Plasma YAP1 as a biomarker for the prediction of occurrence, progression, and outcomes of sepsis-associated liver injury: a prospective observational study.

IF 2.5 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Jun Shao, Lulu Zhou, Haoran Wang, Xiaohua Gu, Tianwei Wang, Tingting Yu, Jichao Zhai, Aipeng Hu, Yuanyuan Zhu, Wei Lei, Hailong Yu, Nianfang Lu, Ruiqiang Zheng
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引用次数: 0

Abstract

Background: Sepsis-associated liver injury (SALI) is an independent risk factor for multiple organ dysfunction and high mortality in septic patients, which is often associated with a poor prognosis. Currently, there is still a lack of early diagnostic biomarkers of Sepsis-Associated Liver Injury in clinical practice. YAP1 (Yes1 Associated Transcriptional Regulator) has been demonstrated to correlate with hepatic inflammation, nevertheless, its exact function and mechanism in sepsis-associated liver injury have not been conclusively determined.

Methods: Clinical data of septic patients in the ICU of Northern Jiangsu People's Hospital (Oct. 2023 - Dec. 2025) were reviewed. Patients were classified into sepsis non-liver injury (SNLI) and SALI groups according to the presence or absence of liver injury at admission. Logistic regression was used to identify independent risk factors for SALI. Receiver operating characteristic (ROC) analysis assessed predictive performance. Patients were stratified by plasma YAP1 quartiles to evaluate its association with disease progression, and significant variables were further analyzed by logistic regression. Correlations were examined using Spearman analysis. A Cox proportional hazards model was applied to assess the association between YAP1 and 28-day mortality in SALI patients.

Results: A total of 199 patients were included (SNLI, n = 121; SALI, n = 78). Plasma YAP1 was an independent protective factor for SALI (OR = 0.97, P < 0.001), while BMI (OR = 1.35, P = 0.015) and day 1 lactate (OR = 1.48, P = 0.002) were independent risk factors. YAP1 showed good predictive performance (AUC = 0.86). Higher YAP1 levels were independently associated with 72-hour SOFA score reduction (OR = 7.55, P = 0.009), indicating improved early organ function. No significant association was found between YAP1 and 28-day mortality.

Conclusion: Plasma YAP1 is inversely associated with SALI occurrence and demonstrates good predictive performance. Higher YAP1 levels are associated with early organ function improvement but not with 28-day mortality.

血浆YAP1作为预测败血症相关肝损伤发生、进展和结局的生物标志物:一项前瞻性观察性研究
背景:脓毒症相关性肝损伤(SALI)是脓毒症患者多器官功能障碍和高死亡率的独立危险因素,常伴有预后不良。目前,临床实践中仍缺乏脓毒症相关肝损伤的早期诊断生物标志物。YAP1 (Yes1相关转录调节因子)已被证明与肝脏炎症相关,然而,其在脓毒症相关肝损伤中的确切功能和机制尚未确定。方法:回顾苏北人民医院重症监护室感染性疾病患者的临床资料(2023年10月- 2025年12月)。根据入院时有无肝损伤,将患者分为脓毒症非肝损伤组(SNLI)和SALI组。采用Logistic回归确定SALI的独立危险因素。受试者工作特征(ROC)分析评估预测效果。以血浆YAP1四分位数对患者进行分层,评估其与疾病进展的相关性,并通过logistic回归进一步分析显著变量。使用Spearman分析检验相关性。应用Cox比例风险模型评估SALI患者YAP1与28天死亡率之间的关系。结果:共纳入199例患者(SNLI, n = 121; SALI, n = 78)。血浆YAP1是SALI的独立保护因子(OR = 0.97, P)。结论:血浆YAP1与SALI的发生呈负相关,具有良好的预测作用。较高的YAP1水平与早期器官功能改善有关,但与28天死亡率无关。
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来源期刊
BMC Gastroenterology
BMC Gastroenterology 医学-胃肠肝病学
CiteScore
4.20
自引率
0.00%
发文量
465
审稿时长
6 months
期刊介绍: BMC Gastroenterology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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