Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy

Detalhes bibliográficos
Autor(a) principal: Correia, Catarina
Data de Publicação: 2022
Outros Autores: Alcobia, Luciano, Lopes, Manuel J., Advinha, Ana M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/18229
Resumo: Objective: The main goal of this work was to identify, describe, characterize, and classify the scientifc evidence regarding the use of pharmacogenomic biomarkers in antidepressant treatment. Methods: The work was developed in two phases: i) a search for pharmacogenomic biomarkers in summaries of antidepressant drugs with marketing authorization in Portugal; and ii) a systematic literature review based on the data obtained in the frst phase, with the main objective of fnding international literature that could describe and characterize previously reported biomarkers and identify other relevant biomarkers. Finally, the levels of evidence and recommendation grades were classifed. Results: Among the 26 drugs with marketing authorization in Portugal, only 16 had pharmacogenomic information. The most widely studied pharmacogenomic biomarker was CYP2D6. These results were mostly supported by the systematic literature review, which yielded 103 papers, 63 of which were ultimately included in the review. The sys‑ tematic literature review also revealed the existence of other relevant biomarkers. Most of the included studies show a good level of evidence, which guarantees reliability and good recommendation grades. For the database (built during phase i), the results were informative but resulted in no specifc recommendations. Conclusions: Most pharmacogenomic variants are not studied or acknowledged by genetic tests, and more scien‑ tifc research is needed to confrm their usefulness. Therefore, only a small number of variants are considered when prescribing antidepressant drugs. In addition, genotyping of patients is not common in clinical practice.
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spelling Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapyAntidepressantsBiomarkersDepressionPharmacogenomicPharmacotherapyObjective: The main goal of this work was to identify, describe, characterize, and classify the scientifc evidence regarding the use of pharmacogenomic biomarkers in antidepressant treatment. Methods: The work was developed in two phases: i) a search for pharmacogenomic biomarkers in summaries of antidepressant drugs with marketing authorization in Portugal; and ii) a systematic literature review based on the data obtained in the frst phase, with the main objective of fnding international literature that could describe and characterize previously reported biomarkers and identify other relevant biomarkers. Finally, the levels of evidence and recommendation grades were classifed. Results: Among the 26 drugs with marketing authorization in Portugal, only 16 had pharmacogenomic information. The most widely studied pharmacogenomic biomarker was CYP2D6. These results were mostly supported by the systematic literature review, which yielded 103 papers, 63 of which were ultimately included in the review. The sys‑ tematic literature review also revealed the existence of other relevant biomarkers. Most of the included studies show a good level of evidence, which guarantees reliability and good recommendation grades. For the database (built during phase i), the results were informative but resulted in no specifc recommendations. Conclusions: Most pharmacogenomic variants are not studied or acknowledged by genetic tests, and more scien‑ tifc research is needed to confrm their usefulness. Therefore, only a small number of variants are considered when prescribing antidepressant drugs. In addition, genotyping of patients is not common in clinical practice.MDPISapientiaCorreia, CatarinaAlcobia, LucianoLopes, Manuel J.Advinha, Ana M.2022-09-08T09:17:52Z2022-08-302022-09-01T03:19:49Z2022-08-30T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/18229engBMC Psychiatry. 2022 Aug 30;22(1):57610.1186/s12888-022-04225-21471-244Xinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-24T10:30:26Zoai:sapientia.ualg.pt:10400.1/18229Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:07:59.060085Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
title Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
spellingShingle Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
Correia, Catarina
Antidepressants
Biomarkers
Depression
Pharmacogenomic
Pharmacotherapy
title_short Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
title_full Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
title_fullStr Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
title_full_unstemmed Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
title_sort Pharmacogenomic biomarkers as source of evidence of the effectiveness and safety of antidepressant therapy
author Correia, Catarina
author_facet Correia, Catarina
Alcobia, Luciano
Lopes, Manuel J.
Advinha, Ana M.
author_role author
author2 Alcobia, Luciano
Lopes, Manuel J.
Advinha, Ana M.
author2_role author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Correia, Catarina
Alcobia, Luciano
Lopes, Manuel J.
Advinha, Ana M.
dc.subject.por.fl_str_mv Antidepressants
Biomarkers
Depression
Pharmacogenomic
Pharmacotherapy
topic Antidepressants
Biomarkers
Depression
Pharmacogenomic
Pharmacotherapy
description Objective: The main goal of this work was to identify, describe, characterize, and classify the scientifc evidence regarding the use of pharmacogenomic biomarkers in antidepressant treatment. Methods: The work was developed in two phases: i) a search for pharmacogenomic biomarkers in summaries of antidepressant drugs with marketing authorization in Portugal; and ii) a systematic literature review based on the data obtained in the frst phase, with the main objective of fnding international literature that could describe and characterize previously reported biomarkers and identify other relevant biomarkers. Finally, the levels of evidence and recommendation grades were classifed. Results: Among the 26 drugs with marketing authorization in Portugal, only 16 had pharmacogenomic information. The most widely studied pharmacogenomic biomarker was CYP2D6. These results were mostly supported by the systematic literature review, which yielded 103 papers, 63 of which were ultimately included in the review. The sys‑ tematic literature review also revealed the existence of other relevant biomarkers. Most of the included studies show a good level of evidence, which guarantees reliability and good recommendation grades. For the database (built during phase i), the results were informative but resulted in no specifc recommendations. Conclusions: Most pharmacogenomic variants are not studied or acknowledged by genetic tests, and more scien‑ tifc research is needed to confrm their usefulness. Therefore, only a small number of variants are considered when prescribing antidepressant drugs. In addition, genotyping of patients is not common in clinical practice.
publishDate 2022
dc.date.none.fl_str_mv 2022-09-08T09:17:52Z
2022-08-30
2022-09-01T03:19:49Z
2022-08-30T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/18229
url http://hdl.handle.net/10400.1/18229
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv BMC Psychiatry. 2022 Aug 30;22(1):576
10.1186/s12888-022-04225-2
1471-244X
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv MDPI
publisher.none.fl_str_mv MDPI
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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