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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: Solà-Porta, Eulàlia, Redondo-Pachón, Dolores, Arias-Cabrales, Carlos, Navazo, Diego, Buxeda, Anna, Burballa, Carla, Crespo, Marta, García-Retortillo, Montserrat, Pascual, Julio, Pérez-Sáez, María José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584479/
https://www.ncbi.nlm.nih.gov/pubmed/34768688
http://dx.doi.org/10.3390/jcm10215168
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author Solà-Porta, Eulàlia
Redondo-Pachón, Dolores
Arias-Cabrales, Carlos
Navazo, Diego
Buxeda, Anna
Burballa, Carla
Crespo, Marta
García-Retortillo, Montserrat
Pascual, Julio
Pérez-Sáez, María José
author_facet Solà-Porta, Eulàlia
Redondo-Pachón, Dolores
Arias-Cabrales, Carlos
Navazo, Diego
Buxeda, Anna
Burballa, Carla
Crespo, Marta
García-Retortillo, Montserrat
Pascual, Julio
Pérez-Sáez, María José
author_sort Solà-Porta, Eulàlia
collection PubMed
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, n = 75), controlled circulatory death donors (cDCD, n = 33), or uncontrolled DCD (uDCD, n = 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, p < 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.
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spelling pubmed-85844792021-11-12 Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type Solà-Porta, Eulàlia Redondo-Pachón, Dolores Arias-Cabrales, Carlos Navazo, Diego Buxeda, Anna Burballa, Carla Crespo, Marta García-Retortillo, Montserrat Pascual, Julio Pérez-Sáez, María José J Clin Med Article 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, n = 75), controlled circulatory death donors (cDCD, n = 33), or uncontrolled DCD (uDCD, n = 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, p < 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. MDPI 2021-11-04 /pmc/articles/PMC8584479/ /pubmed/34768688 http://dx.doi.org/10.3390/jcm10215168 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Solà-Porta, Eulàlia
Redondo-Pachón, Dolores
Arias-Cabrales, Carlos
Navazo, Diego
Buxeda, Anna
Burballa, Carla
Crespo, Marta
García-Retortillo, Montserrat
Pascual, Julio
Pérez-Sáez, María José
Early Hypertransaminasemia after Kidney Transplantation: Significance and Evolution According to Donor Type
title 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_short 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
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584479/
https://www.ncbi.nlm.nih.gov/pubmed/34768688
http://dx.doi.org/10.3390/jcm10215168
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