Liu Shujing, Xiao Tao, Huang Shanqing, Li Xiaolin, Kong Wan, Yang Ye, Zhang Zi, Ni Xiaojia, Lu Haoyang, Zhang Ming, Shang Dewei, Wen Yuguan
Department of Pharmacy, The Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
Guangdong Engineering Technology Research Center for Translational Medicine of Mental Disorders, Guangzhou, China.
Front Pharmacol. 2022 Jul 18;13:964758. doi: 10.3389/fphar.2022.964758. eCollection 2022.
To establish a population pharmacokinetic model in Chinese psychiatric patients to characterize escitalopram pharmacokinetic profile to identify factors influencing drug exposure, and through simulation to compare the results with the established therapeutic reference range. Demographic information, dosing regimen, CYP2C19 genotype, concomitant medications, and liver and kidney function indicators were retrospectively collected for inpatients taking escitalopram with therapeutic drug monitoring from 2018 to 2021. Nonlinear mixed-effects modeling was used to model the pharmacokinetic characteristics of escitalopram. Goodness-of-fit plots, bootstrapping, and normalized prediction distribution errors were used to evaluate the model. Simulation for different dosing regimens was based on the final estimations. The study comprised 106 patients and 337 measurements of serum sample. A structural model with one compartment with first-order absorption and elimination described the data adequately. The population-estimated apparent volume of distribution and apparent clearance were 815 and 16.3 L/h, respectively. Age and CYP2C19 phenotype had a significant effect on the apparent clearance (CL/F). CL/F of escitalopram decreased with increased age, and CL/F of poor metabolizer patients was significantly lower than in extensive and immediate metabolizer patients. The final model-based simulation showed that the daily dose of adolescents with poor metabolizer might be as high as 15 mg or 20 mg and referring to the therapeutic range for adults may result in overdose and a high risk of adverse effects in older patients. A population pharmacokinetics model of escitalopram was successfully created for the Chinese population. Depending on the age of the patients, CYP2C19 genotype and serum drug concentrations throughout treatment are required for adequate individualization of dosing regimens. When developing a regimen for older patients, especially those who are poor metabolizers, vigilance is required.
建立中国精神科患者的群体药代动力学模型,以表征艾司西酞普兰的药代动力学特征,识别影响药物暴露的因素,并通过模拟将结果与既定的治疗参考范围进行比较。回顾性收集了2018年至2021年接受艾司西酞普兰治疗并进行治疗药物监测的住院患者的人口统计学信息、给药方案、CYP2C19基因型、合并用药以及肝肾功能指标。采用非线性混合效应模型对艾司西酞普兰的药代动力学特征进行建模。使用拟合优度图、自抽样法和标准化预测分布误差来评估模型。基于最终估计值对不同给药方案进行模拟。该研究包括106例患者和337次血清样本测量。一个具有一级吸收和消除的单室结构模型能够充分描述数据。群体估计的表观分布容积和表观清除率分别为815L和16.3L/h。年龄和CYP2C19表型对表观清除率(CL/F)有显著影响。艾司西酞普兰的CL/F随年龄增长而降低,慢代谢患者的CL/F显著低于快代谢和超快速代谢患者。基于最终模型的模拟显示,慢代谢青少年的日剂量可能高达15mg或20mg,参考成人治疗范围可能导致老年患者用药过量和不良反应风险增加。成功建立了中国人群的艾司西酞普兰群体药代动力学模型。根据患者年龄、CYP2C19基因型以及整个治疗过程中的血清药物浓度,对给药方案进行充分个体化调整是必要的。在为老年患者,尤其是慢代谢患者制定治疗方案时,需要谨慎。