a Servicio de Hematología y Oncología Médica, Hospital Universitario Morales Meseguer, Centro Regional de Hemodonación , Universidad de Murcia, IMIB-Arrixaca, CIBERER , Murcia , Spain.
Expert Rev Hematol. 2019 Jun;12(6):397-405. doi: 10.1080/17474086.2019.1611424. Epub 2019 May 22.
. Antithrombin is a serpin that inhibits multiple procoagulant serine proteases and acts as an endogenous anticoagulant. Thus, congenital antithrombin deficiency constitutes a major thrombophilic state, the most severe so far. . In the present work, we globally review the biology, genetics, diagnosis, and management of congenital antithrombin deficiency, and also discuss puzzling questions and future perspectives regarding this severe inherited thrombophilia. . Although this disorder exerts high clinical heterogeneity, many carriers will need careful and long-term anticoagulation and/or thromboprophylaxis, especially in high-risk situations, such as surgery and pregnancy. Notably, antithrombin concentrates constitute a considerable arsenal for both treatment and prevention of acute venous thrombosis in subjects with antithrombin deficiency. Current evidences are based almost exclusively on retrospective case series, so an integrated functional, biochemical and molecular characterization will be of clinical relevance and guide hematologists' personalized decisions.
抗凝血酶是丝氨酸蛋白酶抑制剂超家族中的一员,可抑制多种促凝血酶,发挥内源性抗凝作用。因此,先天性抗凝血酶缺乏构成了一种主要的血栓形成倾向状态,是迄今为止最严重的一种。在本研究中,我们全面回顾了先天性抗凝血酶缺乏的生物学、遗传学、诊断和管理,并讨论了有关这种严重遗传性血栓形成倾向的一些令人困惑的问题和未来展望。尽管这种疾病表现出高度的临床异质性,但许多携带者仍需要仔细和长期的抗凝和/或血栓预防,尤其是在高风险情况下,如手术和妊娠。值得注意的是,抗凝血酶浓缩物是治疗和预防抗凝血酶缺乏症患者急性静脉血栓形成的重要武器。目前的证据几乎完全基于回顾性病例系列,因此,综合的功能、生化和分子特征将具有临床相关性,并指导血液科医生的个体化决策。