Literature DB >> 24492980

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.

Saskia M Rombach1, Bouwien E Smid, Gabor E Linthorst, Marcel G W Dijkgraaf, Carla E M Hollak.   

Abstract

OBJECTIVE: Current available evidence on long-term effectiveness of enzyme replacement therapy (ERT) for Fabry disease is limited. More insight is needed whether ERT effectiveness differs in patients with and without baseline end-organ damage.
DESIGN: Through a systematic review, untreated and ERT treated males and females with Fabry disease were compared for main clinical outcomes: renal function, left ventricular mass (LVmass), cerebral white matter lesions (WMLs) and end-organ complications. Through a meta-analysis ERT effectiveness was estimated in different disease stages. DATA EXTRACTION: Two reviewers assessed quality of the included studies according to guidelines for prognosis research. Data were synthesized using a random effects meta-analysis.
RESULTS: Thirty-one studies were systematically reviewed while six studies were included in the meta-analysis. In patients with a GFR > 60 ml/min/1.73 m(2), decline of renal function was similar for treated and untreated patients. Only ERT treated males with a GFR < 60 ml/min/1.73 m(2) had a slower rate of decline in renal function, possibly attributable to anti-proteinuric therapy. Regardless of left ventricular hypertrophy (LVH) at baseline, LVmass remained stable or increased in males despite ERT, however at a slower rate compared to untreated male patients. In ERT treated females with LVH LVmass decreased, and remained stable in females without LVH. WMLs can not be prevented by ERT. Stroke, cardiac and end-stage renal complications develop, though the incidence of new complications seems to be reduced during ERT.
CONCLUSION: ERT is effective in reducing LVH, but has a limited effect on renal function. Improved treatment options are needed for Fabry disease.

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Year:  2014        PMID: 24492980     DOI: 10.1007/s10545-014-9677-8

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  100 in total

1.  Onset and progression of the Anderson-Fabry disease related cardiomyopathy.

Authors:  Christoph Kampmann; Ales Linhart; Frank Baehner; Tomas Palecek; Christiane M Wiethoff; Elke Miebach; Catharina Whybra; Andreas Gal; Jan Bultas; Michael Beck
Journal:  Int J Cardiol       Date:  2008-06-24       Impact factor: 4.164

2.  Enzyme replacement therapy improves cardiac features and severity of Fabry disease.

Authors:  Manish Motwani; Sanjay Banypersad; Peter Woolfson; Stephen Waldek
Journal:  Mol Genet Metab       Date:  2012-05-29       Impact factor: 4.797

3.  Safety of agalsidase alfa in patients with Fabry disease under 7 years.

Authors:  U Ramaswami; R Parini; C Kampmann; M Beck
Journal:  Acta Paediatr       Date:  2011-01-12       Impact factor: 2.299

4.  Fabry disease: overall effects of agalsidase alfa treatment.

Authors:  M Beck; R Ricci; U Widmer; F Dehout; A García de Lorenzo; C Kampmann; A Linhart; G Sunder-Plassmann; G Houge; U Ramaswami; A Gal; A Mehta
Journal:  Eur J Clin Invest       Date:  2004-12       Impact factor: 4.686

5.  Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data.

Authors:  A Mehta; M Beck; P Elliott; R Giugliani; A Linhart; G Sunder-Plassmann; R Schiffmann; F Barbey; M Ries; J T R Clarke
Journal:  Lancet       Date:  2009-12-12       Impact factor: 79.321

6.  Effect of agalsidase alfa replacement therapy on Fabry disease-related hypertrophic cardiomyopathy: a 12- to 36-month, retrospective, blinded echocardiographic pooled analysis.

Authors:  Christoph Kampmann; Ales Linhart; Richard B Devereux; Raphael Schiffmann
Journal:  Clin Ther       Date:  2009-09       Impact factor: 3.393

7.  Antiproteinuric therapy and fabry nephropathy: sustained reduction of proteinuria in patients receiving enzyme replacement therapy with agalsidase-beta.

Authors:  Hindia Tahir; Leslie L Jackson; David G Warnock
Journal:  J Am Soc Nephrol       Date:  2007-07-26       Impact factor: 10.121

8.  Enzyme replacement therapy in heterozygous females with Fabry disease: results of a phase IIIB study.

Authors:  F Baehner; C Kampmann; C Whybra; E Miebach; C M Wiethoff; M Beck
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

9.  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

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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  47 in total

1.  A prospective 10-year study of individualized, intensified enzyme replacement therapy in advanced Fabry disease.

Authors:  Raphael Schiffmann; Caren Swift; Xuan Wang; Derek Blankenship; Markus Ries
Journal:  J Inherit Metab Dis       Date:  2015-04-22       Impact factor: 4.982

Review 2.  Lysosomal storage disease overview.

Authors:  Angela Sun
Journal:  Ann Transl Med       Date:  2018-12

Review 3.  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

4.  The Changing Landscape of Fabry Disease.

Authors:  Einar Svarstad; Hans Peter Marti
Journal:  Clin J Am Soc Nephrol       Date:  2020-03-04       Impact factor: 8.237

5.  Innate and Adaptive Immune Response in Fabry Disease.

Authors:  Wladimir Mauhin; Olivier Lidove; Elisa Masat; Federico Mingozzi; Kuberaka Mariampillai; Jean-Marc Ziza; Olivier Benveniste
Journal:  JIMD Rep       Date:  2015-02-18

Review 6.  Restrictive cardiomyopathy in a patient with systemic sclerosis and Fabry disease: a case-based review.

Authors:  Álvaro Arbeláez-Cortés; Diana C Quintero-González; Yesid Cuesta-Astroz; Juan S Villadiego; Herman González-Buriticá; Jorge M Rueda
Journal:  Rheumatol Int       Date:  2019-10-10       Impact factor: 2.631

Review 7.  Precision medicine for cardiovascular disease : Learning lessons from cardiomyopathies.

Authors:  F Sedaghat-Hamedani; H A Katus; B Meder
Journal:  Herz       Date:  2018-03       Impact factor: 1.443

Review 8.  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

9.  Long-term enzyme replacement therapy for Fabry disease: efficacy and unmet needs in cardiac and renal outcomes.

Authors:  Ja Hye Kim; Beom Hee Lee; Ja Hyang Cho; Eungu Kang; Jin-Ho Choi; Gu-Hwan Kim; Han-Wook Yoo
Journal:  J Hum Genet       Date:  2016-06-23       Impact factor: 3.172

Review 10.  Fabry Disease: Recognition, Diagnosis, and Treatment of Neurological Features.

Authors:  Michela Ranieri; Gloria Bedini; Eugenio Agostino Parati; Anna Bersano
Journal:  Curr Treat Options Neurol       Date:  2016-07       Impact factor: 3.598

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