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Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?

Schizophrenia (SCZ) is a complex psychiatric disorder of multifactorial origin, in which both genetic and environmental factors have an impact on its onset, course, and outcome. Large variability in response and tolerability of medication among individuals makes it difficult to predict the efficacy...

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Autores principales: Płaza, Olga, Gałecki, Piotr, Orzechowska, Agata, Gałecka, Małgorzata, Sobolewska-Nowak, Justyna, Szulc, Agata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775397/
https://www.ncbi.nlm.nih.gov/pubmed/36551925
http://dx.doi.org/10.3390/biomedicines10123165
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author Płaza, Olga
Gałecki, Piotr
Orzechowska, Agata
Gałecka, Małgorzata
Sobolewska-Nowak, Justyna
Szulc, Agata
author_facet Płaza, Olga
Gałecki, Piotr
Orzechowska, Agata
Gałecka, Małgorzata
Sobolewska-Nowak, Justyna
Szulc, Agata
author_sort Płaza, Olga
collection PubMed
description Schizophrenia (SCZ) is a complex psychiatric disorder of multifactorial origin, in which both genetic and environmental factors have an impact on its onset, course, and outcome. Large variability in response and tolerability of medication among individuals makes it difficult to predict the efficacy of a chosen therapeutic method and create universal and precise guidelines for treatment. Pharmacogenetic research allows for the identification of genetic polymorphisms associated with response to a chosen antipsychotic, thus allowing for a more effective and personal approach to treatment. This review focuses on three frequently prescribed second-generation antipsychotics (SGAs), risperidone, olanzapine, and aripiprazole, and aims to analyze the current state and future perspectives in research dedicated to identifying genetic factors associated with antipsychotic response. Multiple alleles of genes involved in pharmacokinetics (particularly isoenzymes of cytochrome P450), as well as variants of genes involved in dopamine, serotonin, and glutamate neurotransmission, have already been identified as ones of significant impact on antipsychotic response. It must, however, be noted that although currently obtained results are promising, trials with bigger study groups and unified protocols are crucial for standardizing methods and determining objective antipsychotic response status.
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spelling pubmed-97753972022-12-23 Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics? Płaza, Olga Gałecki, Piotr Orzechowska, Agata Gałecka, Małgorzata Sobolewska-Nowak, Justyna Szulc, Agata Biomedicines Review Schizophrenia (SCZ) is a complex psychiatric disorder of multifactorial origin, in which both genetic and environmental factors have an impact on its onset, course, and outcome. Large variability in response and tolerability of medication among individuals makes it difficult to predict the efficacy of a chosen therapeutic method and create universal and precise guidelines for treatment. Pharmacogenetic research allows for the identification of genetic polymorphisms associated with response to a chosen antipsychotic, thus allowing for a more effective and personal approach to treatment. This review focuses on three frequently prescribed second-generation antipsychotics (SGAs), risperidone, olanzapine, and aripiprazole, and aims to analyze the current state and future perspectives in research dedicated to identifying genetic factors associated with antipsychotic response. Multiple alleles of genes involved in pharmacokinetics (particularly isoenzymes of cytochrome P450), as well as variants of genes involved in dopamine, serotonin, and glutamate neurotransmission, have already been identified as ones of significant impact on antipsychotic response. It must, however, be noted that although currently obtained results are promising, trials with bigger study groups and unified protocols are crucial for standardizing methods and determining objective antipsychotic response status. MDPI 2022-12-07 /pmc/articles/PMC9775397/ /pubmed/36551925 http://dx.doi.org/10.3390/biomedicines10123165 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Płaza, Olga
Gałecki, Piotr
Orzechowska, Agata
Gałecka, Małgorzata
Sobolewska-Nowak, Justyna
Szulc, Agata
Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title_full Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title_fullStr Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title_full_unstemmed Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title_short Pharmacogenetics and Schizophrenia—Can Genomics Improve the Treatment with Second-Generation Antipsychotics?
title_sort pharmacogenetics and schizophrenia—can genomics improve the treatment with second-generation antipsychotics?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9775397/
https://www.ncbi.nlm.nih.gov/pubmed/36551925
http://dx.doi.org/10.3390/biomedicines10123165
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