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The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia
INTRODUCTION: Clozapine (CLZ) is the gold standard drug for treatment-refractory schizophrenia (TRS). However, approximately 30% of patients partially respond to CLZ, defining this subset with super refractory schizophrenia (SRS). Alterations in enzyme activity may affect CLZ responses; the CYP3A4,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023876/ https://www.ncbi.nlm.nih.gov/pubmed/32103962 http://dx.doi.org/10.2147/NDT.S228103 |
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author | Rodrigues-Silva, Christielly Semedo, Agostinho Tavares Neri, Hiasmin Franciely da Silva Vianello, Rosana Pereira Galaviz-Hernández, Carlos Sosa-Macías, Martha de Brito, Rodrigo Bernini Ghedini, Paulo César |
author_facet | Rodrigues-Silva, Christielly Semedo, Agostinho Tavares Neri, Hiasmin Franciely da Silva Vianello, Rosana Pereira Galaviz-Hernández, Carlos Sosa-Macías, Martha de Brito, Rodrigo Bernini Ghedini, Paulo César |
author_sort | Rodrigues-Silva, Christielly |
collection | PubMed |
description | INTRODUCTION: Clozapine (CLZ) is the gold standard drug for treatment-refractory schizophrenia (TRS). However, approximately 30% of patients partially respond to CLZ, defining this subset with super refractory schizophrenia (SRS). Alterations in enzyme activity may affect CLZ responses; the CYP3A4, CYP1A2 and CYP2C19 genes are primarily responsible for CLZ metabolism. OBJECTIVE: The aim of this study was to assess if CYP2C19 variants were associated with TRS or SRS. METHODS: CYP2C19*2 loss-of-function and CYP2C19*17 gain-of-function polymorphism genotype testing were performed in 108 individuals undergoing pharmacological treatment for TRS or SRS. DNA was extracted and polymorphisms were analyzed by polymerase chain reaction (PCR) and sequencing. RESULTS: CYP2C19*17 had positive correlations with SRS and lower Brief Psychiatric Rating Scale (BPRS) scores for TRS. In addition, CYP2C19*2 was associated with lower CLZ dosages for TRS. CONCLUSION: These results show that CYP2C19*2 and CYP2C19*17 polymorphisms influence CLZ responses during schizophrenia treatment. |
format | Online Article Text |
id | pubmed-7023876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-70238762020-02-26 The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia Rodrigues-Silva, Christielly Semedo, Agostinho Tavares Neri, Hiasmin Franciely da Silva Vianello, Rosana Pereira Galaviz-Hernández, Carlos Sosa-Macías, Martha de Brito, Rodrigo Bernini Ghedini, Paulo César Neuropsychiatr Dis Treat Original Research INTRODUCTION: Clozapine (CLZ) is the gold standard drug for treatment-refractory schizophrenia (TRS). However, approximately 30% of patients partially respond to CLZ, defining this subset with super refractory schizophrenia (SRS). Alterations in enzyme activity may affect CLZ responses; the CYP3A4, CYP1A2 and CYP2C19 genes are primarily responsible for CLZ metabolism. OBJECTIVE: The aim of this study was to assess if CYP2C19 variants were associated with TRS or SRS. METHODS: CYP2C19*2 loss-of-function and CYP2C19*17 gain-of-function polymorphism genotype testing were performed in 108 individuals undergoing pharmacological treatment for TRS or SRS. DNA was extracted and polymorphisms were analyzed by polymerase chain reaction (PCR) and sequencing. RESULTS: CYP2C19*17 had positive correlations with SRS and lower Brief Psychiatric Rating Scale (BPRS) scores for TRS. In addition, CYP2C19*2 was associated with lower CLZ dosages for TRS. CONCLUSION: These results show that CYP2C19*2 and CYP2C19*17 polymorphisms influence CLZ responses during schizophrenia treatment. Dove 2020-02-11 /pmc/articles/PMC7023876/ /pubmed/32103962 http://dx.doi.org/10.2147/NDT.S228103 Text en © 2020 Rodrigues-Silva et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Rodrigues-Silva, Christielly Semedo, Agostinho Tavares Neri, Hiasmin Franciely da Silva Vianello, Rosana Pereira Galaviz-Hernández, Carlos Sosa-Macías, Martha de Brito, Rodrigo Bernini Ghedini, Paulo César The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title | The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title_full | The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title_fullStr | The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title_full_unstemmed | The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title_short | The CYP2C19*2 and CYP2C19*17 Polymorphisms Influence Responses to Clozapine for the Treatment of Schizophrenia |
title_sort | cyp2c19*2 and cyp2c19*17 polymorphisms influence responses to clozapine for the treatment of schizophrenia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7023876/ https://www.ncbi.nlm.nih.gov/pubmed/32103962 http://dx.doi.org/10.2147/NDT.S228103 |
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