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Inflammatory Response in the First 48 Hours of Acute Ischemic Stroke

机译:急性缺血性中风前48小时的炎症反应

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Background: Activation of endothelial cells is an important mediator of atherothrombosis. Markers of endothelial cells such as soluble adhesion molecules can be measured in plasma and reflect the activity of the endothelium and the inflammatory system. We hypothesized that patients with acute ischemic stroke would have a dynamic change in their markers of inflammation over time, primarily reflecting the activation of endothelial cells and the immunological ability to respond to an acute brain insult. We also believed that the acute inflammatory response in the first 72 hours might affect the short and long term clinical outcome.Methods: We conducted a prospective case study of 27 patients that were admitted with acute ischemic stroke during the years 2005 - 2007. All were examined clinically using the National Institute of Health Stroke Scale [NIHSS] and a brain computed tomography (CT) scan was done in the first 24 hours. Blood was drawn for levels of E-selectin, intracellular adhesion molecule 1 (ICAM-1), and vascular cellular adhesion molecule 1 (VCAM-1) on admission and 48 hours later by ELISA methods. The blood was separated and the serum was frozen at -80 °C until analyzed as one batch. Results: Mean blood concentrations of soluble E-selectin, intracellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) were measured on admission and 48 hours later. Clinically there were 3 groups: 6 patients with transient ischemic attack [TIA] (58 ± 12 years old, 3 women and 3 men), 8 patients with cerebrovascular accident [CVA] without recovery (75 ± 18 years old, 4 women and 4 men), and 13 patients with CVA who recovered clinically (70 ± 13 years old, 6 women and 7 men). There was a significant increase in E-selectin levels in the second measurement (from 27.5 ± 21.6 ng/ml to 38.7 ± 19.6 ng/ml; Z = -1.997, P = 0.046) in the TIA group. An inverse correlation was found between E-selectin level and age among TIA patients on admission (r = -0.913, P = 0.011) and 48 hours later (r = -0.850, P = 0.032). A positive correlation between ICAM-1 and VCAM-1 levels was found 48 hours post admission (r = 0.436, P = 0.026).Conclusions: We have demonstrated a significant increase in E-selectin level within 48 hours among patients with TIA. In the TIA group there was an inverse correlation between age and E-selectin level. This may suggest that younger patients can protect their ischemic brain more efficiently due to a more competent immune system, and that the immune system may have an important role in ischemic brain injury.doi:10.4021/jnr101e
机译:背景:内皮细胞的激活是动脉粥样硬化的重要介质。可以在血浆中测量内皮细胞的标记物,例如可溶性粘附分子,并反映内皮细胞和炎症系统的活性。我们假设急性缺血性中风患者的炎症标志会随着时间而动态变化,这主要反映了内皮细胞的激活和对急性脑损伤的免疫能力。我们还认为,前72小时的急性炎症反应可能会影响短期和长期的临床结果。方法:我们对2005年至2007年期间收治的27例急性缺血性卒中患者进行了前瞻性病例研究。使用国立卫生研究院卒中量表[NIHSS]对患者进行了临床检查,并在头24小时内进行了计算机断层扫描(CT)扫描。在入院时和48小时后通过ELISA方法抽取血液中的E-选择蛋白,细胞内粘附分子1(ICAM-1)和血管细胞粘附分子1(VCAM-1)的水平。分离血液,将血清冷冻在-80℃,直到分批分析。结果:入院时和入院后48小时测量了可溶性E-选择素,细胞内粘附分子1(ICAM-1)和血管细胞粘附分子1(VCAM-1)的平均血药浓度。临床上分为3组:6例短暂性脑缺血发作[TIA]患者(58±12岁,3名女性和3名男性),8例脑血管意外[CVA]患者无恢复(75±18岁,4名女性和4名)男性)和13例临床恢复的CVA患者(70±13岁,6名女性和7名男性)。在TIA组中,第二次测量中E-选择素水平显着增加(从27.5±21.6 ng / ml增至38.7±19.6 ng / ml; Z = -1.997,P = 0.046)。发现TIA患者入院时E-选择素水平与年龄呈负相关(r = -0.913,P = 0.011)和48小时后(r = -0.850,P = 0.032)。入院48小时后发现ICAM-1和VCAM-1水平呈正相关(r = 0.436,P = 0.026)。结论:我们已经证明TIA患者48小时内E-选择素水平显着增加。在TIA组中,年龄与E-选择素水平呈负相关。这可能表明年轻的患者由于免疫系统功能更强而可以更有效地保护缺血性脑,并且免疫系统可能在缺血性脑损伤中起重要作用。doi:10.4021 / jnr101e

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