Lansoprazole—Tacrolimus Interaction in Japanese Transplant Recipient with CYP2C19 Polymorphism

Author:

Takahashi Kazushige1,Motohashi Hideyuki2,Yonezawa Atsushi3,Okuda Masahiro4,Ito Noriyuki5,Yamamoto Shingo6,Ogawa Osamu7,Inui Ken-ichi8

Affiliation:

1. Kazushige Takahashi MS, Pharmacist, Department of Pharmacy, Kyoto University Hospital; Faculty of Medicine, Kyoto University, Kyoto, Japan

2. Hideyuki Motohashi PhD, Research Associate, Department of Pharmacy, Kyoto University Hospital; Faculty of Medicine, Kyoto University

3. Atsushi Yonezawa BS, Department of Pharmacy, Kyoto University Hospital; Faculty of Medicine, Kyoto University

4. Masahiro Okuda PhD, Associate Professor, Department of Pharmacy, Kyoto University Hospital; Faculty of Medicine, Kyoto University

5. Noriyuki Ito MD, Lecturer, Pharmacist, Department of Urology, Graduate School of Medicine, Kyoto University

6. Shingo Yamamoto MD, Associate Professor, Department of Urology, Graduate School of Medicine, Kyoto University

7. Osamu Ogawa MD, Professor and Chairman, Department of Urology, Graduate School of Medicine, Kyoto University

8. Ken-ichi Inui PhD, Professor and Director, Department of Pharmacy, Kyoto University Hospital; Faculty of Medicine, Kyoto University

Abstract

OBJECTIVE To report a patient with a high tacrolimus blood concentration after lansoprazole administration and assess the potential interaction between tacrolimus and lansoprazole. CASE SUMMARY A 34-year-old Japanese man underwent a living-donor kidney transplantation having received tacrolimus, mycophenolate mofetil, and prednisolone for immunosuppression. Lansoprazole was administered from postoperative day 4 as prophylaxis of ulcers. The trough concentration of tacrolimus increased markedly after the introduction of lansoprazole, while results of liver function tests were within normal limits. Lansoprazole was stopped on day 15 and was replaced with famotidine on day 17. The trough concentration of tacrolimus returned to the therapeutic range after administration of lansoprazole ceased. Genetic analysis revealed a heterozygous mutation at exon 5 of the CYP2C19 gene (CYP2C19*1/*2) in this patient. DISCUSSION Lansoprazole is metabolized by 2 enzymes, CYP2C19 and CYP3A4. Since tacrolimus is also metabolized by CYP3A4, the blood concentration of tacrolimus in this patient who had a CYP2C19 gene mutation may have been elevated by decreased hepatic elimination of lansoprazole. An objective causality assessment revealed that this interaction was probable. CONCLUSIONS Trough concentrations of tacrolimus should be monitored closely for optimizing the dosage regimen in patients receiving concomitant lansoprazole.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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