Long-term Outcomes of Kidney Transplantation in Fabry Disease. Issue 11 (November 2018)
- Record Type:
- Journal Article
- Title:
- Long-term Outcomes of Kidney Transplantation in Fabry Disease. Issue 11 (November 2018)
- Main Title:
- Long-term Outcomes of Kidney Transplantation in Fabry Disease
- Authors:
- Ersözlü, Sara
Desnick, Robert J.
Huynh-Do, Uyen
Canaan-Kühl, Sima
Barbey, Frédéric
Genitsch, Vera
Mueller, Thomas F.
Cheetham, Marcus
Flammer, Andreas J.
Schaub, Stefan
Nowak, Albina - Abstract:
- Abstract : Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by mutations in the α-galactosidase A gene that obliterate or markedly reduce α-galactosidase A activity. This results in the systemic accumulation of its glycosphingolipid substrates in body fluids and organs, including the kidney. Fabry nephropathy can lead to end-stage renal disease requiring kidney transplantation. Little is known about its long-term outcomes and the overall patient survival after kidney transplantation. Methods: Here, we report 17 Fabry patients (15 male and 2 female subjects) who received kidney transplants and their long-term treatment and follow-up at 4 specialized Fabry centers. Results: The posttransplant follow-up ranged to 25 years, with a median of 11.5 (range, 0.8-25.5] years. Graft survival was similar, and death-censored graft survival was superior to matched controls. Fabry patients died with functioning kidneys, mostly from cardiac causes. In 2 male subjects 14 and 23 years posttransplant, the grafts had a few typical FD lamellar inclusions, presumably originating from invading host macrophages and vascular endothelial cells. Conclusions: We conclude that kidney transplantation has an excellent long-term outcome in FD. Abstract : This retrospective cohort study suggests that patients with chronic kidney disease due to Fabry disease who receive a kidney transplant and enzyme replacement therapy show long-term patient and graft survival that are atAbstract : Background: Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by mutations in the α-galactosidase A gene that obliterate or markedly reduce α-galactosidase A activity. This results in the systemic accumulation of its glycosphingolipid substrates in body fluids and organs, including the kidney. Fabry nephropathy can lead to end-stage renal disease requiring kidney transplantation. Little is known about its long-term outcomes and the overall patient survival after kidney transplantation. Methods: Here, we report 17 Fabry patients (15 male and 2 female subjects) who received kidney transplants and their long-term treatment and follow-up at 4 specialized Fabry centers. Results: The posttransplant follow-up ranged to 25 years, with a median of 11.5 (range, 0.8-25.5] years. Graft survival was similar, and death-censored graft survival was superior to matched controls. Fabry patients died with functioning kidneys, mostly from cardiac causes. In 2 male subjects 14 and 23 years posttransplant, the grafts had a few typical FD lamellar inclusions, presumably originating from invading host macrophages and vascular endothelial cells. Conclusions: We conclude that kidney transplantation has an excellent long-term outcome in FD. Abstract : This retrospective cohort study suggests that patients with chronic kidney disease due to Fabry disease who receive a kidney transplant and enzyme replacement therapy show long-term patient and graft survival that are at least comparable to matched controls. … (more)
- Is Part Of:
- Transplantation. Volume 102:Issue 11(2018)
- Journal:
- Transplantation
- Issue:
- Volume 102:Issue 11(2018)
- Issue Display:
- Volume 102, Issue 11 (2018)
- Year:
- 2018
- Volume:
- 102
- Issue:
- 11
- Issue Sort Value:
- 2018-0102-0011-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-11
- Subjects:
- Transplantation of organs, tissues, etc -- Periodicals
Transplantation immunology -- Periodicals
617.95 - Journal URLs:
- http://journals.lww.com/pages/default.aspx ↗
- DOI:
- 10.1097/TP.0000000000002252 ↗
- Languages:
- English
- ISSNs:
- 0041-1337
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9024.990000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 11214.xml