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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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 |
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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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