Tianjin Medical Journal ›› 2025, Vol. 53 ›› Issue (3): 262-266.doi: 10.11958/20242152

• Clinical Research • Previous Articles     Next Articles

The predictive value of serum HMGB1 and sRAGE in the occurrence and short-term prognosis of sepsis-associated encephalopathy

ZHANG Yuxuan1(), LIU Yidan2, CHEN Zhe3, ZHANG Wen3, LI Ruixuan3, YAN Qiang3, XU Guiping3,()   

  1. 1 Graduate School of Xinjiang Medical University, Urumqi 830000, China
    2 Department of Anesthesiology, Affiliated Cancer Hospital of Xinjiang Medical University
    3 Department of Anesthesiology, People's Hospital of Xinjiang Uygur Autonomous Region, Xinjiang Clinical Research Center for Anesthesia Managemen
  • Received:2024-12-07 Revised:2025-01-18 Published:2025-03-15 Online:2025-03-31
  • Contact: E-mail:xuguipingmzk@163.com

Abstract:

Objective To explore the predictive value of serum high-mobility group box protein B1 (HMGB1) and soluble receptor for advanced glycation end-products (sRAGE) in the occurrence and short-term prognosis of sepsis-associated encephalopathy (SAE). Methods Clinical data of 228 patients with sepsis were retrospectively analyzed. According to the presence of SAE, patients were divided into the SAE group (96 cases) and the non-SAE group (132 cases). General clinical data, laboratory test results, Acute Physiology and Chronic Health Evaluation Ⅱ (APACHEⅡ) scores, Sequential Organ Failure Assessment (SOFA) scores and serum HMGB1 and sRAGE levels were compared between the two groups. Multivariate Logistic regression analysis was performed to determine factors influencing SAE occurrence. Receiver operating characteristic (ROC) curves were plotted to evaluate the predictive ability of HMGB1, sRAGE and the HMGB1/sRAGE ratio to predict the occurrence and short-term prognosis of SAE. Kaplan-Meier survival curves were used to compare the 28-day mortality rates of SAE patients with different HMGB1 and sRAGE expression levels. Results Compared to the non-SAE group, patients in the SAE group exhibited elevated serum HMGB1 levels, decreased sRAGE levels and an increased HMGB1/sRAGE ratio (P<0.05). The areas under the curve (AUC) for predicting SAE using HMGB1, sRAGE and the HMGB1/sRAGE ratio were 0.826 (95% CI: 0.770-0.872), 0.682 (95% CI: 0.617-0.742) and 0.895 (95% CI: 0.848-0.932), respectively, indicating predictive value. Among the 96 SAE patients, 52 (54.2%) died within 28 days. There were no statistically significant differences in HMGB1, sRAGE and the HMGB1/sRAGE ratio between surviving and deceased patients (P>0.05). Similarly, there were no significant differences in 28-day mortality rates between SAE patients with different HMGB1 or sRAGE expression levels. Conclusion Elevated serum HMGB1 and reduced sRAGE are of significant value in the auxiliary diagnosis of SAE, but have limited clinical predictive value for short-term prognosis.

Key words: sepsis-associated encephalopathy, HMGB1 protein, receptor for advanced glycation end products, prognosis

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