Population pharmacokinetics analysis of olanzapine for Chinese psychotic patients based on clinical therapeutic drug monitoring data with assistance of meta-analysis

被引:16
|
作者
Yin, Anyue [1 ,2 ,3 ]
Shang, Dewei [4 ]
Wen, Yuguan [4 ]
Li, Liang [1 ,2 ,3 ]
Zhou, Tianyan [1 ,2 ,3 ]
Lu, Wei [1 ,2 ,3 ,5 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Beijing 100191, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Pfizer Pharmacometr Educ Ctr, Beijing 100191, Peoples R China
[3] Peking Univ, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China
[4] Guangzhou Med Univ, Affiliated Brain Hosp, Guangzhou Huiai Hosp, Guangzhou Brain Hosp, Guangzhou 510370, Guangdong, Peoples R China
[5] Beijing Inst Brain Disorders, Beijing 100088, Peoples R China
基金
中国国家自然科学基金;
关键词
Olanzapine; Psychotic; Population pharmacokinetic model; Model-based meta-analysis; Therapeutic drug monitoring; HEALTHY-VOLUNTEERS; ANTIPSYCHOTIC-DRUGS; SCHIZOPHRENIA; MODEL; BIOEQUIVALENCE; DISPOSITION; TABLET; FORMULATIONS; FLUVOXAMINE; CLOZAPINE;
D O I
10.1007/s00228-016-2040-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study was to build an eligible population pharmacokinetic (PK) model for olanzapine in Chinese psychotic patients based on therapeutic drug monitoring (TDM) data, with assistance of meta-analysis, to facilitate individualized therapy. Population PK analysis for olanzapine was performed using NONMEM software (version 7.3.0). TDM data were collected from Guangzhou Brain Hospital (China). Because of the limitations of TDM data, model-based meta-analysis was performed to construct a structural model to assist the modeling of TDM data as prior estimates. After analyzing related covariates, a simulation was performed to predict concentrations for different types of patients under common dose regimens. A two-compartment model with first-order absorption and elimination was developed for olanzapine oral tablets, based on 23 articles with 390 data points. The model was then applied to the TDM data. Gender and smoking habits were found to be significant covariates that influence the clearance of olanzapine. To achieve a blood concentration of 20 ng/mL (the lower boundary of the recommended therapeutic range), simulation results indicated that the dose regimen of olanzapine should be 5 mg BID (twice a day), a parts per thousand yen 5 mg QD (every day) plus 10 mg QN (every night), or > 10 mg BID for female nonsmokers, male nonsmokers and male smokers, respectively. The population PK model, built using meta-analysis, could facilitate the modeling of TDM data collected from Chinese psychotic patients. The factors that significantly influence olanzapine disposition were determined and the final model could be used for individualized treatment.
引用
收藏
页码:933 / 944
页数:12
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