Pham Andrew T, Peterson Ryan A, Slaughter Suzanne, Martin Morgan, Hippensteel Joseph A, Burnham Ellen L
Division of General Internal Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.
Department of Biostatistics and Informatics, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.
CHEST Crit Care. 2025 Jun;3(2). doi: 10.1016/j.chstcc.2025.100143. Epub 2025 Mar 3.
Delirium commonly occurs in critical illness and is associated with significant morbidity and mortality. Although risk reduction measures can mitigate the risk of delirium, identifying patients in whom delirium will develop remains clinically challenging.
In critically ill patients with respiratory failure, are central nervous system (CNS)-related biomarkers measured at admission associated with delirium diagnosis?
We performed a secondary analysis of a cohort of patients with respiratory failure in the medical ICU enrolled at a single medical center. Using serum collected at ICU admission, we measured CNS-related biomarkers including brain-derived neurotrophic factor (BDNF), chitinase-3-like protein 1, glial fibrillary acidic protein, neurofilament light chain (NF-L), neurogranin, S100 calcium-binding protein B, and triggering receptor expressed on myeloid cells 2 via a multiplex immunoassay. The primary outcome was diagnosis of in-hospital delirium, defined using validated methods. Associations between individual biomarkers and delirium diagnosis were examined using multivariable logistic regressions, adjusting for factors known to predispose and precipitate delirium. Secondary outcomes included in-hospital mortality, ventilator-free days, ICU-free days, and hospital-free days.
Serum biomarkers were measured in 100 patients. Delirium occurred in 73% of the cohort. Patients with vs without delirium did not differ significantly in terms of age, sex, comorbidities, severity of illness, or unhealthy alcohol use. After adjustment, NF-L was associated positively with delirium diagnosis (adjusted OR, 1.86; 95% CI, 1.09-3.43), whereas BDNF was associated negatively with delirium (adjusted OR, 0.43; 95% CI, 0.15-0.82). No associations were found between other measured biomarkers and delirium diagnosis. NF-L levels were associated negatively with ICU-free and hospital-free days.
Our results indicate that CNS-related biomarkers measured at ICU admission are associated with delirium diagnosis in critically ill patients. Prospective investigations are necessary to validate the role of these biomarkers in predicting delirium.
谵妄在危重症中常见,且与显著的发病率和死亡率相关。尽管降低风险措施可减轻谵妄风险,但识别将发生谵妄的患者在临床上仍具有挑战性。
在呼吸衰竭的危重症患者中,入院时测量的中枢神经系统(CNS)相关生物标志物与谵妄诊断是否相关?
我们对在单一医疗中心入组的内科重症监护病房(ICU)呼吸衰竭患者队列进行了二次分析。使用ICU入院时采集的血清,我们通过多重免疫测定法测量了CNS相关生物标志物,包括脑源性神经营养因子(BDNF)、几丁质酶3样蛋白1、胶质纤维酸性蛋白、神经丝轻链(NF-L)、神经颗粒素、S100钙结合蛋白B以及髓样细胞表达的触发受体2。主要结局是使用经过验证的方法定义的院内谵妄诊断。使用多变量逻辑回归分析个体生物标志物与谵妄诊断之间的关联,并对已知易患和促发谵妄的因素进行校正。次要结局包括院内死亡率、无呼吸机天数、无ICU天数和无住院天数。
对100例患者测量了血清生物标志物。该队列中73%的患者发生了谵妄。发生谵妄与未发生谵妄的患者在年龄、性别、合并症、疾病严重程度或不健康饮酒方面无显著差异。校正后,NF-L与谵妄诊断呈正相关(校正比值比[OR],1.86;95%置信区间[CI],1.09 - 3.43),而BDNF与谵妄呈负相关(校正OR,0.43;95% CI,0.15 - 0.82)。在其他测量的生物标志物与谵妄诊断之间未发现关联。NF-L水平与无ICU天数和无住院天数呈负相关。
我们的结果表明,ICU入院时测量的CNS相关生物标志物与危重症患者的谵妄诊断相关。有必要进行前瞻性研究以验证这些生物标志物在预测谵妄中的作用。