Sheth Kevin N, Simard J Marc, Elm Jordan, Kronenberg Golo, Kunte Hagen, Kimberly W Taylor
Division of Neurocritical Care and Emergency Neurology, Yale University School of Medicine, 15 York Street, LCI 10th Floor, New Haven, CT, 06520, USA.
Department of Neurosurgery, University of Maryland School of Medicine, Baltimore, MD, USA.
Acta Neurochir Suppl. 2016;121:13-8. doi: 10.1007/978-3-319-18497-5_3.
The SUR1-TRPM4 channel is a critical determinant of edema and hemorrhagic transformation after focal ischemia. Blockade of this channel by the small molecule glyburide results in improved survival and neurological outcome in multiple preclinical models of ischemic stroke. A robust, compelling body of evidence suggests that an intravenous formulation of glyburide, RP-1127, can prevent swelling and improve outcome in patients with stroke. Retrospective studies of diabetic stroke patients show improved outcomes in patients who are continued on sulfonylureas after stroke onset. An early phase II study using magnetic resonance imaging and plasma biomarkers supports the conclusion that RP-1127 may decrease swelling and hemorrhagic transformation. Finally, the ongoing phase II RP-1127 development program has demonstrated continued safety as well as feasibility of enrollment and tolerability of the intervention. Continued efforts to complete the ongoing phase II study and definitive efficacy studies are needed to bring a candidate pharmacotherapy to a population of severe stroke patients that currently have no alternative.
SUR1-TRPM4通道是局灶性缺血后水肿和出血转化的关键决定因素。小分子格列本脲对该通道的阻断可改善多种缺血性中风临床前模型的生存率和神经功能结局。大量有力的证据表明,格列本脲的静脉制剂RP-1127可预防中风患者的肿胀并改善其结局。对糖尿病中风患者的回顾性研究表明,中风发作后继续使用磺脲类药物的患者结局有所改善。一项使用磁共振成像和血浆生物标志物的II期早期研究支持了RP-1127可能减少肿胀和出血转化的结论。最后,正在进行的II期RP-1127开发项目已证明其持续安全性以及干预措施的入组可行性和耐受性。需要继续努力完成正在进行的II期研究和确定性疗效研究,以便为目前没有其他选择的严重中风患者群体带来一种候选药物疗法。