Association Between Metabolic and Inflammatory Biomarkers and Prognosis in Traumatic Brain Injury: A Focus on Short- and Medium-Term Mortality.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-05-12 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S519606
Hua Liu, Jinrong Wang, Wenming Wang, Min Ruan, Jiangang Liu
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Abstract

Background: Traumatic brain injury (TBI) is a leading cause of disability and death worldwide, involving complex pathophysiological responses such as metabolic disturbance and systemic inflammation. This study aimed to evaluate the prognostic value of selected metabolic and inflammatory biomarkers in predicting short- and medium-term mortality in patients with moderate-to-severe TBI.

Methods: We conducted a retrospective cohort study of patients with TBI admitted between March 29, 2018, and July 31, 2023. Clinical data, including a panel of metabolic (eg, triglyceride-glucose index [TYG], APOB/A1 ratio) and inflammatory biomarkers (eg, neutrophil-to-platelet ratio [NPR]), were collected within 24 hours of admission. Mortality was assessed at 14 days, 30 days, and hospital discharge. Multivariate Cox regression models and ROC curve analysis were used to assess prognostic associations and model performance.

Results: A total of 2555 patients were enrolled, of whom 579 (22.67%) underwent surgical treatment. Multivariate Cox proportional hazards regression analysis revealed that the triglyceride-glucose index (TYG) was an independent predictor of short-term mortality in TBI patients, while the neutrophil-to-platelet ratio (NPR) and apolipoprotein B/A1 (APOB/A1) ratio were independent predictors of both short- and mid-term mortality. In addition, surgical treatment was associated with an increased risk of mid-term mortality, while tracheostomy significantly reduced mortality risk across all time points. Receiver operating characteristic (ROC) curve analysis showed that the regression model incorporating inflammatory markers had the highest areas under the curve (AUCs) of 0.904, 0.897, and 0.897, demonstrating superior performance in predicting short- and mid-term mortality. Additionally, in the subgroup analysis of non-operation patients, TYG and NPR had a more significant impact on mortality risk.

Conclusion: Metabolic and inflammatory biomarkers, including TYG, NPR, and APOB/A1 ratio, provide valuable prognostic information in patients with TBI. These markers may assist clinicians in early risk stratification and personalized treatment planning.

外伤性脑损伤中代谢和炎症生物标志物与预后的关系:对中短期死亡率的关注。
背景:外伤性脑损伤(TBI)是世界范围内致残和死亡的主要原因,涉及复杂的病理生理反应,如代谢紊乱和全身炎症。本研究旨在评估选定的代谢和炎症生物标志物在预测中重度TBI患者中短期和中期死亡率方面的预后价值。方法:我们对2018年3月29日至2023年7月31日期间入院的TBI患者进行了回顾性队列研究。入院24小时内收集临床数据,包括代谢(如甘油三酯-葡萄糖指数[TYG]、APOB/A1比值)和炎症生物标志物(如中性粒细胞与血小板比值[NPR])。在14天、30天和出院时评估死亡率。采用多变量Cox回归模型和ROC曲线分析评估预后相关性和模型性能。结果:共纳入2555例患者,其中579例(22.67%)接受手术治疗。多因素Cox比例风险回归分析显示,甘油三酯-葡萄糖指数(TYG)是TBI患者短期死亡率的独立预测因子,而中性粒细胞与血小板比值(NPR)和载脂蛋白B/A1 (APOB/A1)比值是TBI患者短期和中期死亡率的独立预测因子。此外,手术治疗与中期死亡风险增加相关,而气管切开术在所有时间点均可显著降低死亡风险。受试者工作特征(ROC)曲线分析显示,纳入炎症标志物的回归模型曲线下面积(auc)最高,分别为0.904、0.897和0.897,在预测中短期死亡率方面表现优异。此外,在非手术患者的亚组分析中,TYG和NPR对死亡风险的影响更为显著。结论:代谢和炎症生物标志物,包括TYG、NPR和APOB/A1比值,为TBI患者的预后提供了有价值的信息。这些标志物可以帮助临床医生进行早期风险分层和个性化治疗计划。
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
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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