Literature DB >> 30252957

High tacrolimus clearance - a risk factor for development of interstitial fibrosis and tubular atrophy in the transplanted kidney: a retrospective single-center cohort study.

Erlend Johannessen Egeland1, Anna Varberg Reisaeter2, Ida Robertsen1, Karsten Midtvedt2, Erik Heyerdahl Strøm3, Hallvard Holdaas2, Anders Hartmann2, Anders Åsberg1,2.   

Abstract

Patients with high tacrolimus clearance are more likely to experience transient under-immunosuppression in case of a missed or delayed dose. We wanted to investigate the association between estimated tacrolimus clearance and development of graft interstitial fibrosis and tubular atrophy (IFTA) in kidney transplant recipients. Associations between estimated tacrolimus clearance [daily tacrolimus dose (mg)/trough concentration (μg/l)] and changes in IFTA biopsy scores from week 7 to 1-year post-transplantation were investigated. Data from 504 patients transplanted between 2009 and 2013 with paired protocol biopsies (7 weeks + 1-year post-transplant) were included. There were no differences in baseline biopsy scores (7 weeks) in patients with different estimated tacrolimus clearance. Increasing tacrolimus clearance was significantly associated with increased ci + ct score of ≥2 at 1 year, odds ratio of 1.67 (95% CI; 1.11-2.51). In patients without fibrosis (ci + ct ≤ 1) at 7 weeks (n = 233), increasing tacrolimus clearance was associated with development of de novo IFTA (i + t ≤ 1 and ci + ct ≥ 2) at 1 year, odds ratio of 2.01 (95% CI; 1.18-3.50) after adjusting for confounders. High tacrolimus clearance was significantly associated with development of IFTA the first year following renal transplantation.
© 2018 Steunstichting ESOT.

Entities:  

Keywords:  interstitial fibrosis and tubular atrophy; nephrotoxicity; pharmacokinetics; tacrolimus

Mesh:

Substances:

Year:  2018        PMID: 30252957     DOI: 10.1111/tri.13356

Source DB:  PubMed          Journal:  Transpl Int        ISSN: 0934-0874            Impact factor:   3.782


  5 in total

Review 1.  Comparison of the Impact of Pharmacogenetic Variability on the PK of Slow Release and Immediate Release Tacrolimus Formulations.

Authors:  Teun van Gelder; Oumaima Etsouli; Dirk Jan Moes; Jesse J Swen
Journal:  Genes (Basel)       Date:  2020-10-15       Impact factor: 4.096

2.  Improved Kidney Allograft Function after Early Conversion of Fast IR-Tac Metabolizers to LCP-Tac.

Authors:  Gerold Thölking; Filiz Tosun-Koç; Ulrich Jehn; Raphael Koch; Hermann Pavenstädt; Barbara Suwelack; Stefan Reuter
Journal:  J Clin Med       Date:  2022-02-26       Impact factor: 4.241

3.  A Low Tacrolimus Concentration/Dose Ratio Increases the Risk for the Development of Acute Calcineurin Inhibitor-Induced Nephrotoxicity.

Authors:  Gerold Thölking; Katharina Schütte-Nütgen; Julia Schmitz; Alexandros Rovas; Maximilian Dahmen; Joachim Bautz; Ulrich Jehn; Hermann Pavenstädt; Barbara Heitplatz; Veerle Van Marck; Barbara Suwelack; Stefan Reuter
Journal:  J Clin Med       Date:  2019-10-02       Impact factor: 4.241

4.  Conversion to Everolimus was Beneficial and Safe for Fast and Slow Tacrolimus Metabolizers After Renal Transplantation.

Authors:  Gerold Thölking; Nils Hendrik Gillhaus; Katharina Schütte-Nütgen; Hermann Pavenstädt; Raphael Koch; Barbara Suwelack; Stefan Reuter
Journal:  J Clin Med       Date:  2020-01-23       Impact factor: 4.241

5.  Increased renal function decline in fast metabolizers using extended-release tacrolimus after kidney transplantation.

Authors:  Stefan Reuter; Dirk Kuypers; Gerold Thölking; Brigitte Filensky; Ulrich Jehn; Katharina Schütte-Nütgen; Raphael Koch; Christine Kurschat; Hermann Pavenstädt; Barbara Suwelack
Journal:  Sci Rep       Date:  2021-08-02       Impact factor: 4.379

  5 in total

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