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Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia
OBJECTIVE: Olanzapine is an atypical antipsychotic drug commonly used for the treatment of schizophrenia. However, there are still many complications associated with the use of olanzapine, and researchers continually strive to improve the handling of data from regular therapeutic drug monitoring (TD...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104801/ https://www.ncbi.nlm.nih.gov/pubmed/30121590 http://dx.doi.org/10.1136/bmjopen-2017-020070 |
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author | Li, Anning Ji, Shuangmin Yue, Weihua Yan, Hao Dong, Fang Ruan, Canjun Li, Wenbiao Lu, Wei Zhang, Dai Wang, Chuanyue |
author_facet | Li, Anning Ji, Shuangmin Yue, Weihua Yan, Hao Dong, Fang Ruan, Canjun Li, Wenbiao Lu, Wei Zhang, Dai Wang, Chuanyue |
author_sort | Li, Anning |
collection | PubMed |
description | OBJECTIVE: Olanzapine is an atypical antipsychotic drug commonly used for the treatment of schizophrenia. However, there are still many complications associated with the use of olanzapine, and researchers continually strive to improve the handling of data from regular therapeutic drug monitoring (TDM). The objective of this study is to optimise the individualised treatment of olanzapine by establishing a population pharmacokinetics (PopPK) model in Chinese patients with schizophrenia. METHODS: This study integrates an extensive collection of concentration data from healthy volunteers after a single dose and a less extensive collection of samples from patients undergoing TDM. A PopPK model was developed using non-linear mixed-effects modelling. Potential covariates, including the olanzapine manufacturer and patient gender and age, were assessed during model development. A total of 616 plasma concentration levels from 22 healthy male individuals in China and 458 concentration levels from 112 male and 122 female patients with schizophrenia undergoing TDM at 12 hospitals in China were included in the analysis. The concentration profile could be best described using a two-compartment model with first-order absorption and elimination. RESULTS: The absorption rate (Ka) of olanzapine ranged from 2.85 h(–1) to 5.39 h(–1) for the different formulations. The typical absorption time delay was 0.877 hour. Body weight had a considerable effect on the apparent volume of the centre compartment and showed a power relationship. CONCLUSIONS: A PopPK model of olanzapine in Chinese patients with schizophrenia was developed in this study. After determining the PK parameters of olanzapine, the results suggested that body weight exhibited a considerable impact effect on V(C)/F. The impact of subjects and formulations requires further study. The PopPK model established in this study is likely to provide some information for the individualised therapy of olanzapine. TRIAL REGISTRATION NUMBER: ChiCTR-TRC-10000934; Results. |
format | Online Article Text |
id | pubmed-6104801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-61048012018-08-24 Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia Li, Anning Ji, Shuangmin Yue, Weihua Yan, Hao Dong, Fang Ruan, Canjun Li, Wenbiao Lu, Wei Zhang, Dai Wang, Chuanyue BMJ Open Mental Health OBJECTIVE: Olanzapine is an atypical antipsychotic drug commonly used for the treatment of schizophrenia. However, there are still many complications associated with the use of olanzapine, and researchers continually strive to improve the handling of data from regular therapeutic drug monitoring (TDM). The objective of this study is to optimise the individualised treatment of olanzapine by establishing a population pharmacokinetics (PopPK) model in Chinese patients with schizophrenia. METHODS: This study integrates an extensive collection of concentration data from healthy volunteers after a single dose and a less extensive collection of samples from patients undergoing TDM. A PopPK model was developed using non-linear mixed-effects modelling. Potential covariates, including the olanzapine manufacturer and patient gender and age, were assessed during model development. A total of 616 plasma concentration levels from 22 healthy male individuals in China and 458 concentration levels from 112 male and 122 female patients with schizophrenia undergoing TDM at 12 hospitals in China were included in the analysis. The concentration profile could be best described using a two-compartment model with first-order absorption and elimination. RESULTS: The absorption rate (Ka) of olanzapine ranged from 2.85 h(–1) to 5.39 h(–1) for the different formulations. The typical absorption time delay was 0.877 hour. Body weight had a considerable effect on the apparent volume of the centre compartment and showed a power relationship. CONCLUSIONS: A PopPK model of olanzapine in Chinese patients with schizophrenia was developed in this study. After determining the PK parameters of olanzapine, the results suggested that body weight exhibited a considerable impact effect on V(C)/F. The impact of subjects and formulations requires further study. The PopPK model established in this study is likely to provide some information for the individualised therapy of olanzapine. TRIAL REGISTRATION NUMBER: ChiCTR-TRC-10000934; Results. BMJ Publishing Group 2018-08-17 /pmc/articles/PMC6104801/ /pubmed/30121590 http://dx.doi.org/10.1136/bmjopen-2017-020070 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Mental Health Li, Anning Ji, Shuangmin Yue, Weihua Yan, Hao Dong, Fang Ruan, Canjun Li, Wenbiao Lu, Wei Zhang, Dai Wang, Chuanyue Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title | Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title_full | Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title_fullStr | Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title_full_unstemmed | Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title_short | Development of a population pharmacokinetic model of olanzapine for Chinese health volunteers and patients with schizophrenia |
title_sort | development of a population pharmacokinetic model of olanzapine for chinese health volunteers and patients with schizophrenia |
topic | Mental Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104801/ https://www.ncbi.nlm.nih.gov/pubmed/30121590 http://dx.doi.org/10.1136/bmjopen-2017-020070 |
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