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Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose

BACKGROUND: Bodyweight-based dosing of tacrolimus (Tac) is considered standard care, even though the available evidence is thin. An increasing proportion of transplant recipients is overweight, prompting the question if the starting dose should always be based on bodyweight. METHODS: For this analys...

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Autores principales: Andrews, Louise M., de Winter, Brenda C.M., Tang, Jiang-Tao, Shuker, Nauras, Bouamar, Rachida, van Schaik, Ron H.N., Koch, Birgit C.P., van Gelder, Teun, Hesselink, Dennis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367746/
https://www.ncbi.nlm.nih.gov/pubmed/28361113
http://dx.doi.org/10.1097/TXD.0000000000000644
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author Andrews, Louise M.
de Winter, Brenda C.M.
Tang, Jiang-Tao
Shuker, Nauras
Bouamar, Rachida
van Schaik, Ron H.N.
Koch, Birgit C.P.
van Gelder, Teun
Hesselink, Dennis A.
author_facet Andrews, Louise M.
de Winter, Brenda C.M.
Tang, Jiang-Tao
Shuker, Nauras
Bouamar, Rachida
van Schaik, Ron H.N.
Koch, Birgit C.P.
van Gelder, Teun
Hesselink, Dennis A.
author_sort Andrews, Louise M.
collection PubMed
description BACKGROUND: Bodyweight-based dosing of tacrolimus (Tac) is considered standard care, even though the available evidence is thin. An increasing proportion of transplant recipients is overweight, prompting the question if the starting dose should always be based on bodyweight. METHODS: For this analysis, data were used from a randomized-controlled trial in which patients received either a standard Tac starting dose or a dose that was based on CYP3A5 genotype. The hypothesis was that overweight patients would have Tac overexposure following standard bodyweight-based dosing. RESULTS: Data were available for 203 kidney transplant recipients, with a median body mass index (BMI) of 25.6 (range, 17.2-42.2). More than 50% of the overweight or obese patients had a Tac predose concentration above the target range. The CYP3A5 nonexpressers tended to be above target when they weighed more than 67.5 kg or had a BMI of 24.5 or higher. Dosing guidelines were proposed with a decrease up to 40% in Tac starting doses for different BMI groups. The dosing guideline for patients with an unknown genotype was validated using the fixed-dose versus concentration controlled data set. CONCLUSIONS: This study demonstrates that dosing Tac solely on bodyweight results in overexposure in more than half of overweight or obese patients.
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spelling pubmed-53677462017-03-30 Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose Andrews, Louise M. de Winter, Brenda C.M. Tang, Jiang-Tao Shuker, Nauras Bouamar, Rachida van Schaik, Ron H.N. Koch, Birgit C.P. van Gelder, Teun Hesselink, Dennis A. Transplant Direct Pharmacology BACKGROUND: Bodyweight-based dosing of tacrolimus (Tac) is considered standard care, even though the available evidence is thin. An increasing proportion of transplant recipients is overweight, prompting the question if the starting dose should always be based on bodyweight. METHODS: For this analysis, data were used from a randomized-controlled trial in which patients received either a standard Tac starting dose or a dose that was based on CYP3A5 genotype. The hypothesis was that overweight patients would have Tac overexposure following standard bodyweight-based dosing. RESULTS: Data were available for 203 kidney transplant recipients, with a median body mass index (BMI) of 25.6 (range, 17.2-42.2). More than 50% of the overweight or obese patients had a Tac predose concentration above the target range. The CYP3A5 nonexpressers tended to be above target when they weighed more than 67.5 kg or had a BMI of 24.5 or higher. Dosing guidelines were proposed with a decrease up to 40% in Tac starting doses for different BMI groups. The dosing guideline for patients with an unknown genotype was validated using the fixed-dose versus concentration controlled data set. CONCLUSIONS: This study demonstrates that dosing Tac solely on bodyweight results in overexposure in more than half of overweight or obese patients. Lippincott Williams & Wilkins 2017-01-19 /pmc/articles/PMC5367746/ /pubmed/28361113 http://dx.doi.org/10.1097/TXD.0000000000000644 Text en Copyright © 2017 The Authors. Transplantation Direct. Published by Wolters Kluwer Health, Inc. 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) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , 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.
spellingShingle Pharmacology
Andrews, Louise M.
de Winter, Brenda C.M.
Tang, Jiang-Tao
Shuker, Nauras
Bouamar, Rachida
van Schaik, Ron H.N.
Koch, Birgit C.P.
van Gelder, Teun
Hesselink, Dennis A.
Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title_full Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title_fullStr Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title_full_unstemmed Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title_short Overweight Kidney Transplant Recipients Are at Risk of Being Overdosed Following Standard Bodyweight-Based Tacrolimus Starting Dose
title_sort overweight kidney transplant recipients are at risk of being overdosed following standard bodyweight-based tacrolimus starting dose
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367746/
https://www.ncbi.nlm.nih.gov/pubmed/28361113
http://dx.doi.org/10.1097/TXD.0000000000000644
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