Autoimmune Diseases Research Unit, Biocruces Bizkaia Health Research Institute, The Basque Country, Bizkaia, Spain.
University of The Basque Country, The Basque Country, Bizkaia, Spain.
Rheumatology (Oxford). 2024 Feb 6;63(SI):SI96-SI106. doi: 10.1093/rheumatology/kead538.
In this review, we discuss the current evidence on classic and newer oral anticoagulant therapy, older drugs such as HCQ and statins, and new potential treatment targets in APS. Vitamin K antagonists (VKAs) remain the cornerstone treatment for thrombotic events in APS. In patients fulfilling criteria for definite APS presenting with a first venous thrombosis, treatment with VKAs with a target international normalized ratio (INR) 2.0-3.0 is recommended. In patients with arterial thrombosis, treatment with VKA with target INR 2.0-3.0 or 3.0-4.0 is recommended by recent guidelines, considering the individual's bleeding and thrombosis recurrence risk. A combination of VKAs and low-dose aspirin (75-100 mg/daily) may also be considered. According to available evidence direct oral anticoagulants should be avoided in patients with arterial thrombosis and/or those with triple aPL positivity. Adjunctive treatment with HCQ and/or statins can be considered, especially in anticoagulation treatment-refractory APS. Potential targeted treatments in APS include B-cell targeting, complement inhibition, mammalian target of rapamycin inhibition, IFN targeting, adenosine receptors agonists, CD38 targeting or chimeric antigen receptor T-cell therapy. The safety and efficacy of these treatment targets needs to be examined in well-designed randomized controlled trials.
在这篇综述中,我们讨论了经典和新型口服抗凝治疗、羟氯喹和他汀类药物等较老药物以及 APS 中新的潜在治疗靶点的现有证据。维生素 K 拮抗剂 (VKA) 仍然是 APS 血栓事件的基石治疗方法。对于符合明确 APS 标准且首次发生静脉血栓形成的患者,建议使用 VKA 治疗,目标国际标准化比值 (INR) 为 2.0-3.0。根据最近的指南,对于动脉血栓形成的患者,建议使用 VKA 治疗,目标 INR 为 2.0-3.0 或 3.0-4.0,同时考虑到个体的出血和血栓复发风险。也可以考虑 VKA 联合低剂量阿司匹林(75-100mg/天)。根据现有证据,直接口服抗凝剂不应在动脉血栓形成和/或三阳性 aPL 的患者中使用。可以考虑辅助使用羟氯喹和/或他汀类药物,尤其是在抗凝治疗抵抗的 APS 中。APS 中的潜在靶向治疗包括 B 细胞靶向、补体抑制、雷帕霉素靶蛋白抑制、IFN 靶向、腺苷受体激动剂、CD38 靶向或嵌合抗原受体 T 细胞治疗。这些治疗靶点的安全性和疗效需要在精心设计的随机对照试验中进行检查。