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The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation

The effective calcineurin inhibitor (CNI) tacrolimus (Tac) is an integral part of the standard immunosuppressive regimen after renal transplantation (RTx). However, as a potent CNI it has nephrotoxic potential leading to impaired renal function in some cases. Therefore, it is of high clinical impact...

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Autores principales: Thölking, Gerold, Fortmann, Christian, Koch, Raphael, Gerth, Hans Ulrich, Pabst, Dirk, Pavenstädt, Hermann, Kabar, Iyad, Hüsing, Anna, Wolters, Heiner, Reuter, Stefan, Suwelack, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207775/
https://www.ncbi.nlm.nih.gov/pubmed/25340655
http://dx.doi.org/10.1371/journal.pone.0111128
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author Thölking, Gerold
Fortmann, Christian
Koch, Raphael
Gerth, Hans Ulrich
Pabst, Dirk
Pavenstädt, Hermann
Kabar, Iyad
Hüsing, Anna
Wolters, Heiner
Reuter, Stefan
Suwelack, Barbara
author_facet Thölking, Gerold
Fortmann, Christian
Koch, Raphael
Gerth, Hans Ulrich
Pabst, Dirk
Pavenstädt, Hermann
Kabar, Iyad
Hüsing, Anna
Wolters, Heiner
Reuter, Stefan
Suwelack, Barbara
author_sort Thölking, Gerold
collection PubMed
description The effective calcineurin inhibitor (CNI) tacrolimus (Tac) is an integral part of the standard immunosuppressive regimen after renal transplantation (RTx). However, as a potent CNI it has nephrotoxic potential leading to impaired renal function in some cases. Therefore, it is of high clinical impact to identify factors which can predict who is endangered to develop CNI toxicity. We hypothesized that the Tac metabolism rate expressed as the blood concentration normalized by the dose (C/D ratio) is such a simple predictor. Therefore, we analyzed the impact of the C/D ratio on kidney function after RTx. Renal function was analyzed 1, 2, 3, 6, 12 and 24 months after RTx in 248 patients with an immunosuppressive regimen including basiliximab, tacrolimus, mycophenolate mofetil and prednisolone. According to keep the approach simple, patients were split into three C/D groups: fast, intermediate and slow metabolizers. Notably, compared with slow metabolizers fast metabolizers of Tac showed significantly lower estimated glomerular filtration rate (eGFR) values at all the time points analyzed. Moreover, fast metabolizers underwent more indication renal biopsies (p = 0.006) which revealed a higher incidence of CNI nephrotoxicity (p = 0.015) and BK nephropathy (p = 0.024) in this group. We herein identified the C/D ratio as an easy calculable risk factor for the development of CNI nephrotoxicity and BK nephropathy after RTx. We propose that the simple C/D ratio should be taken into account early in patient’s risk management strategies.
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spelling pubmed-42077752014-10-27 The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation Thölking, Gerold Fortmann, Christian Koch, Raphael Gerth, Hans Ulrich Pabst, Dirk Pavenstädt, Hermann Kabar, Iyad Hüsing, Anna Wolters, Heiner Reuter, Stefan Suwelack, Barbara PLoS One Research Article The effective calcineurin inhibitor (CNI) tacrolimus (Tac) is an integral part of the standard immunosuppressive regimen after renal transplantation (RTx). However, as a potent CNI it has nephrotoxic potential leading to impaired renal function in some cases. Therefore, it is of high clinical impact to identify factors which can predict who is endangered to develop CNI toxicity. We hypothesized that the Tac metabolism rate expressed as the blood concentration normalized by the dose (C/D ratio) is such a simple predictor. Therefore, we analyzed the impact of the C/D ratio on kidney function after RTx. Renal function was analyzed 1, 2, 3, 6, 12 and 24 months after RTx in 248 patients with an immunosuppressive regimen including basiliximab, tacrolimus, mycophenolate mofetil and prednisolone. According to keep the approach simple, patients were split into three C/D groups: fast, intermediate and slow metabolizers. Notably, compared with slow metabolizers fast metabolizers of Tac showed significantly lower estimated glomerular filtration rate (eGFR) values at all the time points analyzed. Moreover, fast metabolizers underwent more indication renal biopsies (p = 0.006) which revealed a higher incidence of CNI nephrotoxicity (p = 0.015) and BK nephropathy (p = 0.024) in this group. We herein identified the C/D ratio as an easy calculable risk factor for the development of CNI nephrotoxicity and BK nephropathy after RTx. We propose that the simple C/D ratio should be taken into account early in patient’s risk management strategies. Public Library of Science 2014-10-23 /pmc/articles/PMC4207775/ /pubmed/25340655 http://dx.doi.org/10.1371/journal.pone.0111128 Text en © 2014 Thölking et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Thölking, Gerold
Fortmann, Christian
Koch, Raphael
Gerth, Hans Ulrich
Pabst, Dirk
Pavenstädt, Hermann
Kabar, Iyad
Hüsing, Anna
Wolters, Heiner
Reuter, Stefan
Suwelack, Barbara
The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title_full The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title_fullStr The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title_full_unstemmed The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title_short The Tacrolimus Metabolism Rate Influences Renal Function after Kidney Transplantation
title_sort tacrolimus metabolism rate influences renal function after kidney transplantation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207775/
https://www.ncbi.nlm.nih.gov/pubmed/25340655
http://dx.doi.org/10.1371/journal.pone.0111128
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