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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
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. |
format | Online Article Text |
id | pubmed-8584479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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