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基于一组临床标准的神经标志物对轻度创伤性脑损伤患者的预测价值:试验中的 S100B 蛋白和神经元特异性烯醇化酶:临床文章。

Predictive value of neuromarkers supported by a set of clinical criteria in patients with mild traumatic brain injury: S100B protein and neuron-specific enolase on trial: clinical article.

机构信息

Department of Trauma Surgery, Medical University of Vienna, Vienna, Austria.

出版信息

J Neurosurg. 2013 Jun;118(6):1298-303. doi: 10.3171/2013.1.JNS121181. Epub 2013 Mar 1.

Abstract

OBJECT

The role of the neuromarkers S100B protein and neuron-specific enolase (NSE) in minor head injury is well established. Moreover, there are sensitive decision rules available in the literature to identify clinically important brain lesions. However, it is not clear if using the biomarkers has an influence on the predictability of the decision rule. The purpose of this study was to determine if a set of preclinical and clinical parameters combined with 2 neuromarker levels could serve as reliable guidance for accurate diagnosis.

METHODS

Prospective evaluation of a cohort of head trauma patients with Glasgow Coma Scale scores of 13-15 was performed at an academic, Level I trauma center. Blood samples and cranial CT studies were obtained for all patients within 3 hours after injury. The hypothesis of the study was whether the combination of an increase of S100B and NSE levels in serum and other defined risk factors are associated with a pathological finding on CT. A forward stepwise logistic regression model was used.

RESULTS

The study included 107 head trauma patients with a mean age of 59 ± 23 years. Twenty-five patients (23.4%) had traumatic lesions on CT. Eight patients underwent craniotomy. The analysis provided a model with good overall accuracy for discriminating cases with clinically important brain injury, including the 6 variables of S100B, NSE, nausea, amnesia, vomiting, and loss of consciousness. The area under the curve (AUC) was 0.88 (0.83-0.93). The receiver operating characteristic curve plots detecting clinically important brain injury for the single variables of S100B and NSE showed an AUC of 0.63 and 0.64, respectively. Conclusions The integration of the neuromarker panel as part of a diagnostic rule including the high-risk factors of nausea, vomiting, amnesia, and loss of consciousness is safe and reliable in determining a diagnosis, pending the availability of more brain-specific neuromarkers. CLINICAL TRIAL REGISTRATION NO.: NCT00622778 (ClinicalTrials.gov).

摘要

目的

S100B 蛋白和神经元特异性烯醇化酶(NSE)等神经标志物在轻微头部损伤中的作用已得到充分证实。此外,文献中还提供了敏感的决策规则来识别临床上重要的脑损伤。然而,目前尚不清楚使用这些生物标志物是否会影响决策规则的可预测性。本研究旨在确定一组临床前和临床参数与 2 种神经标志物水平相结合,是否可以作为准确诊断的可靠指导。

方法

在一家学术性一级创伤中心,对格拉斯哥昏迷量表评分为 13-15 的头部创伤患者队列进行前瞻性评估。所有患者在受伤后 3 小时内均进行了血液样本和颅 CT 研究。本研究的假设是,血清中 S100B 和 NSE 水平的升高以及其他确定的危险因素的组合是否与 CT 上的病理性发现相关。使用逐步向前逻辑回归模型。

结果

该研究纳入了 107 例头部创伤患者,平均年龄为 59±23 岁。25 例(23.4%)患者 CT 上有创伤性病变。8 例患者接受了开颅手术。分析结果提供了一个用于区分具有临床重要脑损伤的病例的综合模型,该模型包含 S100B、NSE、恶心、遗忘、呕吐和意识丧失等 6 个变量。该模型的整体准确性较好,曲线下面积(AUC)为 0.88(0.83-0.93)。S100B 和 NSE 等单个变量检测临床重要脑损伤的受试者工作特征曲线(ROC)图显示 AUC 分别为 0.63 和 0.64。结论:将神经标志物组作为包括恶心、呕吐、遗忘和意识丧失等高危因素的诊断规则的一部分进行整合是安全可靠的,在有更多脑特异性神经标志物的情况下可以确定诊断。临床试验注册号:NCT00622778(ClinicalTrials.gov)。

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