使用华法林的心房颤动患者的CYP2C9*2、CYP2C9*3和VKORC1基因多态性与治疗范围内的时间相关。

IF 2.6 Q2 GENETICS & HEREDITY
Application of Clinical Genetics Pub Date : 2019-08-02 eCollection Date: 2019-01-01 DOI:10.2147/TACG.S197316
Maria Mariana Barros Melo da Silveira, Leiliandry de Araújo Melo, Filipe Maia Ferreira Gomes, Leonardo José de Cupertino Barreto da Rocha Andrade, Isabela Paulino Serur, Isabelle Cecília de Vasconcellos Piscoya, Raposo Marina Gueiros, Kleyton Palmeira do Ó, Raul Emídio de Lima, Victor Arthur Eulálio Brasileiro, Luydson Richardson Silva Vasconcelos, Dário Celestino Sobral Filho
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引用次数: 0

摘要

引言:华法林仍然是世界各地临床实践中应用最广泛的抗凝剂,用于预防心房颤动(AF)患者的血栓栓塞事件。通过治疗范围内的时间(TTR)来评估抗凝控制的质量,被认为是评估抗凝质量的好方法。TTR的变异性可以通过CYP2C9和VKORC1基因变异的存在来解释。方法:本研究通过TTR检测了心房颤动患者CYP2C9和VKORC1基因多态性与口服抗凝控制之间的关系。在队列随访中进行了横断面研究。这项研究包括317名使用华法林的房颤患者,他们接受了一年的随访。CYP2C9(rs1057910)、(rs1799853)和VKORC1(rs923231)基因的基因分型是使用TaqMan探针通过实时PCR进行的。结果:CYP2C9*3基因(rs1057910)变异基因型患者的TTR(TTR 81-100%)高于p=0.005和p=0.002。关于VKORC1(rs923231),与p分别为0.005和0.004的患者相比,具有VKORC1(rss923231)基因变异基因型的患者也表现出更高的TTR(TTR 81-100%)。在多变量模型中,VKORC1(rs923231)与TTR组的比较仍然相关(p=0.01;46-60%与81-100%组,p=0.01)。结论:在巴西东北部使用华法林的AF患者中,CYP2C9*3(AA)和VKORC1-1639(GG)基因型与最差的抗凝控制(TTR)质量相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Polymorphisms of <i>CYP2C9*2, CYP2C9*3</i> and <i>VKORC1</i> genes related to time in therapeutic range in patients with atrial fibrillation using warfarin.

Polymorphisms of CYP2C9*2, CYP2C9*3 and VKORC1 genes related to time in therapeutic range in patients with atrial fibrillation using warfarin.

Introduction: Warfarin continues to be the most widely used anticoagulant in clinical practice around the world for the prevention of thromboembolic events in patients with atrial fibrillation (AF). The evaluation of the quality of anticoagulation control, estimated by time in therapeutic range (TTR), is accepted as a good method to evaluate the quality of anticoagulation. The variability of TTR can be explained by the presence of variants of the CYP2C9 and VKORC1 genes.

Methods: This study examined the association between polymorphisms of the CYP2C9 and VKORC1 genes and control of oral anticoagulation, through TTR, in patients with AF. A cross-sectional study was conducted within a cohort follow-up. The study comprised of 317 patients with AF, using warfarin, who were followed up for one year. The genotyping of genes CYP2C9 (rs1057910), (rs1799853) and VKORC1 (rs923231) was performed by PCR in real time, using TaqMan probes.

Results: Patients who had variant genotypes for the CYP2C9*3 gene (rs1057910) presented higher TTR (TTR 81-100%) when compared to when compared to the <45% and 46-60% TTR groups (p=0.005 and p=0.002, respectively). Regarding VKORC1 (rs923231), patients who had the variant genotype for the VKORC1 (rs923231) gene also presented a higher TTR (TTR 81-100%), when when compared to the <45% and 46-60% TTR groups (p=0.005 and p=0.004, respectively). In a multivariate model, VKORC1 (rs923231) remained associated for comparisons with the TTR groups (<45% vs 81-100% groups, p=0.01; and 46-60% vs 81-100% groups, p=0.01).

Conclusion: The genotypes of the CYP2C9*3 (AA) and VKORC1 -1639 (GG) genes were associated with the worst quality of anticoagulation control (TTR) in patients with AF using warfarin in the northeast of Brazil.

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来源期刊
Application of Clinical Genetics
Application of Clinical Genetics Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
5.40
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审稿时长
16 weeks
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