Literature DB >> 24850233

Fabry disease: multidisciplinary evaluation after 10 years of treatment with agalsidase Beta.

Politei Juan1, Amartino Hernan, Schenone Andrea Beatriz, Cabrera Gustavo, Michref Antonio, Tanus Eduardo, Dominguez Raul, Larralde Margarita, Blanco Mariana, Gaggioli Daniela, Szlago Marina.   

Abstract

UNLABELLED: Fabry disease is an X linked disorder of metabolism due to deficient α-galactosidase A activity. Enzyme replacement therapy (ERT) with agalsidase Beta was approved by EMA in 2001 and FDA in 2003. PATIENTS AND METHODS: Six patients were enrolled. Baseline data was measured for renal, cardiac, and cerebrovascular functioning. We compared baseline quality of life scales with the current results. These parameters were assessed during the 10 years of follow-up period.
RESULTS: Before ERT four patients showed normal eGFR, one stage 2 of CKD, and one hyperfiltration stage. All presented microalbuminuria and just two cases showed proteinuria. After 10 years of ERT, no patient showed decrease in renal functioning. One patient decreased from proteinuria to microalbuminuria range. Before treatment one case showed left ventricular (LV) hypertrophy and LV Mass Index was abnormal in two female patients. After 10 years echocardiographic values did not present progression to LVH and one female showed regression to normal values of LV posterior wall and interventricular septum. Brain MRI showed ischemic lesions in one female and vertebrobasilar dolichoectasia in one male. From baseline and during the follow-up period MRI did not progress to new ischemic lesions and there were no clinical signs of cerebrovascular damage. After 10 years quality of life showed improvement in all domains measured.
CONCLUSION: Early treatment of agalsidase Beta is related to a better outcome regarding stability and regression of signs and symptoms in Fabry disease. Our results in patients with mild organ involvement showed good outcomes and support an early and continuous ERT.

Entities:  

Year:  2014        PMID: 24850233      PMCID: PMC4221298          DOI: 10.1007/8904_2014_310

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  25 in total

1.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

2.  Enzyme replacement therapy in two Japanese siblings with Fabry disease, and its effectiveness on angiokeratoma and neuropathic pain.

Authors:  Mahoko Furujo; Toshihide Kubo; Masahisa Kobayashi; Toya Ohashi
Journal:  Mol Genet Metab       Date:  2013-07-14       Impact factor: 4.797

3.  Inner ear involvement in Anderson-Fabry disease: long-term follow-up during enzyme replacement therapy.

Authors:  B Sergi; G Conti; G Paludetti
Journal:  Acta Otorhinolaryngol Ital       Date:  2010-04       Impact factor: 2.124

4.  Enzyme replacement therapy in Fabry disease: a randomized controlled trial.

Authors:  R Schiffmann; J B Kopp; H A Austin; S Sabnis; D F Moore; T Weibel; J E Balow; R O Brady
Journal:  JAMA       Date:  2001-06-06       Impact factor: 56.272

5.  Long-term effects of enzyme replacement therapy on fabry cardiomyopathy: evidence for a better outcome with early treatment.

Authors:  Frank Weidemann; Markus Niemann; Frank Breunig; Sebastian Herrmann; Meinrad Beer; Stefan Störk; Wolfram Voelker; Georg Ertl; Christoph Wanner; Jörg Strotmann
Journal:  Circulation       Date:  2009-01-19       Impact factor: 29.690

6.  Agalsidase beta treatment is associated with improved quality of life in patients with Fabry disease: findings from the Fabry Registry.

Authors:  Torquil Watt; Alessandro P Burlina; Chiara Cazzorla; Dorothee Schönfeld; Maryam Banikazemi; Robert J Hopkin; Ana Maria Martins; Katherine Sims; Dana Beitner-Johnson; Fanny O'Brien; Ulla Feldt-Rasmussen
Journal:  Genet Med       Date:  2010-11       Impact factor: 8.822

7.  Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease.

Authors:  Natalie Jansen Street; Michael S Yi; Laurie A Bailey; Robert J Hopkin
Journal:  Genet Med       Date:  2006-06       Impact factor: 8.822

Review 8.  Fabry disease.

Authors:  Dominique P Germain
Journal:  Orphanet J Rare Dis       Date:  2010-11-22       Impact factor: 4.123

Review 9.  Fibrosis: a key feature of Fabry disease with potential therapeutic implications.

Authors:  Frank Weidemann; Maria D Sanchez-Niño; Juan Politei; João-Paulo Oliveira; Christoph Wanner; David G Warnock; Alberto Ortiz
Journal:  Orphanet J Rare Dis       Date:  2013-08-06       Impact factor: 4.123

10.  Long-term outcome of enzyme-replacement therapy in advanced Fabry disease: evidence for disease progression towards serious complications.

Authors:  F Weidemann; M Niemann; S Störk; F Breunig; M Beer; C Sommer; S Herrmann; G Ertl; C Wanner
Journal:  J Intern Med       Date:  2013-05-06       Impact factor: 8.989

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  6 in total

1.  Fabry's Disease: The Utility of a Multidisciplinary Screening Approach.

Authors:  Marco Angelo Monte; Massimiliano Veroux; Margherita Stefania Rodolico; Valentina Losi; Luigi Di Pino; Rita Bella; Giuseppe Lanza; Ines Paola Monte
Journal:  Life (Basel)       Date:  2022-04-22

Review 2.  Anderson-Fabry cardiomyopathy: prevalence, pathophysiology, diagnosis and treatment.

Authors:  Brendan N Putko; Kevin Wen; Richard B Thompson; John Mullen; Miriam Shanks; Haran Yogasundaram; Consolato Sergi; Gavin Y Oudit
Journal:  Heart Fail Rev       Date:  2015-03       Impact factor: 4.214

Review 3.  The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts.

Authors:  Dominique P Germain; Perry M Elliott; Bruno Falissard; Victor V Fomin; Max J Hilz; Ana Jovanovic; Ilkka Kantola; Aleš Linhart; Renzo Mignani; Mehdi Namdar; Albina Nowak; João-Paulo Oliveira; Maurizio Pieroni; Miguel Viana-Baptista; Christoph Wanner; Marco Spada
Journal:  Mol Genet Metab Rep       Date:  2019-02-06

4.  Agalsidase beta treatment slows estimated glomerular filtration rate loss in classic Fabry disease patients: results from an individual patient data meta-analysis.

Authors:  Alberto Ortiz; Steve Kanters; Alaa Hamed; Pronabesh DasMahapatra; Eugene Poggio; Manish Maski; Mario Aguiar; Elvira Ponce; Jeroen P Jansen; Dieter Ayers; Rachel Goldgrub; Robert J Desnick
Journal:  Clin Kidney J       Date:  2020-05-22

5.  Do clinical guidelines facilitate or impede drivers of treatment in Fabry disease?

Authors:  Derralynn A Hughes; Patrício Aguiar; Olivier Lidove; Kathleen Nicholls; Albina Nowak; Mark Thomas; Roser Torra; Bojan Vujkovac; Michael L West; Sandro Feriozzi
Journal:  Orphanet J Rare Dis       Date:  2022-02-08       Impact factor: 4.123

6.  Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis.

Authors:  Michael Beck; Derralynn Hughes; Christoph Kampmann; Sylvain Larroque; Atul Mehta; Guillem Pintos-Morell; Uma Ramaswami; Michael West; Anna Wijatyk; Roberto Giugliani
Journal:  Mol Genet Metab Rep       Date:  2015-03-05
  6 in total

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