Diagnostic Value of S100B and Neuron-specific Enolase in Distinguishing Acute Central and Peripheral Vertigo

IF 0.3 Q4 EMERGENCY MEDICINE Eurasian Journal of Emergency Medicine Pub Date : 2022-12-09 DOI:10.4274/eajem.galenos.2022.82687
B. Masoumi, Razieh Bagheri, Farhad Heydari, Abaris Massoumi, B. Ansari, Mohammad Nasr-Esfahani
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Abstract

Aim: Vertigo is a common presenting complaint to the emergency department (ED). Distinguishing between acute central and peripheral vertigo can be challenging. During recent years, several biomarkers have been introduced for use in distinguishing central and peripheral vertigo. The current study determined whether S100 calcium-binding protein B (S100B) and neuron-specific enolase (NSE) serum concentrations could effectively predict the central causes of vertigo. Materials and Methods: This was a prospective study performed on 117 patients with acute vertigo who were admitted to the ED. All patients underwent magnetic resonance imaging (MRI) and the results of the MRI were considered the gold standard. S100B and NSE from blood samples taken <8 h after the onset of symptoms were measured in all patients. Results: Finally, 117 patients were enrolled in the study, of which 43 patients had central vertigo and 74 patients had peripheral vertigo. The serum levels of S100B and NSE in the central group were significantly higher (60.62 vs 28.01 pg/mL, and 11.86 vs 7 ng/mL, p<0.001, respectively). The receiver-operating characteristic analysis demonstrated an AUC of 0.91 [95% confidence interval (CI): 0.84-0.96] and 0.93 (95% CI: 0.87-0.97) for S100B and NSE for predicting central vertigo and reported a sensitivity of 97.7% and 93% and a specificity of 87.8% and 89.2% for detecting the central cause of vertigo with S100B and NSE. Conclusion: The serum S100B and NSE concentrations in central vertigo were significantly higher, and could be useful markers in screening central from peripheral vertigo in the ED.
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S100B和神经元特异性烯醇化酶对急性中枢性和外周性眩晕的诊断价值
目的:眩晕是向急诊科(ED)提出的常见投诉。区分急性中枢性眩晕和周围性眩晕可能具有挑战性。近年来,一些生物标志物被引入用于区分中枢性眩晕和周围性眩晕。目前的研究确定了S100钙结合蛋白B(S100B)和神经元特异性烯醇化酶(NSE)血清浓度是否能有效预测眩晕的中心原因。材料和方法:这是一项前瞻性研究,对117名急诊科急性眩晕患者进行了研究。所有患者都接受了磁共振成像(MRI),MRI结果被认为是金标准。在所有患者中测量症状出现后<8h采集的血样中的S100B和NSE。结果:共有117例患者参与研究,其中43例为中心性眩晕,74例为周围性眩晕。中心组的血清S100B和NSE水平显著升高(分别为60.62和28.01 pg/mL,11.86和7 ng/mL,p<0.001)。受试者操作特征分析显示,S100B和NSE预测中枢性眩晕的AUC分别为0.91[95%置信区间(CI):0.84-0.96]和0.93(95%CI:0.87-0.97),并报告了S100B和NSE检测眩晕中枢原因的敏感性为97.7%和93%,特异性为87.8%和89.2%。结论:中枢性眩晕患者血清S100B和NSE浓度明显增高,可作为ED患者中枢性眩晕和周围性眩晕的筛查指标。
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来源期刊
自引率
50.00%
发文量
39
审稿时长
10 weeks
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