抗凝剂:从偶然发现到基于结构的设计。

IF 19.3 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Pharmacological Reviews Pub Date : 2025-03-01 Epub Date: 2025-01-07 DOI:10.1016/j.pharmr.2025.100037
Noel Chan, Stephanie Carlin, Jack Hirsh
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引用次数: 0

摘要

从历史的角度,我们回顾发现,药理学和临床评价的新老抗凝剂已批准用于临床应用。这些药物是按时间顺序讨论的,从19世纪80年代开始,一直到2024年。用于开发新型抗凝剂的技术创新时断时续,反映了近几十年来科学技术的进步,而抗凝剂从轶事到循证使用的转变被推迟了,直到流行病学和生物统计学的原则被引入临床试验设计和批准过程。水蛭素、肝素和维生素K拮抗剂是偶然发现的,在它们的作用机制被阐明和它们的净临床效益在随机临床试验中被评估之前就被临床使用。随后的抗凝药物是在更好地了解凝血蛋白(包括抗凝血酶、凝血酶和Xa因子)的结构和功能的基础上设计的,并在监管部门批准前进行了更严格的临床前和临床评估。通过简化口服抗凝,直接口服抗凝剂彻底改变了抗凝护理,提高了抗凝剂的吸收,但出血并没有消除,对于凝血接触途径引发的血栓形成,需要更有效、更方便的抗凝剂。新开发的因子XIa和XIIa抑制剂有可能解决这些未满足的临床需求,并且正在进行几种适应症的临床评估。意义声明:抗凝治疗是治疗和预防血栓形成的基石,它仍然是世界范围内发病率和死亡率的主要原因。凝血酶及其辅助因子和抑制剂的结构和功能的阐明,加上基于结构的设计的进步,导致了更方便、更安全、更有效的抗凝剂的发现,这些抗凝剂已经彻底改变了血栓性疾病的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticoagulants: From chance discovery to structure-based design.

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.

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来源期刊
Pharmacological Reviews
Pharmacological Reviews 医学-药学
CiteScore
34.70
自引率
0.50%
发文量
40
期刊介绍: Pharmacological Reviews is a highly popular and well-received journal that has a long and rich history of success. It was first published in 1949 and is currently published bimonthly online by the American Society for Pharmacology and Experimental Therapeutics. The journal is indexed or abstracted by various databases, including Biological Abstracts, BIOSIS Previews Database, Biosciences Information Service, Current Contents/Life Sciences, EMBASE/Excerpta Medica, Index Medicus, Index to Scientific Reviews, Medical Documentation Service, Reference Update, Research Alerts, Science Citation Index, and SciSearch. Pharmacological Reviews offers comprehensive reviews of new pharmacological fields and is able to stay up-to-date with published content. Overall, it is highly regarded by scholars.
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