Department of Neurology, Hospital Clínico Universitario, Universidad de Santiago de Compostela, Santiago de Compostela, Spain.
Thromb Haemost. 2011 Mar;105(3):421-9. doi: 10.1160/TH10-09-0621. Epub 2010 Dec 21.
Neuroserpin is a brain-derived natural inhibitor of tissue plasminogen activator (tPA) that has shown neuroprotective effects in animal models of brain ischaemia. Our aim was to investigate the association of neuroserpin levels in blood with functional outcome in patients with acute ischaemic stroke. Due to the potential effect of tPA treatment interfering on neuroserpin levels, we studied two different cohorts: 129 patients not treated with tPA and 80 patients treated with intravenous tPA within 3 hours (h) from symptoms onset. Neuroserpin levels were measured by ELISA. Good functional outcome at three months was defined as Rankin scale score ≤2. In the two cohorts, serum neuroserpin levels on admission were significantly higher than at 24 h, 72 h and in healthy subjects. In non tPA-treated patients, neuroserpin levels decrease at 24 h, but not levels at baseline, were associated with good outcome (for each quartile decrease, adjusted odds ratio [OR] 15.0; 95% confidence interval [CI], 3.5 to 66). In the tPA-treated cohort, high neuroserpin levels before tPA bolus had the stronger effect on favourable outcome (for each quartile, OR 13.5; 95%CI, 3.9 to 47). Furthermore, for each quartile in neuroserpin levels before tPA bolus there was a 80% (95%CI, 48 to 92) reduction in the probability of subsequent parenchymal haematoma. In summary, high serum neuroserpin levels before intravenous tPA and neuroserpin levels decrease at 24 h after ischaemic stroke, independently of tPA treatment, are associated with good functional outcome. These findings support the concept that neuroserpin might play an important role during cerebral ischaemia.
神经丝氨酸蛋白酶抑制剂是一种脑源性组织型纤溶酶原激活物(tPA)的天然抑制剂,在脑缺血动物模型中显示出神经保护作用。我们的目的是研究血液中神经丝氨酸蛋白酶抑制剂水平与急性缺血性脑卒中患者功能结局的关系。由于 tPA 治疗可能会干扰神经丝氨酸蛋白酶抑制剂水平,因此我们研究了两个不同的队列:129 例未接受 tPA 治疗的患者和 80 例症状发作后 3 小时内接受静脉 tPA 治疗的患者。通过 ELISA 法测量神经丝氨酸蛋白酶抑制剂水平。3 个月时功能结局良好定义为 Rankin 量表评分≤2。在两个队列中,入院时血清神经丝氨酸蛋白酶抑制剂水平明显高于 24 小时、72 小时和健康受试者。在未接受 tPA 治疗的患者中,神经丝氨酸蛋白酶抑制剂水平在 24 小时下降,但与基线相比,神经丝氨酸蛋白酶抑制剂水平下降与良好结局相关(每下降一个四分位间距,调整后的优势比 [OR] 15.0;95%置信区间 [CI],3.5 至 66)。在接受 tPA 治疗的队列中,tPA 推注前的高神经丝氨酸蛋白酶抑制剂水平对有利结局的影响更强(每下降一个四分位间距,OR 13.5;95%CI,3.9 至 47)。此外,在 tPA 推注前神经丝氨酸蛋白酶抑制剂水平的每个四分位间距内,随后发生实质血肿的概率降低了 80%(95%CI,48 至 92)。总之,静脉 tPA 前血清神经丝氨酸蛋白酶抑制剂水平高和缺血性脑卒中后 24 小时神经丝氨酸蛋白酶抑制剂水平下降,独立于 tPA 治疗,与良好的功能结局相关。这些发现支持神经丝氨酸蛋白酶抑制剂在脑缺血期间可能发挥重要作用的概念。