Literature DB >> 18974635

Agalsidase alfa slows the decline in renal function in patients with Fabry disease.

Sandro Feriozzi1, Andreas Schwarting, Gere Sunder-Plassmann, Michael West, Markus Cybulla.   

Abstract

The aim of this study was to determine the effects of enzyme replacement therapy with agalsidase alpha on renal function in patients with Fabry nephropathy. Serum creatinine data were collected from 165 adult patients during 3 years of treatment. Serum creatinine increased in all men whereas it was stable in women, except in stage II renal disease (Kidney Disease Outcomes Quality Initiative). The estimated glomerular filtration rate (eGFR) declined in males with stage I and II (from 115.0 +/- 22.2 to 98.3 +/- 27.3 and from 76.5 +/- 8.1 to 66.3 +/-21.6 ml/min/1.73 m(2), respectively; both p < 0.01), whereas eGFR was stable in stage III. In females, eGFR was stable in stages I and III, and decreased in stage II (from 72.5 +/- 8.3 to 67.3 +/- 13.6 ml/min/1.73 m(2); p = 0.01). The 24-hour proteinuria was <1 g in all patients, and most patients (96%) were treated with angiotensin receptor blockers (ARBs) or angiotensin-converting enzyme (ACE) inhibitors. Agalsidase alpha in combination with ACE inhibitors/ARB may be effective in slowing the deterioration in renal function in Fabry nephropathy. Copyright (c) 2008 S. Karger AG, Basel.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18974635     DOI: 10.1159/000168482

Source DB:  PubMed          Journal:  Am J Nephrol        ISSN: 0250-8095            Impact factor:   3.754


  17 in total

Review 1.  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 2.  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

3.  The effectiveness of long-term agalsidase alfa therapy in the treatment of Fabry nephropathy.

Authors:  Sandro Feriozzi; Joan Torras; Markus Cybulla; Kathy Nicholls; Gere Sunder-Plassmann; Michael West
Journal:  Clin J Am Soc Nephrol       Date:  2012-01       Impact factor: 8.237

Review 4.  Renal complications of Fabry disease in children.

Authors:  Behzad Najafian; Michael Mauer; Robert J Hopkin; Einar Svarstad
Journal:  Pediatr Nephrol       Date:  2012-08-17       Impact factor: 3.714

Review 5.  Contemporary therapeutics and new drug developments for treatment of Fabry disease: a narrative review.

Authors:  Daniel Oder; Jonas Müntze; Peter Nordbeck
Journal:  Cardiovasc Diagn Ther       Date:  2021-04

Review 6.  [Effect of enzyme replacement therapy (ERT) on renal function of patients with Fabry's disease].

Authors:  Thomas Thomaidis; Manfred Relle; Joerg Reinke; Michael Beck; Andreas Schwarting
Journal:  Med Klin (Munich)       Date:  2009-09-23

7.  Early diagnosis of fabry disease in a patient with toe tip pain.

Authors:  Ki Bum Park; Kyung Ream Han; Jae Woo Lee; Seung Ho Kim; Do Wan Kim; Chan Kim; Jung Min Ko
Journal:  Korean J Pain       Date:  2010-08-26

Review 8.  Fabry disease-often seen, rarely diagnosed.

Authors:  Björn Hoffmann; Ertan Mayatepek
Journal:  Dtsch Arztebl Int       Date:  2009-06-26       Impact factor: 5.594

Review 9.  Fabry disease: recent advances in pathology, diagnosis, treatment and monitoring.

Authors:  Björn Hoffmann
Journal:  Orphanet J Rare Dis       Date:  2009-10-11       Impact factor: 4.123

Review 10.  Update on hypertrophic cardiomyopathy and a guide to the guidelines.

Authors:  Srijita Sen-Chowdhry; Daniel Jacoby; James C Moon; William J McKenna
Journal:  Nat Rev Cardiol       Date:  2016-09-29       Impact factor: 32.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.