Literature DB >> 20962662

Effects of enzyme replacement therapy in Fabry disease--a comprehensive review of the medical literature.

Olivier Lidove1, Michael L West, Guillem Pintos-Morell, Ricardo Reisin, Kathy Nicholls, Luis E Figuera, Rossella Parini, Luiz R Carvalho, Christoph Kampmann, Gregory M Pastores, Atul Mehta.   

Abstract

Enzyme replacement therapy with α-galactosidase A has been used to treat Fabry disease since 2001. This article reviews the published evidence for clinical efficacy of the two available enzyme preparations. We focused on heart, kidney, and nervous system manifestations, which impact both quality of life and overall prognosis. A literature search was undertaken to identify prospective open or randomized controlled trials of enzyme replacement therapy in patients with Fabry disease published since 2001. To date, no definitive conclusion can be drawn from studies that have directly compared therapeutic responses between the two commercially available enzyme preparations. Significant clinical benefits of enzyme replacement therapy have been demonstrated, mainly in patients at an early phase of the disease, with beneficial effects on heart, kidneys, pain, and quality of life in treated patients. Incidence of antibodies against agalsidase alfa and agalsidase beta observed during major clinical studies suggests a greater antigenic response to agalsidase beta. Further studies are required to confirm the long-term clinical benefits of enzyme replacement therapy. More studies with female patients are needed as are investigations of early initiation of enzyme replacement therapy to determine the optimal time to start treatment to prevent irreversible organ damage. The value of adjunctive and supportive therapies should also be rigorously analyzed.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20962662     DOI: 10.1097/GIM.0b013e3181f13b75

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  38 in total

1.  Unravelling the mechanism of action of enzyme replacement therapy in Fabry disease.

Authors:  Younhee Ko; CheolHo Lee; Myeong Hee Moon; Geu-Ru Hong; Chong-Kun Cheon; Jin-Sung Lee
Journal:  J Hum Genet       Date:  2015-10-22       Impact factor: 3.172

2.  Clinical utility gene card for: Fabry disease.

Authors:  Andreas Gal; Michael Beck; Bryan Winchester
Journal:  Eur J Hum Genet       Date:  2011-09-21       Impact factor: 4.246

3.  Effects of switching from agalsidase Beta to agalsidase alfa in 10 patients with anderson-fabry disease.

Authors:  A Pisani; L Spinelli; B Visciano; I Capuano; M Sabbatini; E Riccio; G Messalli; M Imbriaco
Journal:  JIMD Rep       Date:  2012-10-21

4.  Considering Fabry, but Diagnosing MPS I: Difficulties in the Diagnostic Process.

Authors:  E J Langereis; I E T van den Berg; D J J Halley; B J H M Poorthuis; F M Vaz; J H J Wokke; G E Linthorst
Journal:  JIMD Rep       Date:  2012-10-30

Review 5.  Effects of Enzyme Replacement Therapy and Antidrug Antibodies in Patients with Fabry Disease.

Authors:  Malte Lenders; Eva Brand
Journal:  J Am Soc Nephrol       Date:  2018-08-09       Impact factor: 10.121

Review 6.  Natural course of Fabry disease and the effectiveness of enzyme replacement therapy: a systematic review and meta-analysis: effectiveness of ERT in different disease stages.

Authors:  Saskia M Rombach; Bouwien E Smid; Gabor E Linthorst; Marcel G W Dijkgraaf; Carla E M Hollak
Journal:  J Inherit Metab Dis       Date:  2014-02-04       Impact factor: 4.982

Review 7.  Stroke and Fabry disease.

Authors:  Miguel Viana-Baptista
Journal:  J Neurol       Date:  2011-10-27       Impact factor: 4.849

8.  Synergy between the pharmacological chaperone 1-deoxygalactonojirimycin and the human recombinant alpha-galactosidase A in cultured fibroblasts from patients with Fabry disease.

Authors:  Caterina Porto; Antonio Pisani; Margherita Rosa; Emma Acampora; Valeria Avolio; Maria Rosaria Tuzzi; Bianca Visciano; Cristina Gagliardo; Serena Materazzi; Giancarlo la Marca; Generoso Andria; Giancarlo Parenti
Journal:  J Inherit Metab Dis       Date:  2011-12-21       Impact factor: 4.982

9.  Long-term, high-level hepatic secretion of acid α-glucosidase for Pompe disease achieved in non-human primates using helper-dependent adenovirus.

Authors:  D P W Rastall; S S Seregin; Y A Aldhamen; L M Kaiser; C Mullins; A Liou; F Ing; C Pereria-Hicks; S Godbehere-Roosa; D Palmer; P Ng; A Amalfitano
Journal:  Gene Ther       Date:  2016-07-01       Impact factor: 5.250

10.  Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy.

Authors:  Jessica R Golbus; Megan J Puckelwartz; Lisa Dellefave-Castillo; John P Fahrenbach; Viswateja Nelakuditi; Lorenzo L Pesce; Peter Pytel; Elizabeth M McNally
Journal:  Circ Cardiovasc Genet       Date:  2014-09-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.