Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos

Background: The dose of oral anticoagulants (OAC) shows great variability among patients. Pharmacogenetic studies have shown that common variants in genes CYP2C9 (*2 and *3) and VKORC1 (-1639G>A) are associated with lower requirements of OAC. Aim: To study the association between average maintena...

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Autores principales: Benavides,Felipe, Grossman,Nicole, Poggi,Helena, Nieto,Elena, Bertrán,Antonio, Araos,Daniel, Vásquez,Marcos, Ibarra,Ignaz, Cáceres,Felipe, Espinoza,Karena, Lagos,Marcela, Repetto M,Gabriela
Lenguaje:Spanish / Castilian
Publicado: Sociedad Médica de Santiago 2015
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015001100001
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spelling oai:scielo:S0034-988720150011000012016-01-19Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenosBenavides,FelipeGrossman,NicolePoggi,HelenaNieto,ElenaBertrán,AntonioAraos,DanielVásquez,MarcosIbarra,IgnazCáceres,FelipeEspinoza,KarenaLagos,MarcelaRepetto M,Gabriela Acenocoumarol Cytochrome P-450 CYP2C Pharmacogenetics VKORC1, protein, human Warfarin Background: The dose of oral anticoagulants (OAC) shows great variability among patients. Pharmacogenetic studies have shown that common variants in genes CYP2C9 (*2 and *3) and VKORC1 (-1639G>A) are associated with lower requirements of OAC. Aim: To study the association between average maintenance doses of oral anticoagulant therapy required to maintain a stable INR and CYP2C9 and VKORC1 gene variants in Chilean adults. Material and Methods: Prospective study of patients on anticoagulant treatment and with a stable international normalized ratio (INR) for prothrombin time for at least three months. Patients were classified as having high or low acenocoumarol or warfarin requirements. Peripheral blood DNA genotyping was performed by polymerase chain reaction and restriction fragment polymorphism or sequencing and electrophoresis. Results: The study included 185 patients, 125 on acenocoumarol and 60 on warfarin. Patients with VKORC1-1639A allele were more likely to require lower doses of both drugs than patients with the G allele (Odds ratio [OR] for acenocoumarol 9.06, and OR for warfarin = 18.7). There was no association between CYP2C9*2 and*3 and acenocoumarol or warfarin requirements. Conclusions: There is an association between VKORC1-1639A variant and anticoagulant doses.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.143 n.11 20152015-11-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015001100001es10.4067/S0034-98872015001100001
institution Scielo Chile
collection Scielo Chile
language Spanish / Castilian
topic Acenocoumarol
Cytochrome P-450 CYP2C
Pharmacogenetics
VKORC1, protein, human
Warfarin
spellingShingle Acenocoumarol
Cytochrome P-450 CYP2C
Pharmacogenetics
VKORC1, protein, human
Warfarin
Benavides,Felipe
Grossman,Nicole
Poggi,Helena
Nieto,Elena
Bertrán,Antonio
Araos,Daniel
Vásquez,Marcos
Ibarra,Ignaz
Cáceres,Felipe
Espinoza,Karena
Lagos,Marcela
Repetto M,Gabriela
Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
description Background: The dose of oral anticoagulants (OAC) shows great variability among patients. Pharmacogenetic studies have shown that common variants in genes CYP2C9 (*2 and *3) and VKORC1 (-1639G>A) are associated with lower requirements of OAC. Aim: To study the association between average maintenance doses of oral anticoagulant therapy required to maintain a stable INR and CYP2C9 and VKORC1 gene variants in Chilean adults. Material and Methods: Prospective study of patients on anticoagulant treatment and with a stable international normalized ratio (INR) for prothrombin time for at least three months. Patients were classified as having high or low acenocoumarol or warfarin requirements. Peripheral blood DNA genotyping was performed by polymerase chain reaction and restriction fragment polymorphism or sequencing and electrophoresis. Results: The study included 185 patients, 125 on acenocoumarol and 60 on warfarin. Patients with VKORC1-1639A allele were more likely to require lower doses of both drugs than patients with the G allele (Odds ratio [OR] for acenocoumarol 9.06, and OR for warfarin = 18.7). There was no association between CYP2C9*2 and*3 and acenocoumarol or warfarin requirements. Conclusions: There is an association between VKORC1-1639A variant and anticoagulant doses.
author Benavides,Felipe
Grossman,Nicole
Poggi,Helena
Nieto,Elena
Bertrán,Antonio
Araos,Daniel
Vásquez,Marcos
Ibarra,Ignaz
Cáceres,Felipe
Espinoza,Karena
Lagos,Marcela
Repetto M,Gabriela
author_facet Benavides,Felipe
Grossman,Nicole
Poggi,Helena
Nieto,Elena
Bertrán,Antonio
Araos,Daniel
Vásquez,Marcos
Ibarra,Ignaz
Cáceres,Felipe
Espinoza,Karena
Lagos,Marcela
Repetto M,Gabriela
author_sort Benavides,Felipe
title Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
title_short Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
title_full Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
title_fullStr Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
title_full_unstemmed Efecto de las variantes de VKORC1 y CYP2C9 sobre la dosis de anticoagulantes orales en individuos chilenos
title_sort efecto de las variantes de vkorc1 y cyp2c9 sobre la dosis de anticoagulantes orales en individuos chilenos
publisher Sociedad Médica de Santiago
publishDate 2015
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872015001100001
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