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The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation
Early allograft dysfunction (EAD) is considered a precursor to graft loss in liver transplantation. To date, the use of preoperative serum cytokine profiles to predict EAD development has not been systematically investigated in living donor liver transplantation (LDLT). Here, we investigated the ass...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916661/ https://www.ncbi.nlm.nih.gov/pubmed/29668595 http://dx.doi.org/10.1097/MD.0000000000010400 |
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author | Chae, Min Suk Kim, Jong-Woan Chung, Hyun Sik Park, Chul Soo Lee, Jaemin Choi, Jong Ho Hong, Sang Hyun |
author_facet | Chae, Min Suk Kim, Jong-Woan Chung, Hyun Sik Park, Chul Soo Lee, Jaemin Choi, Jong Ho Hong, Sang Hyun |
author_sort | Chae, Min Suk |
collection | PubMed |
description | Early allograft dysfunction (EAD) is considered a precursor to graft loss in liver transplantation. To date, the use of preoperative serum cytokine profiles to predict EAD development has not been systematically investigated in living donor liver transplantation (LDLT). Here, we investigated the association between preoperative serum cytokine profiles and EAD development in LDLT patients. Serum cytokine profiles collected preoperatively and on postoperative day 7 were retrospectively reviewed. The specific serum cytokines analyzed included interleukin (IL)-2, IL-6, IL-10, IL-12, IL-17, interferon (IFN)-γ, and tumor necrosis factor (TNF)-α. The cytokine levels of patients with EAD were compared with those of patients without EAD and the impact of cytokine levels on the occurrence of EAD was evaluated. Preoperatively, the serum levels of IL-6, 10, 17, and TNF-α were significantly higher in the EAD group than in the non-EAD group. In univariate logistic analysis, the preoperative levels of IL-6, IL-10, IL-17, IFN-γ, and TNF-α were potentially associated with EAD development. After multivariate logistic analysis, higher preoperative serum levels of IL-6 and 17 were significantly associated with EAD development. In addition, the incidence of EAD increased as the preoperative serum levels of IL-6 and IL-17 increased. Preoperative serum levels of IL-6 and IL-17 were significantly associated with EAD development in LDLT. |
format | Online Article Text |
id | pubmed-5916661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-59166612018-05-01 The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation Chae, Min Suk Kim, Jong-Woan Chung, Hyun Sik Park, Chul Soo Lee, Jaemin Choi, Jong Ho Hong, Sang Hyun Medicine (Baltimore) 3300 Early allograft dysfunction (EAD) is considered a precursor to graft loss in liver transplantation. To date, the use of preoperative serum cytokine profiles to predict EAD development has not been systematically investigated in living donor liver transplantation (LDLT). Here, we investigated the association between preoperative serum cytokine profiles and EAD development in LDLT patients. Serum cytokine profiles collected preoperatively and on postoperative day 7 were retrospectively reviewed. The specific serum cytokines analyzed included interleukin (IL)-2, IL-6, IL-10, IL-12, IL-17, interferon (IFN)-γ, and tumor necrosis factor (TNF)-α. The cytokine levels of patients with EAD were compared with those of patients without EAD and the impact of cytokine levels on the occurrence of EAD was evaluated. Preoperatively, the serum levels of IL-6, 10, 17, and TNF-α were significantly higher in the EAD group than in the non-EAD group. In univariate logistic analysis, the preoperative levels of IL-6, IL-10, IL-17, IFN-γ, and TNF-α were potentially associated with EAD development. After multivariate logistic analysis, higher preoperative serum levels of IL-6 and 17 were significantly associated with EAD development. In addition, the incidence of EAD increased as the preoperative serum levels of IL-6 and IL-17 increased. Preoperative serum levels of IL-6 and IL-17 were significantly associated with EAD development in LDLT. Wolters Kluwer Health 2018-04-20 /pmc/articles/PMC5916661/ /pubmed/29668595 http://dx.doi.org/10.1097/MD.0000000000010400 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | 3300 Chae, Min Suk Kim, Jong-Woan Chung, Hyun Sik Park, Chul Soo Lee, Jaemin Choi, Jong Ho Hong, Sang Hyun The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title | The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title_full | The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title_fullStr | The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title_full_unstemmed | The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title_short | The impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
title_sort | impact of serum cytokines in the development of early allograft dysfunction in living donor liver transplantation |
topic | 3300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916661/ https://www.ncbi.nlm.nih.gov/pubmed/29668595 http://dx.doi.org/10.1097/MD.0000000000010400 |
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