首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >Temporal profile and clinical significance of serum neuron-specific enolase and S100 in ischemic and hemorrhagic stroke.
【24h】

Temporal profile and clinical significance of serum neuron-specific enolase and S100 in ischemic and hemorrhagic stroke.

机译:缺血性和出血性中风时血清神经元特异性烯醇化酶和S100的时间变化及其临床意义。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Neuron-specific enolase (NSE) and S100 protein are implicated in several brain injuries, including stroke. Our objective was to analyze the temporal profile and the clinical significance of NSE and S-100 in acute ischemic (IS) and intracerebral hemorrhage (ICH). METHODS: We studied 224 patients with IS and 44 patients with ICH. Computerized tomography (CT) scans were performed to assess infarct volume. Stroke severity was evaluated using the National Institute of Health Stroke Scale (NIHSS), and functional outcome at 3 months with the modified Rankin Scale (mRS). Serum NSE and S100 protein were measured using an electrochemiluminescence-immunoassay. RESULTS: Peak values were found at 72 h for NSE and at 24 h for S100 in IS. For ICH, peak values were found at 24 h for both NSE and S100. At these time intervals S100 and NSE correlated with the NIHSS score and were independently associated with poor outcome. CONCLUSIONS: High serum NSE and S100 are associated with poor outcome in IS, and high serum NSE is associated with poor outcome in ICH. These findings suggest the potential utility of NSE and S100 as prognostic markers for acute stroke.
机译:背景:神经元特异性烯醇化酶(NSE)和S100蛋白与多种脑损伤有关,包括中风。我们的目的是分析NSE和S-100在急性缺血(IS)和脑出血(ICH)中的时间变化及其临床意义。方法:我们研究了224例IS患者和44例ICH患者。进行计算机断层扫描(CT)扫描以评估梗死体积。使用国立卫生研究院卒中量表(NIHSS)评估卒中严重程度,并使用改良的兰金量表(mRS)评估3个月时的功能结局。血清NSE和S100蛋白使用电化学发光免疫测定法测量。结果:在IS中,NSE在72 h和S100在24 h发现了峰值。对于ICH,NSE和S100均在24小时发现峰值。在这些时间间隔,S100和NSE与NIHSS评分相关,并且分别与不良预后相关。结论:高血清NSE和S100与IS不良预后相关,而高血清NSE与ICH预后不良相关。这些发现提示NSE和S100作为急性中风的预后标志物的潜在用途。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号