Literature DB >> 21168674

Proton pump inhibitor co-medication reduces active drug exposure in heart transplant recipients receiving mycophenolate mofetil.

A O Doesch1, S Mueller, M Konstandin, S Celik, C Erbel, A Kristen, L Frankenstein, A Koch, P Ehlermann, C Zugck, H A Katus.   

Abstract

BACKGROUND: Proton pump inhibitors (PPIs) are often prescribed for gastrointestinal discomfort after heart transplantation. This study investigated the impact of PPI use on mycophenolic acid (MPA) pharmacokinetics in heart transplant recipients receiving mycophenolate mofetil (MMF) in combination with a calcineurin inhibitor (tacrolimus [TAC]/cyclosporine [CsA]) or mammalian target of rapamycin inhibitor (sirolimus/everolimus).
METHODS: Abbreviated MPA areas under the curve (AUCs; 0, 30, and 120 minutes after morning intake) were obtained in 19 patients on a PPI (initial examination) and 1 month after PPI discontinuation (follow-up). Mean patient age was 58.2 ± 8.8 years, and mean time after transplantation was 2.3 ± 4.0 years (range, 0.2-13.0 years).
RESULTS: At initial examination mean daily MMF dose was 2.2 ± 0.8 g. MMF dose was kept unchanged for the duration of study (P = ns). Mean predose (C0) MPA serum concentrations were insignificantly lower with PPI comedication (2.5 ± 2.2 mg/L vs 2.8 ± 1.7 mg/L; P = .15). Dose-adjusted abbreviated MPA AUCs (adjusted to morning dose) were significantly lower during PPI therapy (45.2 ± 20.3 vs 65.2 ± 38.8 mg·h/L·g [MMF]; P = .02).
CONCLUSIONS: Patients with PPI comedication during MMF therapy show significantly lower exposure to mycophenolic acid determined by dose-adjusted abbreviated MPA AUCs. Although the clinical relevance of this pharmacokinetic interaction was not determined in this study, MPA drug monitoring by limited sampling strategies might be helpful during changes in antacid comedication in patients on MMF.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21168674     DOI: 10.1016/j.transproceed.2010.09.047

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  5 in total

1.  No relevant pharmacokinetic interaction between pantoprazole and mycophenolate in renal transplant patients: a randomized crossover study.

Authors:  Olesja Rissling; Petra Glander; Pia Hambach; Marco Mai; Susanne Brakemeier; Daniela Klonower; Fabian Halleck; Eugenia Singer; Eva-Vanessa Schrezenmeier; Michael Dürr; Hans-Hellmut Neumayer; Klemens Budde
Journal:  Br J Clin Pharmacol       Date:  2015-07-14       Impact factor: 4.335

Review 2.  Clinical pharmacokinetics and pharmacodynamics of mycophenolate in patients with autoimmune disease.

Authors:  Azrin N Abd Rahman; Susan E Tett; Christine E Staatz
Journal:  Clin Pharmacokinet       Date:  2013-05       Impact factor: 6.447

3.  Pharmacokinetic drug interaction profile of omeprazole with adverse consequences and clinical risk management.

Authors:  Wei Li; Su Zeng; Lu-Shan Yu; Quan Zhou
Journal:  Ther Clin Risk Manag       Date:  2013-05-27       Impact factor: 2.423

4.  Pantoprazole Does not Affect Serum Trough Levels of Tacrolimus and Everolimus in Liver Transplant Recipients.

Authors:  Sebastian C B Bremer; Lars Reinhardt; Michael Sobotta; Marie C Hasselluhn; Thomas Lorf; Volker Ellenrieder; Harald Schwörer
Journal:  Front Med (Lausanne)       Date:  2018-11-19

5.  Different Routes of Proton Pumps Inhibitors Co-Administration have Significant Impact on Mycophenolate Acid (MPA) Serum Levels in Heart Transplant Recipients.

Authors:  Tomasz Urbanowicz; Ewa Straburzyńska-Migaj; Veronica Casadei; Michał Bociański; Marek Jemielity
Journal:  Ann Transplant       Date:  2020-01-24       Impact factor: 1.530

  5 in total

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