomal Storage Diseases to NKT Cell Activation and Back.

Authors:  Cátia S Pereira; Helena Ribeiro; M Fatima Macedo
Journal:  Int J Mol Sci       Date:  2017-02-25       Impact factor: 5.923

5.  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

6.  The International Collaborative Gaucher Group GRAF (Gaucher Risk Assessment for Fracture) score: a composite risk score for assessing adult fracture risk in imiglucerase-treated Gaucher disease type 1 patients.

Authors:  Patrick Deegan; Aneal Khan; José Simon Camelo; Julie L Batista; Neal Weinreb
Journal:  Orphanet J Rare Dis       Date:  2021-02-18       Impact factor: 4.123

7.  Correction of pathology in mice displaying Gaucher disease type 1 by a clinically-applicable lentiviral vector.

Authors:  Maria Dahl; Emma M K Smith; Sarah Warsi; Michael Rothe; Maria J Ferraz; Johannes M F G Aerts; Azadeh Golipour; Claudia Harper; Richard Pfeifer; Daniella Pizzurro; Axel Schambach; Chris Mason; Stefan Karlsson
Journal:  Mol Ther Methods Clin Dev       Date:  2020-12-03       Impact factor: 6.698

  7 in total

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