Literature DB >> 20464743

Enzyme replacement therapy for Anderson-Fabry disease.

Regina P El Dib1, Gregory M Pastores.   

Abstract

BACKGROUND: Anderson-Fabry disease is an X-linked defect of glycosphingolipid metabolism. Progressive renal insufficiency is a major source of morbidity, additional complications result from cardio- and cerebro-vascular involvement. Survival is reduced among affected males and symptomatic female carriers.
OBJECTIVES: To evaluate the effectiveness and safety of enzyme replacement therapy compared to other interventions, placebo or no interventions, for treating Anderson-Fabry disease. SEARCH STRATEGY: We searched 'Clinical Trials' on The Cochrane Library, MEDLINE, EMBASE, LILACS and the Cystic Fibrosis and Genetic Disorders Group's Inborn Errors of Metabolism Trials Register (date of the most recent search: 07 April 2010). SELECTION CRITERIA: Randomized controlled trials of agalsidase alfa or beta in participants diagnosed with Anderson-Fabry disease. DATA COLLECTION AND ANALYSIS: Two authors selected relevant trials, assessed methodological quality and extracted data. MAIN
RESULTS: Five studies comparing either agalsidase alfa or beta in 187 participants fulfilled the selection criteria.Both trials comparing agalsidase alfa to placebo reported on globotriaosylceramide concentration in plasma and tissue; aggregate results were non-significant. One study reported pain scores, there was a statistically significant improvement for participants receiving treatment at up to three months, mean difference -2.10 (95% confidence interval (CI) -3.79 to -0.41); at up to five months, mean difference -1.90 (95% CI -3.65 to -0.15); and at up to six months, mean difference -2.00 (95% CI -3.66 to -0.34). There was a significant difference in pain-related quality of life at over five months and up to six months, mean difference -2.10 (95% CI -3.92 to -0.28) but not at other time-points. Neither study reported deaths.One of the three trials comparing agalsidase beta to placebo reported on globotriaosylceramide concentration in plasma and tissue and showed significant improvement: kidney, mean difference -1.70 (95% CI -2.09 to -1.31); heart, mean difference -0.90 (95% CI -1.18 to -0.62); and composite results (renal, cardiac, and cerebrovascular complications and death), mean difference -4.80 (95% CI -5.45 to -4.15). There was no significant difference between groups for death; no studies reported on pain. AUTHORS'
CONCLUSIONS: Five small, poor quality randomised controlled trials provide no robust evidence for use of either agalsidase alfa and beta to treat Anderson-Fabry disease.

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Year:  2010        PMID: 20464743     DOI: 10.1002/14651858.CD006663.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  7 in total

1.  Effect of reduced agalsidase Beta dosage in fabry patients: the Australian experience.

Authors:  Joanna Ghali; Kathy Nicholls; Charles Denaro; David Sillence; Ian Chapman; Jack Goldblatt; Mark Thomas; Janice Fletcher
Journal:  JIMD Rep       Date:  2011-09-15

2.  Enzyme enhancers for the treatment of Fabry and Pompe disease.

Authors:  Jan Lukas; Anne-Marie Pockrandt; Susanne Seemann; Muhammad Sharif; Franziska Runge; Susann Pohlers; Chaonan Zheng; Anne Gläser; Matthias Beller; Arndt Rolfs; Anne-Katrin Giese
Journal:  Mol Ther       Date:  2014-11-20       Impact factor: 11.454

Review 3.  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 4.  Enzyme replacement therapy for Anderson-Fabry disease.

Authors:  Regina El Dib; Huda Gomaa; Raíssa Pierri Carvalho; Samira E Camargo; Rodrigo Bazan; Pasqual Barretti; Fellype C Barreto
Journal:  Cochrane Database Syst Rev       Date:  2016-07-25

Review 5.  [Fabry disease : diagnosis and treatment].

Authors:  N Üçeyler; C Sommer
Journal:  Schmerz       Date:  2012-09       Impact factor: 1.107

6.  Enzyme replacement therapy for Fabry disease: A systematic review and meta-analysis.

Authors:  Taciane Alegra; Filippo Vairo; Monica V de Souza; Bárbara C Krug; Ida V D Schwartz
Journal:  Genet Mol Biol       Date:  2012-12-18       Impact factor: 1.771

7.  A distinct urinary biomarker pattern characteristic of female Fabry patients that mirrors response to enzyme replacement therapy.

Authors:  Andreas D Kistler; Justyna Siwy; Frank Breunig; Praveen Jeevaratnam; Alexander Scherl; William Mullen; David G Warnock; Christoph Wanner; Derralynn A Hughes; Harald Mischak; Rudolf P Wüthrich; Andreas L Serra
Journal:  PLoS One       Date:  2011-06-15       Impact factor: 3.240

  7 in total

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