Department of Neurology, The Second Affiliated Hospital of Nantong University, Nantong, China.
Department of Neurology, The Second Affiliated Hospital of Nantong University, Nantong, China.
J Stroke Cerebrovasc Dis. 2020 Aug;29(8):104991. doi: 10.1016/j.jstrokecerebrovasdis.2020.104991. Epub 2020 Jun 12.
Fibrinogen is a central protein of hemostasis and a major determinant of plasma viscosity and key factor for platelet activation. The aim of this study is to investigate the relationship between fibrinogen level and short-term outcome in acute ischemic stroke patients receiving intravenous thrombolysis.
This retrospective study included 176 acute ischemic stroke patients who received intravenous thrombolysis with recombinant tissue plasminogen activator and provided plasma fibrinogen level within 24 h after stroke onset. Patients were categorized by plasma fibrinogen level: Quartile 1 (≤ 1.74 g/L), Quartile 2 (1.75-2.08 g/L), Quartile 3 (2.09-2.69 g/L), and Quartile 4 (> 2.69 g/L). The medical record of each patient was reviewed, and demographic, clinical and laboratory information was abstracted. Functional outcome at 14 days was assessed with the modified Rankin Scale.
Poor outcome was present in 75 (42.6%) of the 176 patients that were included in the study (mean age, 72 years; male, 53.4%). After adjustment for potential confounding variables, higher plasma fibrinogen level on admission was associated with poor outcome (adjusted odds ratio 10.45, 95% confidence interval 1.49-73.15 for Q4:Q1; P = 0.02). According to receiver operating characteristic analysis, the best discriminating factor for poor outcome was a plasma fibrinogen level ≥ 2.585 g/L (area under the curve 0.672; sensitivity 50.7%; specificity 86.1%).
Elevated plasma fibrinogen levels on admission are significantly associated with poor outcome after admission for acute ischemic stroke, suggesting the potential role of plasma fibrinogen level as a predictive marker for short-term poor outcome in acute ischemic stroke patients receiving thrombolytic therapy.
纤维蛋白原是止血的核心蛋白,也是血浆粘度的主要决定因素和血小板激活的关键因素。本研究旨在探讨急性缺血性脑卒中患者接受静脉溶栓治疗后纤维蛋白原水平与短期预后的关系。
本回顾性研究纳入了 176 例接受重组组织型纤溶酶原激活物静脉溶栓治疗的急性缺血性脑卒中患者,并在发病后 24 小时内提供了血浆纤维蛋白原水平。根据血浆纤维蛋白原水平将患者分为 4 个四分位组:第 1 四分位组(≤1.74g/L)、第 2 四分位组(1.75-2.08g/L)、第 3 四分位组(2.09-2.69g/L)和第 4 四分位组(>2.69g/L)。回顾了每位患者的病历,提取了人口统计学、临床和实验室信息。使用改良 Rankin 量表评估 14 天的功能结局。
在纳入本研究的 176 例患者中,75 例(42.6%)预后不良(平均年龄 72 岁,男性占 53.4%)。在校正潜在混杂因素后,入院时较高的血浆纤维蛋白原水平与不良预后相关(调整后优势比 10.45,95%置信区间 1.49-73.15,四分位 4:四分位 1;P=0.02)。根据受试者工作特征分析,预测不良预后的最佳区分因素是血浆纤维蛋白原水平≥2.585g/L(曲线下面积 0.672;敏感性 50.7%;特异性 86.1%)。
急性缺血性脑卒中患者入院时的血浆纤维蛋白原水平升高与入院后不良预后显著相关,提示血浆纤维蛋白原水平作为接受溶栓治疗的急性缺血性脑卒中患者短期不良预后的预测标志物具有潜在作用。