Department of Biomedical Sciences, Humanitas University, Milan, Italy.
Department of Gastroenterology and Inserm NGERE U1256, University Hospital of Nancy, University of Lorraine, Vandoeuvre-lès-Nancy, France.
Curr Drug Targets. 2021;22(1):126-136. doi: 10.2174/1389450121666200902164240.
Patients with inflammatory bowel diseases (IBD) have an increased risk of thrombosis. The interaction between inflammation and coagulation has extensively been studied. It is well-- known that some drugs can influence the haemostatic system, but several concerns on the association between therapies and increased risk of thrombosis remain open. While biologics seem to have a protective role against thrombosis via their anti-inflammatory effect, some concerns about an increased risk of thrombosis with JAK inhibitors have been raised. We conducted a literature review to assess the association between biologics/small molecules and venous/arterial thrombotic complications. An increased risk of venous and arterial thrombosis was found in patients treated with corticosteroids, whereas anti-TNFα were considered protective agents. No thromboembolic adverse event was reported with vedolizumab and ustekinumab. In addition, thromboembolic events rarely occurred in patients with ulcerative colitis (UC) after therapy with tofacitinib. The overall risk of both venous and arterial thrombosis was not increased based on the available evidence. Finally, in the era of JAK inhibitors, the treatment should be individualized by evaluating the pre-existing potential thrombotic risk balanced with the intrinsic risk of the medication used.
炎症性肠病(IBD)患者有血栓形成的风险增加。炎症与凝血之间的相互作用已经得到了广泛的研究。众所周知,一些药物会影响止血系统,但关于治疗与血栓形成风险增加之间的关联仍存在一些问题。虽然生物制剂通过其抗炎作用似乎对血栓形成有保护作用,但有人担心 JAK 抑制剂会增加血栓形成的风险。我们进行了文献回顾,以评估生物制剂/小分子与静脉/动脉血栓并发症之间的关系。发现接受皮质类固醇治疗的患者静脉和动脉血栓形成的风险增加,而抗 TNFα 被认为是保护剂。vedolizumab 和 ustekinumab 未报告血栓栓塞不良事件。此外,在接受 tofacitinib 治疗后,溃疡性结肠炎(UC)患者很少发生血栓栓塞事件。根据现有证据,静脉和动脉血栓形成的总体风险并未增加。最后,在 JAK 抑制剂时代,应通过评估潜在的血栓形成风险与所使用药物的固有风险来个体化治疗。