Population pharmacokinetics and Bayesian estimation of mycophenolic acid concentrations in Chinese adult renal transplant recipients

被引:26
|
作者
Yu, Zi-cheng [1 ]
Zhou, Pei-jun [2 ]
Wang, Xiang-hui [2 ]
Francoise, Bressolle [3 ]
Xu, Da
Zhang, Wei-xia [4 ]
Chen, Bing [4 ]
机构
[1] Tongji Univ, Sch Med, Yangpu Hosp, Inst Clin Pharm & Pharmacol, Shanghai 200090, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Organ Transplantat Ctr, Shanghai 200025, Peoples R China
[3] Univ Montpellier I, Fac Pharm, Lab Pharmacocinet Clin, Montpellier, France
[4] Shanghai Jiao Tong Univ, Sch Med, Ruijin Hosp, Inst Clin Pharmacol, Shanghai 200025, Peoples R China
基金
中国国家自然科学基金;
关键词
renal transplantation; mycophenolate mofetil (MMF); mycophenolic acid (MPA); population pharmacokinetics; uridine diphosphate glucuronosyltransferase (UGT); LIMITED SAMPLING STRATEGY; UNDER-THE-CURVE; LOW-DOSE MYCOPHENOLATE; KIDNEY-TRANSPLANTATION; ALLOGRAFT RECIPIENTS; MOFETIL; POLYMORPHISMS; EXPOSURE; AREA; GLUCURONIDE;
D O I
10.1038/aps.2017.115
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mycophenolate mofetil (MMF) is an important immunosuppressant used in renal transplantation, and mycophenolic acid (MPA) is the active component released from the ester prodrug MMF. The objective of this study was to investigate the population pharmacokinetics of mycophenolic acid (MPA) following oral administration of MMF in Chinese adult renal transplant recipients and to identify factors that explain MPA pharmacokinetic variability. Pharmacokinetic data for MPA and covariate information were retrospectively collected from 118 patients (79 patients were assigned to the group for building the population pharmacokinetic model, while 39 patients were assigned to the validation group). Population pharmacokinetic data analysis was performed using the NONMEM software. The pharmacokinetics of MPA was best described by a two-compartment model with a first-order absorption rate with no lag time. Body weight and serum creatinine level were positively correlated with apparent clearance (CL/F). The polymorphism in uridine diphosphate glucuronosyltransferase gene, UGT2B7, significantly explained the interindividual variability in the initial volume of distribution (V-1/ F). The estimated population parameters (and interindividual variability) were CL/F 18.3 L/h (34.2%) and V-1/F 27.9 L (21.3%). The interoccasion variability was 13.7%. These population pharmacokinetic data have significant clinical value for the individualization of MMF therapy in Chinese adult renal transplant patients.
引用
收藏
页码:1566 / 1579
页数:14
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