Chan Noel, Carlin Stephanie, Hirsh Jack
Population Health Research Institute, Hamilton, Ontario, Canada; Thrombosis and Atherosclerosis Research Institute, Hamilton, Ontario, Canada; Division of Hematology and Thromboembolism, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Division of Hematology and Thromboembolism, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Pharmacol Rev. 2025 Mar;77(2):100037. doi: 10.1016/j.pharmr.2025.100037. Epub 2025 Jan 7.
Taking a historical perspective, we review the discovery, pharmacology, and clinical evaluation of the old and new anticoagulants that have been approved for clinical use. The drugs are discussed chronologically, starting in the 1880s, and progressing through to 2024. The innovations in technology used to develop novel anticoagulants came in fits and starts and reflected the advances in science and technology over these decades, whereas the shift from anecdote to evidence-based use of anticoagulants was delayed until the principles of epidemiology and biostatistics were introduced into clinical trial design and to the approval process. Hirudin, heparin, and vitamin K antagonists were discovered by chance, and were used clinically before their mechanism of action was elucidated and before their net clinical benefits were evaluated in randomized clinical trials. Subsequent anticoagulants were designed based on a better understanding of the structure and function of coagulation proteins, including antithrombin, thrombin, and factor Xa, and underwent more rigorous preclinical and clinical evaluation before regulatory approval. By simplifying oral anticoagulation, the direct oral anticoagulants have revolutionized anticoagulation care and have enhanced the uptake of anticoagulation, but bleeding has not been eliminated and there is a need for more effective and convenient anticoagulants for thrombosis triggered by the contact pathway of coagulation. The newly developed factor XIa and XIIa inhibitors have the potential to address these unmet clinical needs and are undergoing clinical evaluation for several indications. SIGNIFICANCE STATEMENT: Anticoagulant therapy is the cornerstone of treatment and prevention of thrombosis, which remains a leading cause of morbidity and mortality worldwide. Elucidation of the structure and function of coagulation enzymes, their cofactors, and inhibitors, coupled with advances in structure-based design led to the discovery of more convenient, safer, and more effective anticoagulants that have revolutionized the management of thrombotic disorders.
从历史角度出发,我们回顾了已获批用于临床的新旧抗凝剂的发现、药理学及临床评估。这些药物按时间顺序进行讨论,始于19世纪80年代,一直延续到2024年。用于开发新型抗凝剂的技术创新断断续续出现,反映了这几十年间的科技进步,而抗凝剂从轶事性使用向基于证据的使用的转变则推迟到流行病学和生物统计学原理被引入临床试验设计及审批流程之后。水蛭素、肝素和维生素K拮抗剂是偶然发现的,在其作用机制被阐明以及在随机临床试验中评估其净临床益处之前就已用于临床。后续的抗凝剂是在对凝血蛋白(包括抗凝血酶、凝血酶和因子Xa)的结构和功能有了更好理解的基础上设计的,并在监管批准之前接受了更严格的临床前和临床评估。直接口服抗凝剂通过简化口服抗凝治疗,彻底改变了抗凝治疗模式并提高了抗凝治疗的接受度,但出血问题并未消除,对于由凝血接触途径引发的血栓形成,仍需要更有效、更方便的抗凝剂。新开发的因子XIa和XIIa抑制剂有潜力满足这些未被满足的临床需求,目前正在针对多种适应症进行临床评估。重要声明:抗凝治疗是血栓形成治疗和预防的基石,血栓形成仍是全球发病和死亡的主要原因。对凝血酶、其辅因子和抑制剂的结构与功能的阐明,以及基于结构设计的进展,促使人们发现了更方便、更安全、更有效的抗凝剂,彻底改变了血栓性疾病的管理方式。