C.5 神经系统受累的重症儿童炎症特征的改变

SG Buttle, D Martin, L. Foster, K. Woodward, M. Esser
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摘要

背景:儿科重症监护病房(PICU)收治的儿童中,每 4 人中就有 1 人以上因各种原因疑似患有神经炎症。尽管炎症通常是有益的,但不受控制的炎症会导致继发性神经损伤并干扰修复机制。研究方法阿尔伯塔儿童医院启动了一项前瞻性队列研究,以评估入住重症监护病房的儿童的神经炎症情况。在多个预定时间点收集的 48 种细胞因子、趋化因子和生长因子与临床轨迹数据一起进行了分析。已完成对 2022 年 1 月至 2023 年 7 月入院患者的初步探索性分析。结果初步分析包括 53 名患者。脑病(18.9%)、缺氧(17%)和创伤性脑损伤(15.1%)是最常见的入组原因。与其他亚组相比,原发性脑部炎症性疾病患者在入院时和第一天的先天性炎症(细胞因子风暴)水平最高。随着时间的推移,细胞因子水平有趋于正常的趋势。结论对细胞因子水平的时空分析可为重症儿童临床病程的神经炎症途径提供信息。目前正在对整个队列进行进一步分析,以评估纵向和组间差异。进一步了解该人群神经炎症通路的改变可能有助于合理安排靶向免疫疗法,从而改善预后。
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C.5 Altered inflammatory profiles in critically ill children with neurologic involvement
Background: More than 1 in 4 children admitted to the pediatric ICU (PICU) have suspected neuroinflammation for a variety of reasons. While often beneficial, uncontrolled inflammation can lead to secondary neurologic injuries and interfere with repair mechanisms. Methods: A prospective cohort study was initiated at Alberta Children’s Hospital to evaluate neuroinflammation in children admitted to the PICU. Forty-eight cytokines, chemokines and growth factors collected at multiple pre-determined timepoints were analyzed along with data on clinical trajectory. Preliminary exploratory analyses of patients enrolled January 2022-July 2023 were completed. Results: Fifty-three patients were included in the initial analysis. Encephalopathy (18.9%), hypoxia (17%) and TBI (15.1%) were the most common reasons for enrollment. All groups had temporal alterations in serum cytokines, with primary inflammatory brain diseases having the highest levels of innate inflammation (cytokine storm) on admission and day one compared to other subgroups. There was a trend towards normalization of cytokine levels over time. Conclusions: Temporal profiling of cytokine levels can inform on neuroinflammatory pathways contributing to the clinical course in critically ill children. Further analysis is ongoing with the entire cohort to evaluate longitudinal and between-group differences. Improved understanding of altered neuroinflammatory pathways in this population may assist with rationalizing targeted immunotherapies to improve outcomes.
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