Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway.
Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway; Department of Cardiology, Oslo University Hospital Ullevål, Norway.
Thromb Res. 2022 Jun;214:53-62. doi: 10.1016/j.thromres.2022.04.013. Epub 2022 Apr 25.
In this review, we give an overview over observational and experimental studies supporting factors XI and XII as targets for anticoagulant therapy. The majority of observational studies on FXI report low concentrations of FXI to be protective against ischemic stroke and venous thrombosis. There is also extensive evidence from experimental and animal studies supporting FXI inhibition as a target for anticoagulant therapy, alone or in combination with other antithrombotic treatments. Four Phase 2 clinical trials on patients undergoing total knee arthroplasty showed non-inferiority or superiority of FXI inhibition compared to enoxaparin for the primary outcome, which was incidence of venous thromboembolism. One Phase 2 trial reported that FXI inhibition is associated with fewer bleeding events than apixaban. The results from observational studies on FXII are more conflicting. Some show that low FXII concentrations confer protection against thrombosis, while others have found it to be deleterious. Results from experimental studies are inconclusive, but suggest that FXII inhibition might be useful in preventing thrombosis caused by foreign objects like catheters or mechanical heart valves. One Phase 2 study not conducted on thrombosis has reported FXII inhibition as safe. In conclusion, FXI seems to be a promising target for antithrombotic therapy, both alone and in combination with existing therapies, while the potential of targeting FXII is still unclear.
在这篇综述中,我们概述了支持因子 XI 和因子 XII 作为抗凝治疗靶点的观察性和实验性研究。大多数关于 FXI 的观察性研究报告称,FXI 浓度较低可预防缺血性卒中和静脉血栓形成。实验和动物研究也提供了广泛的证据,支持 FXI 抑制作为抗凝治疗的靶点,单独或与其他抗血栓治疗联合使用。四项针对接受全膝关节置换术患者的 2 期临床试验表明,与依诺肝素相比,FXI 抑制在主要结局(即静脉血栓栓塞事件发生率)方面具有非劣效性或优越性。一项 2 期试验报告称,FXI 抑制与较少的出血事件相关,而出血事件是与 apixaban 相关的。关于 FXII 的观察性研究结果更为矛盾。一些研究表明,低 FXII 浓度可预防血栓形成,而其他研究则发现 FXII 具有有害作用。实验研究结果尚无定论,但表明 FXII 抑制可能有助于预防导管或机械心脏瓣膜等异物引起的血栓形成。一项未在血栓形成患者中进行的 2 期研究报告称,FXI 抑制是安全的。总之,FXI 似乎是一种有前途的抗血栓治疗靶点,无论是单独使用还是与现有治疗方法联合使用,而靶向 FXII 的潜力尚不清楚。