Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type

Early hypertransaminasemia after kidney transplantation (KT) is frequent. It has been associated with the crosstalk produced between the liver and the kidney in ischemia-reperfusion situations. However, the influence of the donor type has not been evaluated. We present a retrospective study analyzin...

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Autores principales: Eulàlia Solà-Porta, Dolores Redondo-Pachón, Carlos Arias-Cabrales, Diego Navazo, Anna Buxeda, Carla Burballa, Marta Crespo, Montserrat García-Retortillo, Julio Pascual, María José Pérez-Sáez
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/7a4be361c9744bb2bc3df7fa2a9703d7
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spelling oai:doaj.org-article:7a4be361c9744bb2bc3df7fa2a9703d72021-11-11T17:46:57ZEarly Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type10.3390/jcm102151682077-0383https://doaj.org/article/7a4be361c9744bb2bc3df7fa2a9703d72021-11-01T00:00:00Zhttps://www.mdpi.com/2077-0383/10/21/5168https://doaj.org/toc/2077-0383Early hypertransaminasemia after kidney transplantation (KT) is frequent. It has been associated with the crosstalk produced between the liver and the kidney in ischemia-reperfusion situations. However, the influence of the donor type has not been evaluated. We present a retrospective study analyzing the increase in serum aspartate aminotransferase/alanine aminotransferase (AST/ALT) during the first three months post-KT in 151 recipients who received thymoglobulin as induction therapy, either from brain-death donors (DBD, <i>n</i> = 75), controlled circulatory death donors (cDCD, <i>n</i> = 33), or uncontrolled DCD (uDCD, <i>n</i> = 43). Eighty-five KT recipients from DBD who received basiliximab were included as controls. From KT recipients who received thymoglobulin, 33.6/43.4% presented with an increase in AST/ALT at 72 h post-KT, respectively. Regarding donor type, the percentage of recipients who experienced 72 h post-KT hypertransaminasemia was higher in uDCD group (65.1/83.7% vs. 20.3/26% in DBD and 20.7/27.6% in cDCD, <i>p</i> < 0.001). Within the control group, 9.4/12.9% of patients presented with AST/ALT elevation. One month after transplant, AST/ALT values returned to baseline in all groups. The multivariate analysis showed that uDCD recipients had 6- to 12-fold higher risk of developing early post-KT hypertransaminasemia. Early post-KT hypertransaminasemia is a frequent and transient event related to the kidney donor type, being more frequent in uDCD recipients.Eulàlia Solà-PortaDolores Redondo-PachónCarlos Arias-CabralesDiego NavazoAnna BuxedaCarla BurballaMarta CrespoMontserrat García-RetortilloJulio PascualMaría José Pérez-SáezMDPI AGarticledonor after circulatory deathearlyhypertransaminasemiakidney transplantationtransaminasesMedicineRENJournal of Clinical Medicine, Vol 10, Iss 5168, p 5168 (2021)
institution DOAJ
collection DOAJ
language EN
topic donor after circulatory death
early
hypertransaminasemia
kidney transplantation
transaminases
Medicine
R
spellingShingle donor after circulatory death
early
hypertransaminasemia
kidney transplantation
transaminases
Medicine
R
Eulàlia Solà-Porta
Dolores Redondo-Pachón
Carlos Arias-Cabrales
Diego Navazo
Anna Buxeda
Carla Burballa
Marta Crespo
Montserrat García-Retortillo
Julio Pascual
María José Pérez-Sáez
Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
description Early hypertransaminasemia after kidney transplantation (KT) is frequent. It has been associated with the crosstalk produced between the liver and the kidney in ischemia-reperfusion situations. However, the influence of the donor type has not been evaluated. We present a retrospective study analyzing the increase in serum aspartate aminotransferase/alanine aminotransferase (AST/ALT) during the first three months post-KT in 151 recipients who received thymoglobulin as induction therapy, either from brain-death donors (DBD, <i>n</i> = 75), controlled circulatory death donors (cDCD, <i>n</i> = 33), or uncontrolled DCD (uDCD, <i>n</i> = 43). Eighty-five KT recipients from DBD who received basiliximab were included as controls. From KT recipients who received thymoglobulin, 33.6/43.4% presented with an increase in AST/ALT at 72 h post-KT, respectively. Regarding donor type, the percentage of recipients who experienced 72 h post-KT hypertransaminasemia was higher in uDCD group (65.1/83.7% vs. 20.3/26% in DBD and 20.7/27.6% in cDCD, <i>p</i> < 0.001). Within the control group, 9.4/12.9% of patients presented with AST/ALT elevation. One month after transplant, AST/ALT values returned to baseline in all groups. The multivariate analysis showed that uDCD recipients had 6- to 12-fold higher risk of developing early post-KT hypertransaminasemia. Early post-KT hypertransaminasemia is a frequent and transient event related to the kidney donor type, being more frequent in uDCD recipients.
format article
author Eulàlia Solà-Porta
Dolores Redondo-Pachón
Carlos Arias-Cabrales
Diego Navazo
Anna Buxeda
Carla Burballa
Marta Crespo
Montserrat García-Retortillo
Julio Pascual
María José Pérez-Sáez
author_facet Eulàlia Solà-Porta
Dolores Redondo-Pachón
Carlos Arias-Cabrales
Diego Navazo
Anna Buxeda
Carla Burballa
Marta Crespo
Montserrat García-Retortillo
Julio Pascual
María José Pérez-Sáez
author_sort Eulàlia Solà-Porta
title Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title_short Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title_full Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title_fullStr Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title_full_unstemmed Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title_sort early hypertransaminasemia after kidney transplantation: significance and evolution according to donor type
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/7a4be361c9744bb2bc3df7fa2a9703d7
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