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Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age

Objective: 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. Methods: Demo...

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Autores principales: Liu, Shujing, Xiao, Tao, Huang, Shanqing, Li, Xiaolin, Kong, Wan, Yang, Ye, Zhang, Zi, Ni, Xiaojia, Lu, Haoyang, Zhang, Ming, Shang, Dewei, Wen, Yuguan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340256/
https://www.ncbi.nlm.nih.gov/pubmed/35924062
http://dx.doi.org/10.3389/fphar.2022.964758
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author Liu, Shujing
Xiao, Tao
Huang, Shanqing
Li, Xiaolin
Kong, Wan
Yang, Ye
Zhang, Zi
Ni, Xiaojia
Lu, Haoyang
Zhang, Ming
Shang, Dewei
Wen, Yuguan
author_facet Liu, Shujing
Xiao, Tao
Huang, Shanqing
Li, Xiaolin
Kong, Wan
Yang, Ye
Zhang, Zi
Ni, Xiaojia
Lu, Haoyang
Zhang, Ming
Shang, Dewei
Wen, Yuguan
author_sort Liu, Shujing
collection PubMed
description Objective: 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. Methods: 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. Results: 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. Conclusion: 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.
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spelling pubmed-93402562022-08-02 Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age Liu, Shujing Xiao, Tao Huang, Shanqing Li, Xiaolin Kong, Wan Yang, Ye Zhang, Zi Ni, Xiaojia Lu, Haoyang Zhang, Ming Shang, Dewei Wen, Yuguan Front Pharmacol Pharmacology Objective: 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. Methods: 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. Results: 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. Conclusion: 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. Frontiers Media S.A. 2022-07-18 /pmc/articles/PMC9340256/ /pubmed/35924062 http://dx.doi.org/10.3389/fphar.2022.964758 Text en Copyright © 2022 Liu, Xiao, Huang, Li, Kong, Yang, Zhang, Ni, Lu, Zhang, Shang and Wen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Liu, Shujing
Xiao, Tao
Huang, Shanqing
Li, Xiaolin
Kong, Wan
Yang, Ye
Zhang, Zi
Ni, Xiaojia
Lu, Haoyang
Zhang, Ming
Shang, Dewei
Wen, Yuguan
Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title_full Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title_fullStr Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title_full_unstemmed Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title_short Population pharmacokinetics model for escitalopram in Chinese psychiatric patients: effect of CYP2C19 and age
title_sort population pharmacokinetics model for escitalopram in chinese psychiatric patients: effect of cyp2c19 and age
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9340256/
https://www.ncbi.nlm.nih.gov/pubmed/35924062
http://dx.doi.org/10.3389/fphar.2022.964758
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