Department of Neurology, Johann Wolfgang Goethe-University, Schleusenweg 2-16, 60528, Frankfurt am Main, Germany.
Transl Stroke Res. 2010 Dec;1(4):246-51. doi: 10.1007/s12975-010-0040-6. Epub 2010 Aug 28.
The time span from symptom onset to treatment initiation remains a critical variable determining the efficacy of thrombolysis in acute ischemic stroke. To date, performing a brain scan is indispensable prior to therapy in order to differentiate between patients with ischemic stroke and those with intracerebral hemorrhage (ICH). This causes substantial treatment delay, as thrombolysis cannot be applied prior to hospital admission at much earlier time points. Recently, brain-specific astroglial proteins (i.e., glial fibrillary acidic protein (GFAP), S100B) were identified to be released rapidly from the cytoplasm of destroyed cells in case of acute ICH. Elevated serum concentrations were found within the first 6 h after ICH onset. In contrast, in ischemic stroke, these proteins are released with delay, mirroring the more gradual occurrence of necrotic cell death and blood brain barrier disruption. S100B and GFAP may qualify as candidate serum biomarkers which are able to differentiate between ischemic stroke and ICH in the emergency phase of stroke. This minireview enlightens the pathophysiological background of this finding and provides an overview on currently available clinical data.
从症状发作到开始治疗的时间跨度仍然是决定急性缺血性脑卒中溶栓疗效的关键变量。迄今为止,在进行治疗之前,必须进行脑部扫描,以区分缺血性卒中和脑出血(ICH)患者。这会导致治疗的显著延迟,因为在更早的时间点,在入院之前不能进行溶栓。最近,人们发现脑特异性星形胶质细胞蛋白(即神经胶质纤维酸性蛋白(GFAP)、S100B)在急性 ICH 情况下会从被破坏的细胞的细胞质中迅速释放。ICH 发作后 6 小时内即可发现血清浓度升高。相比之下,在缺血性卒中中,这些蛋白的释放会延迟,反映出坏死性细胞死亡和血脑屏障破坏的发生更为渐进。S100B 和 GFAP 可作为候选血清生物标志物,在卒中的紧急阶段能够区分缺血性卒中和 ICH。这篇综述阐述了这一发现的病理生理学背景,并提供了目前可用的临床数据概述。