Neuron-specific enolase and Tau protein as biomarkers for sepsis-associated delirium: a cross-sectional pilot study.

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL
Einstein-Sao Paulo Pub Date : 2025-04-07 eCollection Date: 2025-01-01 DOI:10.31744/einstein_journal/2025AO1244
Agnes Araújo Sardinha Pinto, Maira Mello de Carvalho, Juliana Bahia Santos, Rebeca Souza da Silva, Hermes Vieira Barbeiro, Luz Marina Gómez Gómez, Ian Ward Abdalla Maia, Júlio Flávio Meirelles Marchini, Flávia Barreto Garcez, Thiago Junqueira Avelino-Silva, Lucas de Moraes Soler, Matheus Menão Mochetti, Heraldo Possolo de Souza, Júlio Cesar Garcia Alencar
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引用次数: 0

Abstract

Background: In this study, Pinto et al. identified significantly higher levels of neuron-specific enolase and Tau protein in older patients with sepsis-associated delirium in the emergency department, suggesting the potential of these biomarkers as diagnostic tools in this population.

Objective: Sepsis-associated delirium is a common cerebral manifestation in patients with sepsis, potentially caused by a combination of neuroinflammation and other neurophysiological disorders. This study investigated the expression of neuron-specific enolase and Tau protein as biomarkers in patients with sepsis-associated delirium. While neuron-specific enolase and Tau protein are known to be associated with brain injury, their diagnostic potential in patients with sepsis-associated delirium is not well understood.

Methods: This cross-sectional pilot study evaluated plasma levels of neuron-specific enolase and Tau protein in patients with delirium and sepsis to explore their potential for identifying sepsis in patients admitted to the emergency department.

Results: A total of 25 patients with delirium were analyzed, 56% of whom had sepsis. Patients with sepsis exhibited significantly higher neuron-specific enolase levels (2.7ng/mL [95%CI= 2.2-3.2] versus 1.3 ng/mL [95%CI= 0.8-2.5], p<0.003) and Tau protein levels (96.1pg/mL [95%CI= 77.0-111.3] versus 43.0pg/mL [95%CI= 31.2-84.5], p<0.003) compared to patients without sepsis. Neuron-specific enolase and Tau protein thresholds of >2.08ng/mL and >59.27pg/mL, respectively, demonstrated 90% specificity for identifying sepsis in patients.

Conclusion: Neuron-specific enolase and Tau protein levels were significantly higher in patients with sepsis than in those without, underscoring their potential ability to identify the infectious etiology of delirium in older patients admitted to emergency departments. Clinical Trials #RBR-233bct.

Background: ■ Biomarkers of brain injury, such as neuron-specific enolase and Tau proteins, are higher in older patients with sepsis and delirium.

Background: ■ Diagnosing sepsis in patients with delirium can be challenging.

Background: ■ Early identification of sepsis is key to managing sepsisassociated delirium.

神经元特异性烯醇化酶和Tau蛋白作为败血症相关谵妄的生物标志物:一项横断面先导研究
背景:在这项研究中,Pinto等人发现急诊科患有败血症相关性谵妄的老年患者中神经元特异性烯醇化酶和Tau蛋白水平显著升高,这表明这些生物标志物有可能作为该人群的诊断工具。目的:脓毒症相关性谵妄是脓毒症患者常见的一种脑部表现,可能由神经炎症和其他神经生理障碍共同引起。本研究探讨了神经元特异性烯醇化酶和Tau蛋白作为生物标志物在败血症相关性谵妄患者中的表达。虽然已知神经元特异性烯醇化酶和Tau蛋白与脑损伤有关,但它们在败血症相关性谵妄患者中的诊断潜力尚不清楚。方法:本横断性初步研究评估谵妄和败血症患者的血浆神经元特异性烯醇化酶和Tau蛋白水平,以探讨其在识别急诊患者败血症方面的潜力。结果:共分析25例谵妄患者,其中56%合并脓毒症。脓毒症患者神经元特异性烯醇化酶水平明显高于脓毒症患者(2.7ng/mL [95%CI= 2.2-3.2] vs . 1.3 ng/mL [95%CI= 0.8-2.5], p2.08ng/mL和bb0 59.27pg/mL),对脓毒症患者的特异性为90%。结论:脓毒症患者的神经元特异性烯醇化酶和Tau蛋白水平明显高于非脓毒症患者,强调了它们在识别急诊住院老年患者谵妄感染病因方面的潜在能力。临床试验#RBR-233bct。脑损伤的生物标志物,如神经元特异性烯醇化酶和Tau蛋白,在老年脓毒症和谵妄患者中较高。背景:■诊断谵妄患者的败血症具有挑战性。背景:早期识别败血症是处理败血症相关性谵妄的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Einstein-Sao Paulo
Einstein-Sao Paulo MEDICINE, GENERAL & INTERNAL-
CiteScore
2.00
自引率
0.00%
发文量
210
审稿时长
38 weeks
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