Department of Neurology and Stroke Center, The First Affiliated Hospital, Jinan University, Guangzhou, China; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Department of Neurology and Stroke Center, The First Affiliated Hospital, Jinan University, Guangzhou, China; Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
J Clin Neurosci. 2019 Nov;69:1-6. doi: 10.1016/j.jocn.2019.08.074. Epub 2019 Sep 11.
Thrombolysis-induced haemorrhagic transformation is the most challenging preventable complication in thrombolytic therapy. This condition is often associated with poor functional outcome and long-term disease burden. Statins, or 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, are controversially suggested to either increase or decrease the odds of better primary outcomes compared to treatment without statins after thrombolysis in patients or animals; statins are thought to act by influencing lipid levels, the inflammatory response, blood brain barrier permeability and cell apoptosis. Statins are the cornerstone of secondary prevention of cardiovascular and cerebrovascular diseases. However, the role of statins in acute phase stroke, and the necessity of their use, remains unclear. Currently, whether statins can increase the risk of haemorrhagic transformation is of great concern for patients treated with tissue plasminogen activator (t-PA). Herein, we thoroughly summarize the recent advances that address whether the administration of statins in ischaemic stroke increases haemorrhagic transformation in patients or animals who received thrombolysis at an early stage and the related mechanisms. This review will provide more clinical and preclinical evidence to address questions regarding the exercise of caution in the use of high dose statins in patients who received thrombolysis and if low dose statins may be beneficial in decreasing thrombolysis-induced haemorrhagic transformation.
溶栓治疗引起的出血性转化是溶栓治疗中最具挑战性的可预防并发症。这种情况通常与不良的功能结局和长期疾病负担有关。他汀类药物,或 3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原酶抑制剂,被认为可以增加或降低与溶栓治疗后不用他汀类药物治疗相比的主要结局的可能性,无论是在患者还是动物中;他汀类药物被认为通过影响脂质水平、炎症反应、血脑屏障通透性和细胞凋亡来发挥作用。他汀类药物是心血管和脑血管疾病二级预防的基石。然而,他汀类药物在急性脑卒中中的作用及其使用的必要性仍不清楚。目前,他汀类药物是否会增加出血性转化的风险,是接受组织型纤溶酶原激活剂(t-PA)治疗的患者非常关注的问题。在此,我们全面总结了最近的进展,这些进展涉及他汀类药物在早期接受溶栓治疗的缺血性脑卒中患者或动物中是否会增加出血性转化,以及相关机制。这篇综述将提供更多的临床和临床前证据,以解决关于在接受溶栓治疗的患者中谨慎使用大剂量他汀类药物的问题,以及低剂量他汀类药物是否可能有助于减少溶栓治疗引起的出血性转化。