Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis

Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder with progressive systemic deposition of globotriaosylceramide, leading to life-threatening cardiac, central nervous system, and kidney disease. Current therapy involves symptomatic medical management, enzyme replacement the...

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Main Authors: Maria L. Gonzalez Suarez, Charat Thongprayoon, Panupong Hansrivijit, Juan Medaura, Pradeep Vaitla, Michael A. Mao, Tarun Bathini, Boonphiphop Boonpheng, Swetha R. Kanduri, Karthik Kovvuru, Arpita Basu, Wisit Cheungpasitporn
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Diseases
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Online Access:https://www.mdpi.com/2079-9721/9/1/2
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spelling doaj-0acf22b4987d464bafba19734d31b62d2020-12-24T00:02:25ZengMDPI AGDiseases2079-97212021-12-0192210.3390/diseases9010002Outcomes of Kidney Transplantation in Fabry Disease: A Meta-AnalysisMaria L. Gonzalez Suarez0Charat Thongprayoon1Panupong Hansrivijit2Juan Medaura3Pradeep Vaitla4Michael A. Mao5Tarun Bathini6Boonphiphop Boonpheng7Swetha R. Kanduri8Karthik Kovvuru9Arpita Basu10Wisit Cheungpasitporn11Division of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USADivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USADepartment of Internal Medicine, UPMC Pinnacle, Harrisburg, PA 17105, USADivision of Nephrology, Department of Internal Medicine, University of Mississippi Medical Center, Jackson, MS 39216, USADivision of Nephrology, Department of Internal Medicine, University of Mississippi Medical Center, Jackson, MS 39216, USADivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Jacksonville, FL 32224, USADepartment of Internal Medicine, University of Arizona, Tucson, AZ 85721, USADepartment of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USADivision of Nephrology, Ochsner Medical Center, New Orleans, LA 70121, USADivision of Nephrology, Ochsner Medical Center, New Orleans, LA 70121, USAEmory Transplant Center and Department of Medicine, Renal Division, Emory University School of Medicine, Atlanta, GA 30322, USADivision of Nephrology and Hypertension, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USABackground: Fabry disease (FD) is a rare X-linked lysosomal storage disorder with progressive systemic deposition of globotriaosylceramide, leading to life-threatening cardiac, central nervous system, and kidney disease. Current therapy involves symptomatic medical management, enzyme replacement therapy (ERT), dialysis, kidney transplantation, and, more recently, gene therapy. The aim of this systematic review was to assess outcomes of kidney transplantation among patients with FD. Methods: A comprehensive literature review was conducted utilizing MEDLINE, EMBASE, and Cochrane Database, from inception through to 28 February 2020, to identify studies that evaluate outcomes of kidney transplantation including patient and allograft survival among kidney transplant patients with FD. Effect estimates from each study were extracted and combined using the random-effects generic inverse variance method of DerSimonian and Laird. Results: In total, 11 studies, including 424 kidney transplant recipients with FD, were enrolled. The post-transplant median follow-up time ranged from 3 to 11.5 years. Overall, the pooled estimated rates of all-cause graft failure, graft failure before death, and allograft rejection were 32.5% (95%CI: 23.9%–42.5%), 14.5% (95%CI: 8.4%–23.7%), and 20.2% (95%CI: 15.4%–25.9%), respectively. In the sensitivity analysis, limited only to the recent studies (year 2001 or newer when ERT became available), the pooled estimated rates of all-cause graft failure, graft failure before death, and allograft rejection were 28.1% (95%CI: 20.5%–37.3%), 11.7% (95%CI: 8.4%–16.0%), and 20.2% (95%CI: 15.5%–26.0%), respectively. The pooled estimated rate of biopsy proven FD recurrence was 11.1% (95%CI: 3.6%–29.4%), respectively. There are no significant differences in the risks of all-cause graft failure (<i>p</i> = 0.10) or mortality (0.48) among recipients with vs. without FD. Conclusions: Despite possible FD recurrence after transplantation of 11.1%, allograft and patient survival are comparable among kidney transplant recipients with vs. without FD.https://www.mdpi.com/2079-9721/9/1/2Fabry diseasekidney transplantkidney transplantationmeta-analysissystematic review
collection DOAJ
language English
format Article
sources DOAJ
author Maria L. Gonzalez Suarez
Charat Thongprayoon
Panupong Hansrivijit
Juan Medaura
Pradeep Vaitla
Michael A. Mao
Tarun Bathini
Boonphiphop Boonpheng
Swetha R. Kanduri
Karthik Kovvuru
Arpita Basu
Wisit Cheungpasitporn
spellingShingle Maria L. Gonzalez Suarez
Charat Thongprayoon
Panupong Hansrivijit
Juan Medaura
Pradeep Vaitla
Michael A. Mao
Tarun Bathini
Boonphiphop Boonpheng
Swetha R. Kanduri
Karthik Kovvuru
Arpita Basu
Wisit Cheungpasitporn
Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
Diseases
Fabry disease
kidney transplant
kidney transplantation
meta-analysis
systematic review
author_facet Maria L. Gonzalez Suarez
Charat Thongprayoon
Panupong Hansrivijit
Juan Medaura
Pradeep Vaitla
Michael A. Mao
Tarun Bathini
Boonphiphop Boonpheng
Swetha R. Kanduri
Karthik Kovvuru
Arpita Basu
Wisit Cheungpasitporn
author_sort Maria L. Gonzalez Suarez
title Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
title_short Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
title_full Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
title_fullStr Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
title_full_unstemmed Outcomes of Kidney Transplantation in Fabry Disease: A Meta-Analysis
title_sort outcomes of kidney transplantation in fabry disease: a meta-analysis
publisher MDPI AG
series Diseases
issn 2079-9721
publishDate 2021-12-01
description Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder with progressive systemic deposition of globotriaosylceramide, leading to life-threatening cardiac, central nervous system, and kidney disease. Current therapy involves symptomatic medical management, enzyme replacement therapy (ERT), dialysis, kidney transplantation, and, more recently, gene therapy. The aim of this systematic review was to assess outcomes of kidney transplantation among patients with FD. Methods: A comprehensive literature review was conducted utilizing MEDLINE, EMBASE, and Cochrane Database, from inception through to 28 February 2020, to identify studies that evaluate outcomes of kidney transplantation including patient and allograft survival among kidney transplant patients with FD. Effect estimates from each study were extracted and combined using the random-effects generic inverse variance method of DerSimonian and Laird. Results: In total, 11 studies, including 424 kidney transplant recipients with FD, were enrolled. The post-transplant median follow-up time ranged from 3 to 11.5 years. Overall, the pooled estimated rates of all-cause graft failure, graft failure before death, and allograft rejection were 32.5% (95%CI: 23.9%–42.5%), 14.5% (95%CI: 8.4%–23.7%), and 20.2% (95%CI: 15.4%–25.9%), respectively. In the sensitivity analysis, limited only to the recent studies (year 2001 or newer when ERT became available), the pooled estimated rates of all-cause graft failure, graft failure before death, and allograft rejection were 28.1% (95%CI: 20.5%–37.3%), 11.7% (95%CI: 8.4%–16.0%), and 20.2% (95%CI: 15.5%–26.0%), respectively. The pooled estimated rate of biopsy proven FD recurrence was 11.1% (95%CI: 3.6%–29.4%), respectively. There are no significant differences in the risks of all-cause graft failure (<i>p</i> = 0.10) or mortality (0.48) among recipients with vs. without FD. Conclusions: Despite possible FD recurrence after transplantation of 11.1%, allograft and patient survival are comparable among kidney transplant recipients with vs. without FD.
topic Fabry disease
kidney transplant
kidney transplantation
meta-analysis
systematic review
url https://www.mdpi.com/2079-9721/9/1/2
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