脓毒症的坏死和凋亡途径:儿科和成人ICU患者的比较分析。

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
George Briassoulis, Konstantina Tzermia, Kalliopi Bastaki, Marianna Miliaraki, Panagiotis Briassoulis, Athina Damianaki, Eumorfia Kondili, Stavroula Ilia
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引用次数: 0

摘要

背景:坏死性上睑下垂是炎症细胞死亡的一种调控形式,越来越被认为是脓毒症和危重疾病的关键驱动因素。坏死下垂和细胞凋亡之间的平衡可能影响ICU患者的免疫反应和预后。目的:评估患有败血症/感染性休克、创伤/SIRS或心脏病的危重儿科和成人患者中坏死性上睑塌陷和细胞凋亡相关蛋白的表达,并评估其与临床结果的关系。方法:在这项前瞻性观察性研究中,88例三级ICU住院患者被分为四组:败血症/感染性休克、创伤/SIRS、心脏病和健康对照。采用ELISA法测定入院24 h内血清RIPK1、RIPK3、MLKL、A20、caspase-8、IL-1β、IL-18水平。按疾病组、年龄和严重程度指标分析生物标志物。结果:脓毒症患者(成人和儿童)均表现出RIPK1、IL-1β和IL-18水平显著升高(p < 0.001), caspase-8水平降低(p = 0.015),表明坏死下垂途径被激活。A20显著上调(p < 0.001),且与乳酸水平独立相关。RIPK1、IL-1β和IL-18与ICU住院时间和病情严重程度呈正相关,caspase-8呈负相关。ROC分析显示RIPK1 (AUC = 0.81)、IL-18 (AUC = 0.71)和A20 (AUC = 0.71)对脓毒症/感染性休克具有较强的预测能力;相反,caspase-8与脓毒症呈负相关(AUC = 0.32)。结论:坏死性上睑下垂似乎在脓毒症的病理生理中起着核心作用。RIPK1、IL-1β、IL-18和A20水平的升高可以作为疾病严重程度的生物标志物,而caspase-8的降低支持细胞凋亡向坏死细胞死亡的转变。这些发现强调了坏死相关通路作为所有年龄危重患者风险分层和治疗干预目标的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Necroptotic and Apoptotic Pathways in Sepsis: A Comparative Analysis of Pediatric and Adult ICU Patients.

Background: Necroptosis, a regulated form of inflammatory cell death, is increasingly recognized as a key driver of sepsis and critical illness. The balance between necroptosis and apoptosis may influence immune responses and outcomes in ICU patients. Objective: To evaluate necroptosis- and apoptosis-related protein expression in critically ill pediatric and adult patients with sepsis/septic shock, trauma/SIRS, or cardiac conditions, and assess their association with clinical outcomes. Methods: In this prospective, observational study, 88 patients admitted to a tertiary ICU were categorized into four groups: sepsis/septic shock, trauma/SIRS, cardiac disease, and healthy controls. Serum levels of RIPK1, RIPK3, MLKL, A20, caspase-8, IL-1β, and IL-18 were measured within 24 h of admission using ELISA. Biomarkers were analyzed by disease group, age, and severity indices. Results: Patients with sepsis-both adults and children-exhibited significantly elevated levels of RIPK1, IL-1β, and IL-18 (p < 0.001) and reduced levels of caspase-8 (p = 0.015), indicating activation of the necroptosis pathway. A20 was significantly upregulated (p < 0.001) and independently associated with lactate levels. RIPK1, IL-1β, and IL-18 were positively correlated with ICU length of stay and illness severity, whereas caspase-8 showed an inverse correlation. ROC analysis demonstrated strong predictive performance for sepsis/septic shock using RIPK1 (AUC = 0.81), IL-18 (AUC = 0.71), and A20 (AUC = 0.71); conversely, caspase-8 was inversely associated with sepsis (AUC = 0.32). Conclusions: Necroptosis appears to play a central role in the pathophysiology of sepsis across age groups. Elevated levels of RIPK1, IL-1β, IL-18, and A20 may serve as biomarkers of disease severity, while reduced caspase-8 supports a shift away from apoptosis toward necroptotic cell death. These findings highlight the potential of necroptosis-related pathways as targets for risk stratification and therapeutic intervention in critically ill patients of all ages.

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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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