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作为新型抗凝剂靶点的因子XI和因子XII。

Factors XI and XII as Targets for New Anticoagulants.

作者信息

Weitz Jeffrey I, Fredenburgh James C

机构信息

Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, ON, Canada; Department of Medicine, McMaster University, Hamilton, ON, Canada; The Thrombosis and Atherosclerosis Research Institute, McMaster University, Hamilton, ON, Canada.

Department of Medicine, McMaster University, Hamilton, ON, Canada; The Thrombosis and Atherosclerosis Research Institute, McMaster University, Hamilton, ON, Canada.

出版信息

Front Med (Lausanne). 2017 Feb 24;4:19. doi: 10.3389/fmed.2017.00019. eCollection 2017.

Abstract

Compared with vitamin K antagonists, the direct oral anticoagulants (DOACs) are simpler to administer and are associated with less intracranial bleeding. Nonetheless, even with the DOACs, bleeding still occurs and many patients with atrial fibrillation fail to receive anticoagulant thromboprophylaxis because of the fear of bleeding. Therefore, there is an urgent need for safer anticoagulants. Recent investigations into the biochemistry of hemostasis and thrombosis have identified new targets for development of novel anticoagulants. Using data from complementary sources, including epidemiological studies and investigations in various animal models, the contact pathway has emerged as a potential mediator of thrombosis that plays a minor part in hemostasis. Consequently, factor (F) XII of the contact system and FXI in the intrinsic pathway have been identified as potentially safer targets of anticoagulation than thrombin or FXa. However, further studies are needed to identify which is the better target for the appropriate indication. This review highlights the evidence for focusing on FXI and FXII and examines the novel approaches directed at these new targets. These emerging strategies should address current unmet medical needs and provide new avenues by which to improve anticoagulant therapy by reducing the risk of bleeding.

摘要

与维生素K拮抗剂相比,直接口服抗凝剂(DOACs)服用更简便,且颅内出血风险更低。尽管如此,即便使用DOACs,出血情况仍会发生,而且许多房颤患者因担心出血而未接受抗凝血栓预防治疗。因此,迫切需要更安全的抗凝剂。最近对止血和血栓形成生物化学的研究确定了新型抗凝剂开发的新靶点。利用包括流行病学研究和各种动物模型研究在内的补充来源的数据,接触途径已成为血栓形成的潜在介质,在止血中起次要作用。因此,接触系统的因子(F)XII和内源性途径中的FXI已被确定为比凝血酶或FXa更具潜在安全性的抗凝靶点。然而,需要进一步研究以确定针对合适适应症哪个靶点更佳。本综述强调了聚焦于FXI和FXII的证据,并探讨了针对这些新靶点的新方法。这些新兴策略应满足当前未满足的医疗需求,并通过降低出血风险提供改善抗凝治疗的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2958/5323386/248ff0a318e9/fmed-04-00019-g001.jpg

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