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血管性血友病因子作为口服抗凝药物治疗患者死亡率、心血管事件和出血并发症的标志物。

von Willebrand activation factor as a marker of mortality, cardiovascular events, and bleeding complications in patients treated with oral anticoagulants.

机构信息

Department of Public Health and Clinical Medicine, Skellefteå Research Unit, Umeå University, Umeå, Sweden.

Department of Public Health and Clinical Medicine, Skellefteå Research Unit, Umeå University, Umeå, Sweden.

出版信息

Thromb Res. 2015 Nov;136(5):878-82. doi: 10.1016/j.thromres.2015.08.016. Epub 2015 Aug 28.

Abstract

BACKGROUND

Serious bleeding is a frequent and feared treatment complication in patients treated with oral anticoagulants (OACs). Levels of von Willebrand factor (VWF) antigen have been linked to the risk of bleeding complications, mortality, and cardiovascular events.

OBJECTIVES

In this longitudinal cohort study of evaluating patients treated with OACs, we aimed to evaluate the relationship between VWF displaying a glycoprotein Ib binding conformation (VWF activation factor) and the risk of cardiovascular events, bleeding complications, or all-cause mortality.

MATERIALS AND METHODS

Blood samples were collected at baseline in 356 patients on OACs. Patients were followed for an average of 48 months and bleeding complications leading to admission to hospital or death, cardiovascular events (myocardial infarction, ischemic stroke, and peripheral arterial emboli), and all-cause mortality were recorded and classified.

RESULTS

During the study period, 47 bleeding complications, 84 cardiovascular events, and 97 deaths occurred. In multivariate Cox regression analyses, VWF activation factor was significantly associated with all-cause mortality (HR 1.62; 95% CI: 1.25-2.08) and cardiovascular events (HR 1.28; 95% CI: 1.01-1.63). There was no association observed between VWF activation factor and bleeding complications.

CONCLUSIONS

Patients with high levels of VWF activation factor had an increased risk of cardiovascular events and all-cause mortality during OAC treatment. The selectivity for thrombotic complications adds to the potential value of VWF activation factor as a biomarker or pharmacological target.

摘要

背景

严重出血是接受口服抗凝剂(OAC)治疗的患者经常发生且令人担忧的治疗并发症。血管性血友病因子(VWF)抗原水平与出血并发症、死亡率和心血管事件的风险相关。

目的

在这项评估接受 OAC 治疗的患者的纵向队列研究中,我们旨在评估 VWF 展示糖蛋白 Ib 结合构象(VWF 激活因子)与心血管事件、出血并发症或全因死亡率风险之间的关系。

材料和方法

在 356 名接受 OAC 治疗的患者的基线时采集血液样本。患者平均随访 48 个月,记录和分类导致住院或死亡的出血并发症、心血管事件(心肌梗死、缺血性卒中和外周动脉栓塞)和全因死亡率。

结果

在研究期间,发生了 47 例出血并发症、84 例心血管事件和 97 例死亡。在多变量 Cox 回归分析中,VWF 激活因子与全因死亡率(HR 1.62;95%CI:1.25-2.08)和心血管事件(HR 1.28;95%CI:1.01-1.63)显著相关。VWF 激活因子与出血并发症之间没有观察到相关性。

结论

在 OAC 治疗期间,VWF 激活因子水平较高的患者发生心血管事件和全因死亡率的风险增加。对血栓并发症的选择性增加了 VWF 激活因子作为生物标志物或药物靶点的潜在价值。

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