Department of Medicine (Neurology), Duke University School of Medicine, Durham, North Carolina 27710, USA.
Neurotherapeutics. 2010 Jan;7(1):62-73. doi: 10.1016/j.nurt.2009.11.003.
Traumatic brain injury (TBI) is a common cause of long-term neurological morbidity, with devastating personal and societal consequences. At present, no pharmacological intervention clearly improves outcomes, and therefore a compelling unmet clinical need remains. 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors, or "statins," offer a potential novel therapeutic strategy for TBI. Statins are well tolerated, easy to administer, and have a long clinical track record in critically ill patients. Their side effects are well defined and easily monitored. Preclinical studies have shown significant benefit of statins in models of TBI and related disease processes, including cerebral ischemia, intracerebral hemorrhage, and subarachnoid hemorrhage. In fact, multiple mechanisms have been defined by which statins may exert benefit after acute brain injury. Statins are currently positioned to be translated into clinical trials in acute brain injury and have the potential to improve outcomes after TBI.
创伤性脑损伤(TBI)是长期神经功能障碍的常见原因,给个人和社会带来了灾难性的后果。目前,没有明确的药物干预可以改善治疗效果,因此仍然存在迫切的未满足的临床需求。3-羟基-3-甲基戊二酰辅酶 A 还原酶抑制剂,即“他汀类药物”,为 TBI 提供了一种潜在的新的治疗策略。他汀类药物耐受性良好,易于给药,在危重病患者中有长期的临床记录。它们的副作用定义明确,易于监测。临床前研究表明,他汀类药物在 TBI 及相关疾病过程的模型中具有显著的益处,包括脑缺血、脑出血和蛛网膜下腔出血。事实上,已经确定了他汀类药物在急性脑损伤后发挥作用的多种机制。他汀类药物目前有望在急性脑损伤的临床试验中转化,并有可能改善 TBI 后的治疗效果。