医学
抗磷脂综合征
血栓形成
发病机制
心肌梗塞
心脏病学
冲程(发动机)
内科学
内皮功能障碍
疾病
血管疾病
自身免疫性疾病
抗体
免疫学
机械工程
工程类
作者
Michel T. Corban,Alí Duarte‐García,Robert D. McBane,Eric L. Matteson,Lilach O. Lerman,Amir Lerman
标识
DOI:10.1016/j.jacc.2017.02.058
摘要
Antiphospholipid syndrome (APS) is an autoimmune disease characterized by venous thromboembolism, arterial thrombosis, and obstetric morbidities in the setting of persistently positive levels of antiphospholipid antibodies measured on 2 different occasions 12 weeks apart. Patients with APS are at increased risk for accelerated atherosclerosis, myocardial infarction, stroke, and valvular heart disease. Vascular endothelial cell dysfunction mediated by antiphospholipid antibodies and subsequent complement system activation play a cardinal role in APS pathogenesis. Improved understanding of their pathogenic function could help in the risk stratification of patients with APS and provide new molecular therapeutic targets.
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