Identification of environmental and genetic factors that influence warfarin time in therapeutic range

Detalhes bibliográficos
Autor(a) principal: Botton, Mariana Rodrigues
Data de Publicação: 2020
Outros Autores: Viola, Patrícia Pacheco, Meireles, Mariana Rost, Bruxel, Estela Maria, Zuchinali, Priccila, Bandinelli, Eliane, Rohde, Luis Eduardo Paim, Leiria, Tiago Luiz Luz, Salamoni, Joyce Yukie Yamakawa, Garbin, Arthur Pereira, Hutz, Mara Helena
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/267096
Resumo: Warfarin is an oral anticoagulant prescribed to prevent and treat thromboembolic disorders. It has a narrow therapeutic window and must have its effect controlled. Prothrombin test, expressed in INR value, is used for dose management. Time in therapeutic range (TTR) is an important outcome of quality control of anticoagulation therapy and is influenced by several factors. The aim of this study was to identify genetic, demographic, and clinical factors that can potentially influence TTR. In total,422 patients using warfarin were investigated. Glibenclamide co-medication and presence of CYP2C9*2 and/or *3 alleles were associated with higher TTR, while amiodarone, acetaminophen and verapamil co-medication were associated with lower TTR. Our data suggest that TTR is influenced by co-medication and genetic factors. Thus, individuals in use of glibenclamide may need a more careful monitoring and genetic testing (CYP2C9*2 and/or *3 alleles) may improve the anticoagulation management. In addition, in order to reach and maintain the INR in the target for a longer period, it is better to discuss dose adjustment in office instead of by telephone assessment. Other studies are needed to confirm these results and to find more variables that could contribute to this important parameter.
id UFRGS-2_988f52ce9d3520fc17fbb3f3524af508
oai_identifier_str oai:www.lume.ufrgs.br:10183/267096
network_acronym_str UFRGS-2
network_name_str Repositório Institucional da UFRGS
repository_id_str
spelling Botton, Mariana RodriguesViola, Patrícia PachecoMeireles, Mariana RostBruxel, Estela MariaZuchinali, PriccilaBandinelli, ElianeRohde, Luis Eduardo PaimLeiria, Tiago Luiz LuzSalamoni, Joyce Yukie YamakawaGarbin, Arthur PereiraHutz, Mara Helena2023-11-14T03:23:29Z20201415-4757http://hdl.handle.net/10183/267096001158568Warfarin is an oral anticoagulant prescribed to prevent and treat thromboembolic disorders. It has a narrow therapeutic window and must have its effect controlled. Prothrombin test, expressed in INR value, is used for dose management. Time in therapeutic range (TTR) is an important outcome of quality control of anticoagulation therapy and is influenced by several factors. The aim of this study was to identify genetic, demographic, and clinical factors that can potentially influence TTR. In total,422 patients using warfarin were investigated. Glibenclamide co-medication and presence of CYP2C9*2 and/or *3 alleles were associated with higher TTR, while amiodarone, acetaminophen and verapamil co-medication were associated with lower TTR. Our data suggest that TTR is influenced by co-medication and genetic factors. Thus, individuals in use of glibenclamide may need a more careful monitoring and genetic testing (CYP2C9*2 and/or *3 alleles) may improve the anticoagulation management. In addition, in order to reach and maintain the INR in the target for a longer period, it is better to discuss dose adjustment in office instead of by telephone assessment. Other studies are needed to confirm these results and to find more variables that could contribute to this important parameter.application/pdfengGenetics and molecular biology. Ribeirão Preto. Vol. 43, no. 1 suppl. 2 (2020), e20190025, 5p.VarfarinaCYP2C9VKORC1ASPHTTRIdentification of environmental and genetic factors that influence warfarin time in therapeutic rangeinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001158568.pdf.txt001158568.pdf.txtExtracted Texttext/plain0http://www.lume.ufrgs.br/bitstream/10183/267096/2/001158568.pdf.txtd41d8cd98f00b204e9800998ecf8427eMD52ORIGINAL001158568.pdfTexto completo (inglês)application/pdf9023513http://www.lume.ufrgs.br/bitstream/10183/267096/1/001158568.pdfc26f90d63e539bb3ab12260add46adb6MD5110183/2670962023-11-15 04:25:57.166108oai:www.lume.ufrgs.br:10183/267096Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-11-15T06:25:57Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Identification of environmental and genetic factors that influence warfarin time in therapeutic range
title Identification of environmental and genetic factors that influence warfarin time in therapeutic range
spellingShingle Identification of environmental and genetic factors that influence warfarin time in therapeutic range
Botton, Mariana Rodrigues
Varfarina
CYP2C9
VKORC1
ASPH
TTR
title_short Identification of environmental and genetic factors that influence warfarin time in therapeutic range
title_full Identification of environmental and genetic factors that influence warfarin time in therapeutic range
title_fullStr Identification of environmental and genetic factors that influence warfarin time in therapeutic range
title_full_unstemmed Identification of environmental and genetic factors that influence warfarin time in therapeutic range
title_sort Identification of environmental and genetic factors that influence warfarin time in therapeutic range
author Botton, Mariana Rodrigues
author_facet Botton, Mariana Rodrigues
Viola, Patrícia Pacheco
Meireles, Mariana Rost
Bruxel, Estela Maria
Zuchinali, Priccila
Bandinelli, Eliane
Rohde, Luis Eduardo Paim
Leiria, Tiago Luiz Luz
Salamoni, Joyce Yukie Yamakawa
Garbin, Arthur Pereira
Hutz, Mara Helena
author_role author
author2 Viola, Patrícia Pacheco
Meireles, Mariana Rost
Bruxel, Estela Maria
Zuchinali, Priccila
Bandinelli, Eliane
Rohde, Luis Eduardo Paim
Leiria, Tiago Luiz Luz
Salamoni, Joyce Yukie Yamakawa
Garbin, Arthur Pereira
Hutz, Mara Helena
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Botton, Mariana Rodrigues
Viola, Patrícia Pacheco
Meireles, Mariana Rost
Bruxel, Estela Maria
Zuchinali, Priccila
Bandinelli, Eliane
Rohde, Luis Eduardo Paim
Leiria, Tiago Luiz Luz
Salamoni, Joyce Yukie Yamakawa
Garbin, Arthur Pereira
Hutz, Mara Helena
dc.subject.por.fl_str_mv Varfarina
topic Varfarina
CYP2C9
VKORC1
ASPH
TTR
dc.subject.eng.fl_str_mv CYP2C9
VKORC1
ASPH
TTR
description Warfarin is an oral anticoagulant prescribed to prevent and treat thromboembolic disorders. It has a narrow therapeutic window and must have its effect controlled. Prothrombin test, expressed in INR value, is used for dose management. Time in therapeutic range (TTR) is an important outcome of quality control of anticoagulation therapy and is influenced by several factors. The aim of this study was to identify genetic, demographic, and clinical factors that can potentially influence TTR. In total,422 patients using warfarin were investigated. Glibenclamide co-medication and presence of CYP2C9*2 and/or *3 alleles were associated with higher TTR, while amiodarone, acetaminophen and verapamil co-medication were associated with lower TTR. Our data suggest that TTR is influenced by co-medication and genetic factors. Thus, individuals in use of glibenclamide may need a more careful monitoring and genetic testing (CYP2C9*2 and/or *3 alleles) may improve the anticoagulation management. In addition, in order to reach and maintain the INR in the target for a longer period, it is better to discuss dose adjustment in office instead of by telephone assessment. Other studies are needed to confirm these results and to find more variables that could contribute to this important parameter.
publishDate 2020
dc.date.issued.fl_str_mv 2020
dc.date.accessioned.fl_str_mv 2023-11-14T03:23:29Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/other
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/267096
dc.identifier.issn.pt_BR.fl_str_mv 1415-4757
dc.identifier.nrb.pt_BR.fl_str_mv 001158568
identifier_str_mv 1415-4757
001158568
url http://hdl.handle.net/10183/267096
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.pt_BR.fl_str_mv Genetics and molecular biology. Ribeirão Preto. Vol. 43, no. 1 suppl. 2 (2020), e20190025, 5p.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Repositório Institucional da UFRGS
collection Repositório Institucional da UFRGS
bitstream.url.fl_str_mv http://www.lume.ufrgs.br/bitstream/10183/267096/2/001158568.pdf.txt
http://www.lume.ufrgs.br/bitstream/10183/267096/1/001158568.pdf
bitstream.checksum.fl_str_mv d41d8cd98f00b204e9800998ecf8427e
c26f90d63e539bb3ab12260add46adb6
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)
repository.mail.fl_str_mv
_version_ 1801225103928721408