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脑缺血中的神经保护:聚焦圣徒试验

Neuroprotection in cerebral ischemia: emphasis on the SAINT trial.

作者信息

Chacon Marcus R, Jensen Matt B, Sattin Justin A, Zivin Justin A

机构信息

Department of Neurosciences, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0624, USA.

出版信息

Curr Cardiol Rep. 2008 Feb;10(1):37-42. doi: 10.1007/s11886-008-0008-2.

Abstract

Acute ischemic stroke (AIS) is a significant cause of death and disability in the United States. It has been 10 years since tissue plasminogen activator became the first medication approved by the US Food and Drug Administration for treatment for AIS. However, this treatment simply reopens arteries. The identification of deleterious cellular reactions that occur secondary to cerebral ischemia has led investigators to search for neuroprotection strategies to complement reperfusion. More than 100 human trials, including a handful of phase III trials, had failed to produce an efficacious neuroprotective agent. In 2006, the first positive trial of neuroprotection was published: the SAINT I (Stroke-Acute Ischemic NXY Treatment) study. In February 2008, the SAINT II study was published, indicating that NXY-059 was not effective for AIS treatment.

摘要

急性缺血性中风(AIS)是美国死亡和残疾的一个重要原因。自组织型纤溶酶原激活剂成为美国食品药品监督管理局批准用于治疗AIS的首个药物以来,已经过去了10年。然而,这种治疗仅仅是重新开通动脉。对脑缺血继发的有害细胞反应的识别促使研究人员寻找神经保护策略以补充再灌注治疗。100多项人体试验,包括少数III期试验,均未能产生一种有效的神经保护剂。2006年,首个神经保护阳性试验发表:SAINT I(中风-急性缺血性NXY治疗)研究。2008年2月,SAINT II研究发表,表明NXY-059对AIS治疗无效。

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