Kidney Transplant in Fabry Disease: A Revision of the Literature

Bibliographic Details
Title: Kidney Transplant in Fabry Disease: A Revision of the Literature
Authors: Irene Capelli, Valeria Aiello, Lorenzo Gasperoni, Giorgia Comai, Valeria Corradetti, Matteo Ravaioli, Elena Biagini, Claudio Graziano, Gaetano La Manna
Source: Medicina, Vol 56, Iss 6, p 284 (2020)
Publisher Information: MDPI AG, 2020.
Publication Year: 2020
Collection: LCC:Medicine (General)
Subject Terms: enzyme replacement therapy, Fabry disease, Fabry nephropathy, kidney transplant, Medicine (General), R5-920
More Details: Fabry disease is classified as a rare X-linked disease caused by a complete or partial defect of enzyme alpha-galactosidase, due to GLA gene mutations. This disorder leads to intracellular globotriaosylceramide (Gb3) deposition associated with increased Gb3 plasma levels. Most of the symptoms of the disease, involving kidneys, heart and nervous system, result from this progressive Gb3 deposition. The incidence is estimated in 1/50,000 to 1/117,000 in males. Fabry nephropathy begins with microalbuminuria and/or proteinuria, which, in the classic form, appear from childhood. Thus, a progressive decline of renal function can start at a young age, and evolve to kidney failure, requiring dialysis or renal transplantation. Enzyme replacement therapy (ERT), available since 2001 for Fabry disease, has been increasingly introduced into the clinical practice, with overall positive short-term and long-term effects in terms of ventricular hypertrophy and renal function. Kidney transplantation represents a relevant therapeutic option for Fabry nephropathy management, for patients reaching end-stage renal disease, but little is known about long-term outcomes, overall patient survival or the possible role of ERT after transplant. The purpose of this review is to analyze the literature on every aspect related to kidney transplantation in patients with Fabry nephropathy: from the analysis of transplant outcomes, to the likelihood of disease recurrence, up to the effects of ERT and its possible interference with immunosuppression.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1648-9144
1010-660X
Relation: https://www.mdpi.com/1648-9144/56/6/284; https://doaj.org/toc/1010-660X; https://doaj.org/toc/1648-9144
DOI: 10.3390/medicina56060284
Access URL: https://doaj.org/article/1ede27bf3a594ad4bd7a680909f0495c
Accession Number: edsdoj.1ede27bf3a594ad4bd7a680909f0495c
Database: Directory of Open Access Journals
More Details
ISSN:16489144
1010660X
DOI:10.3390/medicina56060284
Published in:Medicina
Language:English