Organ Support and Automation Technologies, United States Army Institute of Surgical Research, Fort Sam Houston, TX, United States.
Long School of Medicine, University of Texas Health Science Center, San Antonio, TX, United States.
Front Immunol. 2024 Oct 29;15:1447597. doi: 10.3389/fimmu.2024.1447597. eCollection 2024.
Acute kidney injury (AKI) and multiple organ failure (MOF) are leading causes of mortality in trauma injuries. Early diagnosis of AKI and MOF is vital to improve outcomes, but current diagnostic criteria rely on laboratory markers that are delayed or unreliable. In this study, we investigated whether damage associated molecular patterns such as high-mobility group box 1 (HMGB1), syndecan-1 (SDC-1) and C3a correlate with the development of trauma-induced AKI and MOF.
Thirty-nine swine underwent smoke inhalation and severe burns, then received critical care for 72 hours or until death. AKI was defined by the KDIGO (Kidney Disease: Improving Global Outcomes) criteria, which labels AKI when a 1.5-fold increase in blood creatinine levels from baseline or a urine output < 0.5 mL/kg/h for 6 hours or more occurs. MOF was defined by the presence of both AKI and acute respiratory distress syndrome (PaO/FiO<300 for 4 hours).
Eight of 39 pigs developed AKI and seven of those developed MOF. Pathological analysis revealed that polytrauma induces significantly higher kidney injury scores compared to sham controls. The average time from injury to KDIGO AKI was 24 hours (interquartile range: 22.50-32.25). Twelve hours after injury, HMGB1 levels were significantly increased in animals that went on to develop AKI compared to those that did not (73.07 ± 18.66 ng/mL vs. 31.64 ± 4.15 ng/mL, <0.01), as well as in animals that developed MOF compared to those that did not (81.52±19.68 ng/mL vs. 31.19 ± 3.972 ng/mL, <0.05). SDC-1 and C3a levels were not significantly different at any time point between groups. ROC analysis revealed that HMGB1 levels at 12 hours post-injury were predictive of both AKI and MOF development (AKI: AUROC=0.81, cut-off value=36.41 ng/mL; MOF: AUROC=0.89, cut-off value=36.41 ng/mL). Spearman's correlation revealed that HMGB1 levels at 12 hours correlated with multiple parameters of AKI, including blood urea nitrogen, blood creatinine, and blood myoglobin.
Twelve-hour post-injury HMGB1 levels predict AKI and MOF in a smoke inhalation and burn swine model. Further research is needed to validate this result in other polytrauma models and in critical combat causalities.
急性肾损伤(AKI)和多器官功能衰竭(MOF)是创伤性损伤导致死亡的主要原因。早期诊断 AKI 和 MOF 对于改善预后至关重要,但目前的诊断标准依赖于实验室标志物,这些标志物存在延迟或不可靠的问题。在这项研究中,我们研究了高迁移率族蛋白 B1(HMGB1)、硫酸乙酰肝素蛋白聚糖 1(SDC-1)和 C3a 等损伤相关分子模式是否与创伤诱导的 AKI 和 MOF 的发生相关。
39 头猪经历了烟雾吸入和严重烧伤,然后接受了 72 小时的重症监护,或者直到死亡。AKI 是根据 KDIGO(肾脏病:改善全球预后)标准定义的,当血液肌酐水平从基线升高 1.5 倍或尿液输出量<0.5 mL/kg/h 持续 6 小时以上时,就会发生 AKI。MOF 是指同时存在 AKI 和急性呼吸窘迫综合征(PaO/FiO<300 持续 4 小时)。
39 头猪中有 8 头发生了 AKI,其中 7 头发生了 MOF。病理分析显示,多发伤导致的肾脏损伤评分明显高于假手术对照组。从损伤到 KDIGO AKI 的平均时间为 24 小时(四分位距:22.50-32.25)。损伤后 12 小时,发生 AKI 的动物的 HMGB1 水平明显高于未发生 AKI 的动物(73.07±18.66ng/mL 比 31.64±4.15ng/mL,<0.01),发生 MOF 的动物的 HMGB1 水平也明显高于未发生 MOF 的动物(81.52±19.68ng/mL 比 31.19±3.972ng/mL,<0.05)。SDC-1 和 C3a 水平在任何时间点在组间均无显著差异。ROC 分析显示,损伤后 12 小时的 HMGB1 水平可预测 AKI 和 MOF 的发生(AKI:AUROC=0.81,截断值=36.41ng/mL;MOF:AUROC=0.89,截断值=36.41ng/mL)。Spearman 相关分析显示,损伤后 12 小时的 HMGB1 水平与 AKI 的多个参数相关,包括血尿素氮、血肌酐和血肌红蛋白。
在烟雾吸入和烧伤猪模型中,损伤后 12 小时的 HMGB1 水平可预测 AKI 和 MOF。需要进一步研究以在其他多发伤模型和重症战斗伤员中验证这一结果。