Texas Tech. University Health Sciences Center, 3601 4th St Stop 9410, Lubbock, TX, 79430-9410, USA.
Department of Internal Medicine, Texas Tech. University Health Sciences Center, 3601 4th St Stop 9410, Lubbock, TX, 79430-9410, USA.
J Thromb Thrombolysis. 2018 May;45(4):516-528. doi: 10.1007/s11239-018-1623-4.
Thrombosis is common in cancer patients and is associated with increased morbidity and mortality. Myeloproliferative neoplasms (MPN) are common malignancies in elderly individuals and are known for a high incidence of thrombotic complications. Different risk factors have been identified in studies, and risk models have been developed to identify patients with MPN at higher risk for thrombosis. Several pathophysiological mechanisms help explain the increased likelihood of thrombosis in these patients. Factors, such as leukocyte and platelet activation leading to the formation of leukocyte-platelet aggregates, activation of the coagulation cascade by microparticles, high levels of inflammatory cytokines, and endothelial dysfunction have a crucial role in thrombosis in MPN patients. Recent studies have demonstrated a significant association between the allele burden of specific genetic mutations (mainly JAK2V617F) associated with MPN and the incidence of thrombotic events, thus suggesting a possible role for these mutations in thrombogenesis.
血栓形成在癌症患者中很常见,与发病率和死亡率的增加有关。骨髓增殖性肿瘤(MPN)是老年人常见的恶性肿瘤,其血栓并发症的发生率很高。在研究中已经确定了不同的危险因素,并开发了风险模型来识别 MPN 患者中血栓形成风险较高的患者。一些病理生理机制有助于解释这些患者血栓形成的可能性增加。白细胞和血小板激活导致白细胞-血小板聚集形成、微颗粒激活凝血级联反应、炎症细胞因子水平升高和内皮功能障碍等因素在 MPN 患者的血栓形成中起着关键作用。最近的研究表明,与 MPN 相关的特定基因突变(主要是 JAK2V617F)的等位基因负担与血栓形成事件的发生率之间存在显著关联,因此这些突变可能在血栓形成中起作用。