Pharmacokinetic Evaluation of Tacrolimus in Chinese Adult Patients during the Early Stages Post-Lung Transplantation

• Published in: Journal of personalized medicine Vol. 13; no. 4; p. 656
• Main Authors: Cui, Yi-Fan, Pan, Yan, Zhu, Min-Fang, Jiao, Zheng
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 11.04.2023; MDPI
• Subjects: Analysis; Cystic fibrosis; Drug dosages; Enzymes; Ethylenediaminetetraacetic acid; Gene polymorphism; Genetic polymorphisms; Immunotherapy; Lung transplantation; Lung transplants; Mycophenolate mofetil; Patients; Pharmacokinetics; Population; Precision medicine; Steroids; Surgery; Tacrolimus; Transplantation of organs, tissues, etc; White people; China; Belgium; United States > US; Ireland; Chinese population; pharmacokinetics; lung transplantation; tacrolimus; CYP3A4/5 enzyme
• ISSN: 2075-4426; 2075-4426
• DOI: 10.3390/jpm13040656

Although tacrolimus has been widely used in patients undergoing lung transplantation, few studies have reported the pharmacokinetics of tacrolimus in Chinese patients after lung transplantation. Thus, we aimed to investigate the pharmacokinetics and influential factors in this patient cohort in the early stage after lung transplantation. We enrolled 14 adult lung transplant recipients who were treated with tacrolimus and then intensively collected blood samples within a 12-h dosing interval. The pharmacokinetic parameters of tacrolimus were calculated using non-compartmental analysis, and the influence of pathophysiological characteristics and CYP3A5*3 and CYP3A4*1G genotypes on the pharmacokinetics of tacrolimus was assessed. Using linear regression analysis, we investigated the correlation between tacrolimus concentration at different sampling points and measured the area under the time-concentration curve (AUC ). Geometric mean of apparent clearance (CL/F) was 18.13 ± 1.65 L/h in non-CYP3A5*3/*3 carriers, five times higher than that in CYP3A5*3/*3 carriers ( < 0.001). Furthermore, the tacrolimus concentration 4 h after administration had the strongest correlation with AUC (R = 0.979). The pharmacokinetics of tacrolimus varied largely between patients during the early stage post-transplantation, which could be partially explained by CYP3A5*3 genetic polymorphisms.