Randomized controlled trial of genotype-guided warfarin anticoagulation in Chinese elderly patients with nonvalvular atrial fibrillation

Randomized controlled trial of genotype-guided warfarin anticoagulation in Chinese elderly patients with nonvalvular atrial fibrillation
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基因型指导华法林抗凝治疗中国老年非瓣膜性房颤患者的随机对照试验

DOI:
10.1111/jcpt.13218
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发表时间:
2020
影响因子:
2
通讯作者:
Liu Jia
Liu Jia
中科院分区:
医学4区
文献类型:
--
作者:
Zhu Ye;Xu Chao;Liu Jia

文献摘要

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What is known and objectiveWarfarin is an oral anticoagulant which has been widely used to treat and prevent thromboembolic events. Managing warfarin therapy requires careful monitoring and dose titration. This randomized controlled study was designed to assess the effect of genotype‐guided warfarin anticoagulation in Chinese elderly patients with nonvalvular atrial fibrillation.Methods507 adults were randomized to receive initial dosing as determined by an algorithm containing genetic (VKORC1andCYP2C9) plus clinical information or only clinical information. The primary endpoint was the time in therapeutic range (TTR) over 90 days. Secondary end points included haemorrhagic events, thrombotic events and mortality.ResultsThe TTR was significantly different between genetic group and control group. The average TTR was (70.80 ± 24.39) % in the genotype‐guided group as compared with (53.44 ± 26.73) % in the control group. This represents a difference of 17.36% (95% CI, 11.82 to 22.89,P< .001). The cumulative incidence of total haemorrhagic events, minor haemorrhagic events, gastrointestinal bleeding and intracerebral bleeding events was not significantly different between two groups (P> .05). Follow‐up showed that the cumulative incidence of ischaemic stroke events occurred in the genetic group was significantly lower than that in the control group (2.39% vs 6.82%), and the genetic group had a significant lower risk than control group in cumulative incidence of ischaemic stroke events [HR 0.22, (95% CI 0.065 to 0.77),P< .05].What is new and conclusionGenotype‐guided dosing could improve the average TTR, and follow‐up result showed that genotype‐guided therapy resulted in a significantly lower risk of ischaemic stroke events. Further research is required to focus on the clinical benefit of genotype‐guided dosing.