Suzuki Yoshiharu, Yoshihashi Takuya, Takahashi Kazuhiro, Furuya Kinji, Ohkohchi Nobuhiro, Oda Tatsuya, Homma Masato
Department of Pharmacy, University of Tsukuba Hospital, Ibaraki 305-8576, Japan.
Department of Gastroenterological and Hepato-Biliary-Pancreatic Surgery, and Organ Transplantation, Faculty of Medicine, University of Tsukuba, Ibaraki 305-8575, Japan.
J Clin Med. 2021 Aug 31;10(17):3964. doi: 10.3390/jcm10173964.
Kidney transplant recipients with tacrolimus-based immunosuppressive therapy are often treated with proton-pump inhibitors (PPIs) to prevent gastric ulcer complications. Vonoprazan, a potassium-competitive acid blocker, is a novel PPI possessing different metabolic pathways from conventional PPIs (e.g., omeprazole, lansoprazole and rabeprazole). However, no data are available on the change in blood concentration of tacrolimus after switching rabeprazole, a conventional PPI, to vonoprazan coadministration in the initial period of post-transplantation. This is a retrospective study of 18 kidney transplant recipients. The blood concentration and the concentration to dose (C/D) ratio of tacrolimus were compared before and after switching from rabeprazole to vonoprazan. Impacts of and genetic polymorphisms on the drug-drug interaction were also examined. The median (range) trough concentration of tacrolimus was significantly increased from 5.2 (3.6-7.4) to 8.1 (6.1-11.7) ng/mL ( < 0.0005) after switching from rabeprazole to vonoprazan. The C/D ratio of tacrolimus was also significantly increased from 38.1 (16.5-138.1) to 48.9 (26.2-207.2) ( < 0.0005). The percent changes of tacrolimus concentrations and C/D were 65.8% and 41.8%, respectively. and genetic polymorphisms did not affect the change in concentration and C/D ratio of tacrolimus. The present study indicates that vonoprazan coadministration increases the tacrolimus concentration regardless of or genetic polymorphisms. Thus, frequent monitoring of blood tacrolimus concentration is required when vonoprazan is introduced as an intensive gastric acid blocker in the early phase of post-transplantation.
接受基于他克莫司的免疫抑制治疗的肾移植受者通常会使用质子泵抑制剂(PPI)来预防胃溃疡并发症。沃克奥美拉唑,一种钾离子竞争性酸阻滞剂,是一种新型PPI,其代谢途径与传统PPI(如奥美拉唑、兰索拉唑和雷贝拉唑)不同。然而,在移植后初期,将传统PPI雷贝拉唑换成沃克奥美拉唑联合用药后,他克莫司血药浓度的变化尚无相关数据。这是一项针对18名肾移植受者的回顾性研究。比较了从雷贝拉唑换成沃克奥美拉唑前后他克莫司的血药浓度及血药浓度与剂量(C/D)比。还研究了CYP2C19和CYP3A5基因多态性对药物相互作用的影响。从雷贝拉唑换成沃克奥美拉唑后,他克莫司的中位(范围)谷浓度从5.2(3.6 - 7.4)显著升至8.1(6.1 - 11.7)ng/mL(P < 0.0005)。他克莫司的C/D比也从38.1(16.5 - 138.1)显著升至48.9(26.2 - 207.2)(P < 0.0005)。他克莫司浓度和C/D的百分比变化分别为65.8%和41.8%。CYP2C19和CYP3A5基因多态性并未影响他克莫司浓度及C/D比变化。本研究表明,无论CYP2C19或CYP3A5基因多态性如何,沃克奥美拉唑联合用药都会增加他克莫司浓度。因此,在移植后早期将沃克奥美拉唑作为强效胃酸阻滞剂引入时,需要频繁监测他克莫司血药浓度。