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儿童高危脓毒症表型的代谢组学和细胞因子谱

Metabolomic and cytokine profiles of high-risk sepsis phenotypes in children.

作者信息

Hurtado Ryan R, Sanchez-Pinto L Nelson

机构信息

Department of Pediatric Intensive Care, OSF HealthCare, Children's Hospital of Illinois/University of Illinois College of Medicine, 530 NE Glen Oak Ave, 4th Fl Milestone Building, Peoria, IL, USA.

Department of Pediatrics (Critical Care) and Department of Preventive Medicine (Health and Biomedical Informatics), Northwestern University Feinberg School of Medicine, and Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.

出版信息

Sci Rep. 2025 Jul 15;15(1):25639. doi: 10.1038/s41598-025-10665-z.

Abstract

Children with sepsis are at risk of developing life-threatening multiple organ dysfunction (MODS). We have previously described two sepsis phenotypes associated with poor prognosis: "persistent hypoxemia, encephalopathy and shock" (PHES) and "sepsis-associated persistent MODS" (PMODS). We hypothesized there are unique metabolomic and cytokine profiles associated with these phenotypes that will allow for better identification and understanding of their pathophysiology. To test this, plasma samples from 50 children with sepsis-associated MODS were categorized as meeting criteria for PHES, PMODS or assigned as controls. Concentrations of 166 lipids, 26 metabolites and 20 cytokines were measured and analyzed. Of 50 patients, 17 were classified as the PHES phenotype and had upregulation of pro-inflammatory cytokines and an endothelial activation biomarker compared to controls (p < 0.05). 14 patients were classified as PMODS and had significant downregulation of immune mediators compared to controls (p < 0.05). Both phenotypes were associated with mitochondrial dysfunction based on the metabolic profiles of lysine, carnitine, and short and long chain fatty acids. Our results demonstrate metabolomic, immune, and endothelial dysregulation associated with two high-risk sepsis phenotypes in children. If validated, our findings suggest there may be several immune modulation, endothelial repair, and metabolic support therapies that could be tested in these phenotypes.

摘要

患有脓毒症的儿童有发生危及生命的多器官功能障碍(MODS)的风险。我们之前描述了两种与预后不良相关的脓毒症表型:“持续性低氧血症、脑病和休克”(PHES)和“脓毒症相关持续性多器官功能障碍”(PMODS)。我们假设存在与这些表型相关的独特代谢组学和细胞因子谱,这将有助于更好地识别和理解其病理生理学。为了验证这一点,将50例患有脓毒症相关多器官功能障碍的儿童的血浆样本分类为符合PHES、PMODS标准或指定为对照组。测量并分析了166种脂质、26种代谢物和20种细胞因子的浓度。在50例患者中,17例被分类为PHES表型,与对照组相比,促炎细胞因子和一种内皮激活生物标志物上调(p<0.05)。14例患者被分类为PMODS,与对照组相比,免疫介质显著下调(p<0.05)。基于赖氨酸、肉碱以及短链和长链脂肪酸的代谢谱,这两种表型均与线粒体功能障碍有关。我们的结果表明,儿童中两种高危脓毒症表型与代谢组学、免疫和内皮功能失调有关。如果得到验证,我们的研究结果表明,可能有几种免疫调节、内皮修复和代谢支持疗法可在这些表型中进行测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f78/12264046/2164fd037f23/41598_2025_10665_Fig1_HTML.jpg

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