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Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation
Immunosuppression is the major risk factor for BK virus nephropathy (BKVN) after renal transplantation (RTx). As the individual tacrolimus (Tac) metabolism rate correlates with Tac side effects, we hypothesized that Tac metabolism might also influence the BKV infection risk. In this case-control stu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004181/ https://www.ncbi.nlm.nih.gov/pubmed/27573493 http://dx.doi.org/10.1038/srep32273 |
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author | Thölking, Gerold Schmidt, Christina Koch, Raphael Schuette-Nuetgen, Katharina Pabst, Dirk Wolters, Heiner Kabar, Iyad Hüsing, Anna Pavenstädt, Hermann Reuter, Stefan Suwelack, Barbara |
author_facet | Thölking, Gerold Schmidt, Christina Koch, Raphael Schuette-Nuetgen, Katharina Pabst, Dirk Wolters, Heiner Kabar, Iyad Hüsing, Anna Pavenstädt, Hermann Reuter, Stefan Suwelack, Barbara |
author_sort | Thölking, Gerold |
collection | PubMed |
description | Immunosuppression is the major risk factor for BK virus nephropathy (BKVN) after renal transplantation (RTx). As the individual tacrolimus (Tac) metabolism rate correlates with Tac side effects, we hypothesized that Tac metabolism might also influence the BKV infection risk. In this case-control study RTx patients with BK viremia within 4 years after RTx (BKV group) were compared with a BKV negative control group. The Tac metabolism rate expressed as the blood concentration normalized by the daily dose (C/D ratio) was applied to assess the Tac metabolism rate. BK viremia was detected in 86 patients after a median time of 6 (0–36) months after RTx. BKV positive patients showed lower Tac C/D ratios at 1, 3 and 6 months after RTx and were classified as fast Tac metabolizers. 8 of 86 patients with BK viremia had histologically proven BKN and a higher median maximum viral load than BKV patients without BKN (441,000 vs. 18,572 copies/mL). We conclude from our data that fast Tac metabolism (C/D ratio <1.05) is associated with BK viremia after RTx. Calculation of the Tac C/D ratio early after RTx, may assist transplant clinicians to identify patients at risk and to choose the optimal immunosuppressive regimen. |
format | Online Article Text |
id | pubmed-5004181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50041812016-09-07 Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation Thölking, Gerold Schmidt, Christina Koch, Raphael Schuette-Nuetgen, Katharina Pabst, Dirk Wolters, Heiner Kabar, Iyad Hüsing, Anna Pavenstädt, Hermann Reuter, Stefan Suwelack, Barbara Sci Rep Article Immunosuppression is the major risk factor for BK virus nephropathy (BKVN) after renal transplantation (RTx). As the individual tacrolimus (Tac) metabolism rate correlates with Tac side effects, we hypothesized that Tac metabolism might also influence the BKV infection risk. In this case-control study RTx patients with BK viremia within 4 years after RTx (BKV group) were compared with a BKV negative control group. The Tac metabolism rate expressed as the blood concentration normalized by the daily dose (C/D ratio) was applied to assess the Tac metabolism rate. BK viremia was detected in 86 patients after a median time of 6 (0–36) months after RTx. BKV positive patients showed lower Tac C/D ratios at 1, 3 and 6 months after RTx and were classified as fast Tac metabolizers. 8 of 86 patients with BK viremia had histologically proven BKN and a higher median maximum viral load than BKV patients without BKN (441,000 vs. 18,572 copies/mL). We conclude from our data that fast Tac metabolism (C/D ratio <1.05) is associated with BK viremia after RTx. Calculation of the Tac C/D ratio early after RTx, may assist transplant clinicians to identify patients at risk and to choose the optimal immunosuppressive regimen. Nature Publishing Group 2016-08-30 /pmc/articles/PMC5004181/ /pubmed/27573493 http://dx.doi.org/10.1038/srep32273 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Thölking, Gerold Schmidt, Christina Koch, Raphael Schuette-Nuetgen, Katharina Pabst, Dirk Wolters, Heiner Kabar, Iyad Hüsing, Anna Pavenstädt, Hermann Reuter, Stefan Suwelack, Barbara Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title | Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title_full | Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title_fullStr | Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title_full_unstemmed | Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title_short | Influence of tacrolimus metabolism rate on BKV infection after kidney transplantation |
title_sort | influence of tacrolimus metabolism rate on bkv infection after kidney transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5004181/ https://www.ncbi.nlm.nih.gov/pubmed/27573493 http://dx.doi.org/10.1038/srep32273 |
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