Pfeilschifter Waltraud, Steinstraesser Thurid, Paulus Patrick, Zeiner Pia Susan, Bohmann Ferdinand, Theisen Alf, Lindhoff-Last Edelgard, Penski Cornelia, Wagner Marlies, Mittelbronn Michel, Foerch Christian
1 Department of Neurology, Goethe-University, Frankfurt am Main, Germany.
2 Department of Anesthesiology and Operative Intensive Care Medicine, Kepler University Hospital, Linz, Austria.
J Cereb Blood Flow Metab. 2017 Mar;37(3):855-865. doi: 10.1177/0271678X16642443. Epub 2016 Jul 20.
New oral anticoagulants for the prevention of stroke and systemic embolism in patients with atrial fibrillation have recently been introduced. In this translational study, we explored the risk of long-term anticoagulation on intracerebral hemorrhage under sustained severe arterial hypertension. We initiated anticoagulation with warfarin or apixaban in spontaneously hypertensive rats prone to develop severe hypertension and subsequent intracerebral bleeding complications. A non-anticoagulated group served as control. During an 11-week-study period, blood pressure, anticoagulation parameters, and clinical status were determined regularly. The incidence of histopathologically proven intracerebral hemorrhage was defined as the primary endpoint. Both warfarin and apixaban anticoagulation was fairly stable during the study period, and all rats developed severe hypertension. Intracerebral hemorrhage was determined in 29% (4/14) of warfarin rats and in 10% (1/10) of apixaban rats. Controls did not show cerebral bleeding complications (chi-square not significant). Mortality rate at study termination was 33% (2/6) in controls, 43% (6/14) in the warfarin group, and 60% (6/10) in the apixaban group. Animals died from extracerebral complications in most cases. Our study describes an experimental intracerebral hemorrhage model in the context of sustained hypertension and long-term anticoagulation. Extracerebral bleeding complications occurred more often in warfarin-treated animals compared with apixaban and control rats.
近期已推出用于预防心房颤动患者中风和全身性栓塞的新型口服抗凝剂。在这项转化研究中,我们探讨了在持续性重度动脉高血压情况下长期抗凝治疗引发脑出血的风险。我们对易发生重度高血压及后续脑出血并发症的自发性高血压大鼠启动华法林或阿哌沙班抗凝治疗。一个未进行抗凝治疗的组作为对照。在为期11周的研究期间,定期测定血压、抗凝参数和临床状态。组织病理学证实的脑出血发生率被定义为主要终点。在研究期间,华法林和阿哌沙班的抗凝效果均相当稳定,且所有大鼠均出现了重度高血压。华法林组大鼠中有29%(4/14)发生脑出血,阿哌沙班组大鼠中有10%(1/10)发生脑出血。对照组未出现脑出血并发症(卡方检验无显著性差异)。研究结束时,对照组的死亡率为33%(2/6),华法林组为43%(6/14),阿哌沙班组为60%(6/10)。大多数情况下,动物死于脑外并发症。我们的研究描述了一种在持续性高血压和长期抗凝背景下的实验性脑出血模型。与阿哌沙班组和对照组大鼠相比,接受华法林治疗的动物发生脑外出血并发症的情况更为常见。