The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use

Background/Aim. A single nucleotide polymorphism c.- 1639G>A in the promoter region of vitamin K-epoxide reductase (VKORC1) gene has been found to account for most of the variability in response to oral anticoagulants (OA). The aim of the study was to determine the incidence and the effect of...

Full description

Bibliographic Details
Main Authors: Kovač Mirjana, Rakićević Ljiljana, Maslać Aleksandar, Radojković Dragica
Format: Article
Language:English
Published: Military Health Department, Ministry of Defance, Serbia 2009-01-01
Series:Vojnosanitetski Pregled
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0042-8450/2009/0042-84500908617K.pdf
_version_ 1818108272948805632
author Kovač Mirjana
Rakićević Ljiljana
Maslać Aleksandar
Radojković Dragica
author_facet Kovač Mirjana
Rakićević Ljiljana
Maslać Aleksandar
Radojković Dragica
author_sort Kovač Mirjana
collection DOAJ
description Background/Aim. A single nucleotide polymorphism c.- 1639G>A in the promoter region of vitamin K-epoxide reductase (VKORC1) gene has been found to account for most of the variability in response to oral anticoagulants (OA). The aim of the study was to determine the incidence and the effect of c.-1639G>A polymorphism on the acenocoumarol dosage requirements in the group of patients under stable anticoagulation, and to estimate the variability in response to OA. Methods. Our study included 200 consecutive patients requiring low (n = 43), medium (n = 127) and high (n = 30) acenocoumarol dose. Results. Out of 43 low dose patients, 40 (93 %) carried the A allele. The A allele was less frequent in the group of 30 patients requiring high dose: among these patients 13 (43.3%) carried the A allele in the heterozygous form and none of them carried AA genotype. The patients with GG genotype required 2.6 times higher dose than the patients carriers of AA genotype (p < 0.0001). In 33 patients (16.5%) the overdose occurred during the initiation of anticoagulant therapy and in 11 patients (5.5%) it was associated with bleeding. Out of the group of 33 overdosed patients, 27 and 6 patients carried AA and GA genotype, respectively (p < 0.000001). Conclusion. VKORC1 significantly influenced OA dose and predicted individuals predisposed to unstable anticoagulation. The carriers of AA genotype required 2.6 time lower doses of OA than the carriares of GG genotype. Pharmacogenetic testing could predict a high risk of overdose among 28.5 % of our patients - carriers of AA genotype, before anticoagulation therapy initiation.
first_indexed 2024-12-11T02:12:44Z
format Article
id doaj.art-03b9659385c443f5a6446b16d56351dd
institution Directory Open Access Journal
issn 0042-8450
language English
last_indexed 2024-12-11T02:12:44Z
publishDate 2009-01-01
publisher Military Health Department, Ministry of Defance, Serbia
record_format Article
series Vojnosanitetski Pregled
spelling doaj.art-03b9659385c443f5a6446b16d56351dd2022-12-22T01:24:14ZengMilitary Health Department, Ministry of Defance, SerbiaVojnosanitetski Pregled0042-84502009-01-0166861762110.2298/VSP0908617KThe c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants useKovač MirjanaRakićević LjiljanaMaslać AleksandarRadojković DragicaBackground/Aim. A single nucleotide polymorphism c.- 1639G>A in the promoter region of vitamin K-epoxide reductase (VKORC1) gene has been found to account for most of the variability in response to oral anticoagulants (OA). The aim of the study was to determine the incidence and the effect of c.-1639G>A polymorphism on the acenocoumarol dosage requirements in the group of patients under stable anticoagulation, and to estimate the variability in response to OA. Methods. Our study included 200 consecutive patients requiring low (n = 43), medium (n = 127) and high (n = 30) acenocoumarol dose. Results. Out of 43 low dose patients, 40 (93 %) carried the A allele. The A allele was less frequent in the group of 30 patients requiring high dose: among these patients 13 (43.3%) carried the A allele in the heterozygous form and none of them carried AA genotype. The patients with GG genotype required 2.6 times higher dose than the patients carriers of AA genotype (p < 0.0001). In 33 patients (16.5%) the overdose occurred during the initiation of anticoagulant therapy and in 11 patients (5.5%) it was associated with bleeding. Out of the group of 33 overdosed patients, 27 and 6 patients carried AA and GA genotype, respectively (p < 0.000001). Conclusion. VKORC1 significantly influenced OA dose and predicted individuals predisposed to unstable anticoagulation. The carriers of AA genotype required 2.6 time lower doses of OA than the carriares of GG genotype. Pharmacogenetic testing could predict a high risk of overdose among 28.5 % of our patients - carriers of AA genotype, before anticoagulation therapy initiation.http://www.doiserbia.nb.rs/img/doi/0042-8450/2009/0042-84500908617K.pdfpolymorphism, geneticanticoagulantsdose response relationshipdrug utilization
spellingShingle Kovač Mirjana
Rakićević Ljiljana
Maslać Aleksandar
Radojković Dragica
The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
Vojnosanitetski Pregled
polymorphism, genetic
anticoagulants
dose response relationship
drug utilization
title The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
title_full The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
title_fullStr The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
title_full_unstemmed The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
title_short The c.-1639g>A polymorphism of the VKORC1 gene and his influence on the therapeutic response during oral anticoagulants use
title_sort c 1639g gt a polymorphism of the vkorc1 gene and his influence on the therapeutic response during oral anticoagulants use
topic polymorphism, genetic
anticoagulants
dose response relationship
drug utilization
url http://www.doiserbia.nb.rs/img/doi/0042-8450/2009/0042-84500908617K.pdf
work_keys_str_mv AT kovacmirjana thec1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT rakicevicljiljana thec1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT maslacaleksandar thec1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT radojkovicdragica thec1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT kovacmirjana c1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT rakicevicljiljana c1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT maslacaleksandar c1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse
AT radojkovicdragica c1639ggtapolymorphismofthevkorc1geneandhisinfluenceonthetherapeuticresponseduringoralanticoagulantsuse