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CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population
Depression disorder is one of the most serious mental illnesses in the world. Escitalopram is the essential first-line medication for depression disorder. It is the substrate of hepatic cytochrome P450 (CYP) enzyme CYP2C19 with high polymorphism. The effect of CYP2C19 on pharmacokinetics and pharmac...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429954/ https://www.ncbi.nlm.nih.gov/pubmed/34512354 http://dx.doi.org/10.3389/fphar.2021.730461 |
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author | Huang, Xinyi Li, Chao Li, Chaopeng Li, Zhenyu Li, Xiaohui Liao, Jianwei Rao, Tai Chen, Lulu Gao, Lichen Ouyang, Dongsheng |
author_facet | Huang, Xinyi Li, Chao Li, Chaopeng Li, Zhenyu Li, Xiaohui Liao, Jianwei Rao, Tai Chen, Lulu Gao, Lichen Ouyang, Dongsheng |
author_sort | Huang, Xinyi |
collection | PubMed |
description | Depression disorder is one of the most serious mental illnesses in the world. Escitalopram is the essential first-line medication for depression disorder. It is the substrate of hepatic cytochrome P450 (CYP) enzyme CYP2C19 with high polymorphism. The effect of CYP2C19 on pharmacokinetics and pharmacodynamics on Caucasian population has been studied. The Clinical Pharmacogenetics Implementation Consortium Guideline provides dosing recommendations for escitalopram on CYP2C19 genotypes on the basis of the studies on Caucasian population. However, the gene frequency of the alleles of CYP2C19 showed racial differences between Chinese and Caucasian populations. Representatively, the frequency of the *2 and *3 allele, which were considered as poor metabolizer, has been shown to be three times higher in Chinese than in Caucasians. In addition, the environments might also lead to different degrees of impacts on genotypes. Therefore, the guidelines based on the Caucasians may not be applicable to the Chinese, which induced the establishment of a guideline in China. It is necessary to provide the evidence of individual treatment of escitalopram in Chinese by studying the effect of CYP2C19 genotypes on the pharmacokinetics parameters and steady-state concentration on Chinese. In this study, single-center, randomized, open-label, two-period, two-treatment crossover studies were performed. Ninety healthy Chinese subjects finished the trials, and they were included in the statistical analysis. The pharmacokinetics characteristics of different genotypes in Chinese were obtained. The results indicate that the poor metabolizer had higher exposure, and increased half-life than the extensive metabolizer and intermediate metabolite. The prediction of steady-state concentration based on the single dose trial on escitalopram shows that the poor metabolizer might have a higher steady-state concentration than the extensive metabolizer and intermediate metabolite in Chinese. The results indicate that the genetic testing before medication and the adjustment of escitalopram in the poor metabolizer should be considered in the clinical treatments in Chinese. The results provide the evidence of individual treatment of escitalopram in Chinese, which will be beneficial for the safer and more effective application of escitalopram in the Chinese population. Clinical Trial Registration: identifier ChiCTR1900027226. |
format | Online Article Text |
id | pubmed-8429954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84299542021-09-11 CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population Huang, Xinyi Li, Chao Li, Chaopeng Li, Zhenyu Li, Xiaohui Liao, Jianwei Rao, Tai Chen, Lulu Gao, Lichen Ouyang, Dongsheng Front Pharmacol Pharmacology Depression disorder is one of the most serious mental illnesses in the world. Escitalopram is the essential first-line medication for depression disorder. It is the substrate of hepatic cytochrome P450 (CYP) enzyme CYP2C19 with high polymorphism. The effect of CYP2C19 on pharmacokinetics and pharmacodynamics on Caucasian population has been studied. The Clinical Pharmacogenetics Implementation Consortium Guideline provides dosing recommendations for escitalopram on CYP2C19 genotypes on the basis of the studies on Caucasian population. However, the gene frequency of the alleles of CYP2C19 showed racial differences between Chinese and Caucasian populations. Representatively, the frequency of the *2 and *3 allele, which were considered as poor metabolizer, has been shown to be three times higher in Chinese than in Caucasians. In addition, the environments might also lead to different degrees of impacts on genotypes. Therefore, the guidelines based on the Caucasians may not be applicable to the Chinese, which induced the establishment of a guideline in China. It is necessary to provide the evidence of individual treatment of escitalopram in Chinese by studying the effect of CYP2C19 genotypes on the pharmacokinetics parameters and steady-state concentration on Chinese. In this study, single-center, randomized, open-label, two-period, two-treatment crossover studies were performed. Ninety healthy Chinese subjects finished the trials, and they were included in the statistical analysis. The pharmacokinetics characteristics of different genotypes in Chinese were obtained. The results indicate that the poor metabolizer had higher exposure, and increased half-life than the extensive metabolizer and intermediate metabolite. The prediction of steady-state concentration based on the single dose trial on escitalopram shows that the poor metabolizer might have a higher steady-state concentration than the extensive metabolizer and intermediate metabolite in Chinese. The results indicate that the genetic testing before medication and the adjustment of escitalopram in the poor metabolizer should be considered in the clinical treatments in Chinese. The results provide the evidence of individual treatment of escitalopram in Chinese, which will be beneficial for the safer and more effective application of escitalopram in the Chinese population. Clinical Trial Registration: identifier ChiCTR1900027226. Frontiers Media S.A. 2021-08-27 /pmc/articles/PMC8429954/ /pubmed/34512354 http://dx.doi.org/10.3389/fphar.2021.730461 Text en Copyright © 2021 Huang, Li, Li, Li, Li, Liao, Rao, Chen, Gao and Ouyang. 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 Huang, Xinyi Li, Chao Li, Chaopeng Li, Zhenyu Li, Xiaohui Liao, Jianwei Rao, Tai Chen, Lulu Gao, Lichen Ouyang, Dongsheng CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title | CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title_full | CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title_fullStr | CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title_full_unstemmed | CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title_short | CYP2C19 Genotyping May Provide a Better Treatment Strategy when Administering Escitalopram in Chinese Population |
title_sort | cyp2c19 genotyping may provide a better treatment strategy when administering escitalopram in chinese population |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8429954/ https://www.ncbi.nlm.nih.gov/pubmed/34512354 http://dx.doi.org/10.3389/fphar.2021.730461 |
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