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Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation

Background: The calcineurin inhibitor (CNI) tacrolimus (TAC) is a cornerstone agent in immunosuppressive therapy in pediatric liver transplantation (LTX). Adverse effects limit the use of CNI. In adults, calculating the individual TAC metabolism rate allows to estimate the transplant recipient'...

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Autores principales: Prusinskas, Benas, Ohlsson, Sinja, Kathemann, Simone, Pilic, Denisa, Kampmann, Kristina, Büscher, Rainer, Paul, Andreas, Pape, Lars, Hoyer, Peter F., Lainka, Elke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206534/
https://www.ncbi.nlm.nih.gov/pubmed/34150686
http://dx.doi.org/10.3389/fped.2021.659608
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author Prusinskas, Benas
Ohlsson, Sinja
Kathemann, Simone
Pilic, Denisa
Kampmann, Kristina
Büscher, Rainer
Paul, Andreas
Pape, Lars
Hoyer, Peter F.
Lainka, Elke
author_facet Prusinskas, Benas
Ohlsson, Sinja
Kathemann, Simone
Pilic, Denisa
Kampmann, Kristina
Büscher, Rainer
Paul, Andreas
Pape, Lars
Hoyer, Peter F.
Lainka, Elke
author_sort Prusinskas, Benas
collection PubMed
description Background: The calcineurin inhibitor (CNI) tacrolimus (TAC) is a cornerstone agent in immunosuppressive therapy in pediatric liver transplantation (LTX). Adverse effects limit the use of CNI. In adults, calculating the individual TAC metabolism rate allows to estimate the transplant recipient's risk for therapy-associated complications. Methods: A retrospective, descriptive data analysis was performed in children who had undergone LTX in 2009–2017 and had received TAC twice daily in the first year after LTX. A weight-adjusted concentration/dose ratio (C/D ratio) was calculated [TAC trough level/(daily TAC dose/body weight)] every 3 months after LTX to estimate the average individual TAC metabolism rate. Depending on the C/D ratio, all patients were divided into two groups: fast metabolizers (FM) and slow metabolizers (SM). Clinical and laboratory parameters were analyzed as risk factors in both groups. Results: A total of 78 children (w 34, m 44, median age at LTX 2.4; 0.4–17.0 years) were enrolled in the study. FM (SM) had a mean C/D ratio of <51.83 (≥51.83) ng/ml/(mg/kg). FM were younger at the time of LTX (median age 1.7; 0.4–15.8 years) than SM (5.1, 0.4–17.0), p = 0.008. FM were more likely to have biliary atresia (20/39, 51%) compared to SM (11/39, 28%), p = 0.038, whereas SM were more likely to have progressive familial intrahepatic cholestasis (9/39, 23%) vs. in FM (1/39, 3%), p = 0.014. Epstein–Barr virus (EBV) infection occurred more frequently in FM (27/39, 69%) than SM (13/39, 33%), p = 0.002. Three FM developed post-transplant lymphoproliferative disorder. The annual change of renal function did not differ in both groups (slope FM 1.2 ± 0.6; SM 1.4 ± 0.8 ml/min/1.73 m(2) per year, and p = 0.841). Conclusions: Calculation of individual, weight-adjusted TAC C/D ratio is a simple, effective, and cost-efficient tool for physicians to estimate the risk of therapy-associated complications and to initiate individual preventive adjustments after pediatric LTX. Lower TAC levels are tolerable in FM, especially in the presence of EBV infection, reduced renal function, or when receiving a liver transplant in the first 2 years of life.
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spelling pubmed-82065342021-06-17 Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation Prusinskas, Benas Ohlsson, Sinja Kathemann, Simone Pilic, Denisa Kampmann, Kristina Büscher, Rainer Paul, Andreas Pape, Lars Hoyer, Peter F. Lainka, Elke Front Pediatr Pediatrics Background: The calcineurin inhibitor (CNI) tacrolimus (TAC) is a cornerstone agent in immunosuppressive therapy in pediatric liver transplantation (LTX). Adverse effects limit the use of CNI. In adults, calculating the individual TAC metabolism rate allows to estimate the transplant recipient's risk for therapy-associated complications. Methods: A retrospective, descriptive data analysis was performed in children who had undergone LTX in 2009–2017 and had received TAC twice daily in the first year after LTX. A weight-adjusted concentration/dose ratio (C/D ratio) was calculated [TAC trough level/(daily TAC dose/body weight)] every 3 months after LTX to estimate the average individual TAC metabolism rate. Depending on the C/D ratio, all patients were divided into two groups: fast metabolizers (FM) and slow metabolizers (SM). Clinical and laboratory parameters were analyzed as risk factors in both groups. Results: A total of 78 children (w 34, m 44, median age at LTX 2.4; 0.4–17.0 years) were enrolled in the study. FM (SM) had a mean C/D ratio of <51.83 (≥51.83) ng/ml/(mg/kg). FM were younger at the time of LTX (median age 1.7; 0.4–15.8 years) than SM (5.1, 0.4–17.0), p = 0.008. FM were more likely to have biliary atresia (20/39, 51%) compared to SM (11/39, 28%), p = 0.038, whereas SM were more likely to have progressive familial intrahepatic cholestasis (9/39, 23%) vs. in FM (1/39, 3%), p = 0.014. Epstein–Barr virus (EBV) infection occurred more frequently in FM (27/39, 69%) than SM (13/39, 33%), p = 0.002. Three FM developed post-transplant lymphoproliferative disorder. The annual change of renal function did not differ in both groups (slope FM 1.2 ± 0.6; SM 1.4 ± 0.8 ml/min/1.73 m(2) per year, and p = 0.841). Conclusions: Calculation of individual, weight-adjusted TAC C/D ratio is a simple, effective, and cost-efficient tool for physicians to estimate the risk of therapy-associated complications and to initiate individual preventive adjustments after pediatric LTX. Lower TAC levels are tolerable in FM, especially in the presence of EBV infection, reduced renal function, or when receiving a liver transplant in the first 2 years of life. Frontiers Media S.A. 2021-06-02 /pmc/articles/PMC8206534/ /pubmed/34150686 http://dx.doi.org/10.3389/fped.2021.659608 Text en Copyright © 2021 Prusinskas, Ohlsson, Kathemann, Pilic, Kampmann, Büscher, Paul, Pape, Hoyer and Lainka. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Prusinskas, Benas
Ohlsson, Sinja
Kathemann, Simone
Pilic, Denisa
Kampmann, Kristina
Büscher, Rainer
Paul, Andreas
Pape, Lars
Hoyer, Peter F.
Lainka, Elke
Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title_full Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title_fullStr Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title_full_unstemmed Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title_short Role of Tacrolimus C/D Ratio in the First Year After Pediatric Liver Transplantation
title_sort role of tacrolimus c/d ratio in the first year after pediatric liver transplantation
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206534/
https://www.ncbi.nlm.nih.gov/pubmed/34150686
http://dx.doi.org/10.3389/fped.2021.659608
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