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CYP3A5 Genotype-Dependent Drug-Drug Interaction Between Tacrolimus and Voriconazole in Chinese Kidney Transplant Patients

他克莫司 药品 伏立康唑 CYP3A5 医学 药理学 肾移植 基因型 肾移植 内科学 生物 移植 遗传学 基因 抗真菌 皮肤病科
作者
Yundi Zhang,Yue Du,Shuyu Ren,Yue Li,Xiaoming Zhang,Xiaohong Cao,Fengxi Liu,Huiying Zong,Yan Li
出处
期刊:Annals of Pharmacotherapy [SAGE]
卷期号:58 (6): 605-613 被引量:4
标识
DOI:10.1177/10600280231197399
摘要

Background: The effect of drug-drug interaction (DDI) between tacrolimus and voriconazole on the pharmacokinetics of tacrolimus in different CYP3A5 genotypes has not been reported in previous studies. Objective: The objective of this study was to investigate whether CYP3A5 genotype could influence tacrolimus-voriconazole DDI in Chinese kidney transplant patients. Methods: All kidney transplant patients were divided into combination and non-combination groups based on whether tacrolimus was combined with or without voriconazole. Each group was subdivided into CYP3A5 expresser ( CYP3A5*1/*1 or CYP3A5*1/*3) and CYP3A5 nonexpresser ( CYP3A5*3/*3). A retrospective analysis compared tacrolimus dose (D)-corrected trough concentrations (C 0 ) (C 0 /D) between combination and non-combination groups, respectively. Tacrolimus C 0 /D was also compared between CYP3A5 expresser and nonexpresser in both groups. Results: The C 0 /D values of tacrolimus were significantly different between CYP3A5 expresser and nonexpresser in combination group (378.20 [219.38, 633.48] ng/mL/[mg/kg/d] vs 720.00 [595.35, 1681.50] ng/mL/[mg/kg/d], P = 0.0010). Either in C YP3A5 expresser or nonexpresser, we found a statistically significant difference in tacrolimus C 0 /D between combination and non-combination group ( P < 0.0001). The increase in CYP3A5 nonexpresser was 1.38 times higher than that in CYP3A5 expresser (320.93% vs 232.19%). Conclusion and Relevance: The median C 0 /D values were 90.38% higher in kidney transplant recipients with CYP3A5*3/*3 genotype than in those with CYP3A5*1/*1 or CYP3A5*1/*3 genotype when treated with both tacrolimus and voriconazole. A CYP3A5 genotype-dependent DDI was found between tacrolimus and voriconazole. Therefore, personalized therapy accounting for CYP3A5 genotype detection and therapeutic drug monitoring is necessary for kidney transplant patients when treating with tacrolimus and voriconazole.
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