Literature DB >> 16580615

Diagnosis and management of kidney involvement in Fabry disease.

David G Warnock1, Michael L West.   

Abstract

Interest in the diagnosis and treatment of Fabry disease has been greatly stimulated by the availability of Food and Drug Administration-approved, effective enzyme replacement therapy. This review will update the progress in this area since enzyme replacement therapy has become available. Fabry disease is often associated with proteinuric chronic kidney disease (CKD), and it appears that the treatment paradigms that have proven to be so effective in diabetes mellitus and other forms of proteinuric kidney disease are also effective in conjunction with enzyme replacement therapy for treating the kidney manifestations of Fabry disease. As such, Fabry disease represents an interesting example of progressive proteinuric kidney disease in which the usual blood pressure is lower than in other forms of CKD. This makes the use of effective antiproteinuric therapy challenging, especially considering the autonomic dysfunction that appears to be part of the disease. Comprehensive therapy for Fabry disease includes enzyme replacement therapy and all of the adjunctive therapies that are currently used to treat all forms of proteinuric CKD. It is anticipated that this approach will preserve kidney function and also benefit the cardiac and cerebrovascular systems in patients with Fabry disease.

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Year:  2006        PMID: 16580615     DOI: 10.1053/j.ackd.2006.01.013

Source DB:  PubMed          Journal:  Adv Chronic Kidney Dis        ISSN: 1548-5595            Impact factor:   3.620


  3 in total

1.  Successful management of enzyme replacement therapy in related fabry disease patients with severe adverse events by switching from agalsidase Beta (fabrazyme(®)) to agalsidase alfa (replagal (®)).

Authors:  Kazuya Tsuboi; Hiroshi Yamamoto; Fuji Somura; Hiromi Goto
Journal:  JIMD Rep       Date:  2014-04-10

Review 2.  "Treasure your exceptions": recent advances in molecular genetics of glomerular disease.

Authors:  Andrzej Ciechanowicz; Andrzej Brodkiewicz; Agnieszka Bińczak-Kuleta; Miłosz Parczewski; Stanłisaw Czekalski
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240

3.  Urine bikunin as a marker of renal impairment in Fabry's disease.

Authors:  Antonio Junior Lepedda; Laura Fancellu; Elisabetta Zinellu; Pierina De Muro; Gabriele Nieddu; Giovanni Andrea Deiana; Piera Canu; Daniela Concolino; Simona Sestito; Marilena Formato; Gianpietro Sechi
Journal:  Biomed Res Int       Date:  2013-06-12       Impact factor: 3.411

  3 in total

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