Population pharmacokinetics model and initial dose optimization of tacrolimus in children and adolescents with lupus nephritis based on real-world data

被引:13
作者
Chen, Xiao [1 ]
Wang, Dong-Dong [1 ]
Xu, Hong [2 ]
Li, Zhi-Ping [1 ]
机构
[1] Fudan Univ, Childrens Hosp, Dept Pharm, 399 Wanyuan Rd, Shanghai 201102, Peoples R China
[2] Fudan Univ, Childrens Hosp, Dept Nephrol, 399 Wanyuan Rd, Shanghai 201102, Peoples R China
关键词
population pharmacokinetics; initial dose optimization; tacrolimus; children and adolescents; lupus nephritis; VERSUS-HOST-DISEASE; SCHISANDRA-SPHENANTHERA EXTRACT; JUVENILE IDIOPATHIC ARTHRITIS; RESISTANT NEPHROTIC SYNDROME; RENAL-TRANSPLANT RECIPIENTS; MARROW-TRANSPLANTATION; PEDIATRIC LUPUS; EARLY PERIOD; ONSET LUPUS; ERYTHEMATOSUS;
D O I
10.3892/etm.2020.8821
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The present study aimed to establish a population pharmacokinetics model of tacrolimus and further optimize the initial dosing regimen of tacrolimus in pediatric and adolescent patients with lupus nephritis (LN). Pediatric and adolescent patients with LN were recruited between August 2014 and September 2019 at the Children's Hospital of Fudan University (Shanghai, China). Relevant information was used to set up a population pharmacokinetics model with a Nonlinear Mixed Effect Model and the initial dosage regimen was simulated with the Monte Carlo method. Body weight and co-administration of wuzhi capsule were indicated to influence tacrolimus clearance in pediatric and adolescent patients with LN, and at the same body weight, the rate of tacrolimus clearance in patients without vs. with co-administration of wuzhi capsule was 1:0.71. In addition, in patients who were not administered wuzhi capsule, an initial dosage regimen of 0.15 mg/kg/day was recommended for a body weight of 10-23 kg and 0.10 mg/kg/day for 23-60 kg; in patients who were administered wuzhi capsule, an initial dosage regimen of 0.10 mg/kg/day was recommended for a body weight of 10-23 kg and 0.05 mg/kg/day for 23-60 kg. To the best of our knowledge, the present study was the first to establish a population pharmacokinetics model of tacrolimus in order to determine the optimal initial dosage regimen of tacrolimus in pediatric and adolescent patients with LN.
引用
收藏
页码:1423 / 1430
页数:8
相关论文
共 86 条
[81]   Population Pharmacokinetics and Pharmacogenetics of Tacrolimus in De Novo Pediatric Kidney Transplant Recipients [J].
Zhao, W. ;
Elie, V. ;
Roussey, G. ;
Brochard, K. ;
Niaudet, P. ;
Leroy, V. ;
Loirat, C. ;
Cochat, P. ;
Cloarec, S. ;
Andre, J. L. ;
Garaix, F. ;
Bensman, A. ;
Fakhoury, M. ;
Jacqz-Aigrain, E. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 86 (06) :609-618
[82]   Pharmacometrics: a quantitative tool of pharmacological research [J].
Zheng, Qing-shan ;
Li, Lu-jin .
ACTA PHARMACOLOGICA SINICA, 2012, 33 (11) :1337-1338
[83]   Population Pharmacokinetics and Dosing Optimization of Azithromycin in Children with Community-Acquired Pneumonia [J].
Zheng, Yi ;
Liu, Shu-Ping ;
Xu, Bao-Ping ;
Shi, Zhong-Ren ;
Wang, Kai ;
Yang, Jin-Bin ;
Huang, Xin ;
Tang, Bo-Hao ;
Chen, Xing-Kai ;
Shi, Hai-Yan ;
Zhou, Yue ;
Wu, Yue-E ;
Qi, Hui ;
Jacqz-Aigrain, Evelyne ;
Shen, A-Dong ;
Zhao, Wei .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2018, 62 (09)
[84]   Efficacy and safety of tacrolimus in induction therapy of patients with lupus nephritis [J].
Zhou, Tianbiao ;
Lin, Shujun ;
Yang, Shen ;
Lin, Wenshan .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2019, 13 :857-869
[85]   Effects of CYP3A5 genotypes, ABCB1 C3435T and G2677T/A polymorphism on pharmacokinetics of Tacrolimus in Chinese adult liver transplant patients (Publication with Expression of Concern. See vol. 50, pg. 1265, 2020) [J].
Zhu, LiQin ;
Yang, JianWei ;
Zhang, Yuan ;
Jing, YaQing ;
Zhang, YanWen ;
Li, Guang .
XENOBIOTICA, 2015, 45 (09) :840-846
[86]   Effects of CYP3A4 and CYP3A5 polymorphisms on tacrolimus pharmacokinetics in Chinese adult renal transplant recipients: a population pharmacokinetic analysis [J].
Zuo, Xiao-cong ;
Ng, Chee M. ;
Barrett, Jeffrey S. ;
Luo, Ai-jing ;
Zhang, Bi-kui ;
Deng, Chen-hui ;
Xi, Lan-yan ;
Cheng, Ke ;
Ming, Ying-zi ;
Yang, Guo-ping ;
Pei, Qi ;
Zhu, Li-jun ;
Yuan, Hong ;
Liao, Hai-qiang ;
Ding, Jun-jie ;
Wu, Di ;
Zhou, Ya-nan ;
Jing, Ning-ning ;
Huang, Zhi-jun .
PHARMACOGENETICS AND GENOMICS, 2013, 23 (05) :251-261