Li Yuan , Yongshuang Zhou , Ruiyu Wang , Xin Huang , Ruilin Tang , Fang Yan
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引用次数: 0
Abstract
Background
Acute kidney injury (AKI) is common in septic patients and strongly associated with adverse outcomes. The pathophysiology of AKI in septic patients remains elusive, and detection of patients at risk of AKI or at risk of progression to severe and persistent AKI is critical for timely and adequate support measures, including mitigating further renal damage. Therefore, identification of biomarkers associated with septic-associated AKI that contribute to improve septic AKI is an area of intensive research.
Methods
A total of 116 consecutive patients with sepsis were categorized into two groups (AKI and non-AKI) based on the occurrence of AKI within 24 h of admission to the intensive care unit (ICU). Serum levels of soluble TLR2 (sTLR2), as well as biomarkers such as interleukin(IL)-6, IL-22, IL-10, creatinine, urea, procalcitonin, hypersensitive C-reactive protein (hs-CRP), and D-Dimer (D2), were measured within 24 h after ICU admission. Demographic and clinical characteristics including sequential organ failure assessment (SOFA) scores and acute physiology and chronic health evaluation II (APACHE II) scores were recorded. Logistic regression analysis was conducted to identify potential predictive biomarkers. Receiver operating characteristic (ROC) curve analysis was employed to determine the optimal model for predicting septic-associated AKI.
Results
Patients in the AKI group exhibited significantly higher serum concentrations of IL-6, IL-10, sTLR2, creatinine, urea, hs-CRP, procalcitonin, D2 and lower serum albumin concentrations as well as higher APACHE II scores compared to those in the non-AKI group. Logistic regression analysis revealed that APACHE II scores, log10-transformed sTLR2 concentration, creatinine and D2 concentration were valuable predictors of AKI among septic patients. ROC curves demonstrated that log10-transformed sTLR2 concentration exhibited comparable predictive value to creatinine in determining the incidence of sepsis-associated AKI. The model with variables of APACHE II score, Log10-transformed serum TLR2 concentration, creatinine and D2 concentration yielded the greatest area under the curve of 0.863.
Conclusion
Elevated levels of sTLR2 in early-stage of septic patients may serve as a promising novel biomarker for predicting sepsis-associated AKI.
背景:急性肾损伤(AKI)是脓毒症患者的常见病,与不良预后密切相关。脓毒症患者急性肾损伤的病理生理学仍然难以捉摸,而检测有急性肾损伤风险或有进展为严重和持续性急性肾损伤风险的患者对于及时采取适当的支持措施(包括减轻进一步的肾损伤)至关重要。因此,鉴定与脓毒症相关性 AKI 有关的生物标志物以改善脓毒症 AKI 是一个需要深入研究的领域:方法:根据脓毒症患者入住重症监护室(ICU)后 24 小时内发生 AKI 的情况,将 116 名脓毒症患者分为两组(AKI 组和非 AKI 组)。研究人员在患者入住重症监护室 24 小时内测量了血清中可溶性 TLR2(sTLR2)的水平,以及白细胞介素(IL)-6、IL-22、IL-10、肌酐、尿素、降钙素原、超敏 C 反应蛋白(hs-CRP)和 D-二聚体(D2)等生物标志物。记录了人口统计学和临床特征,包括序贯器官衰竭评估(SOFA)评分和急性生理学和慢性健康评估 II(APACHE II)评分。进行逻辑回归分析以确定潜在的预测性生物标记物。采用接收者操作特征(ROC)曲线分析来确定预测脓毒症相关性 AKI 的最佳模型:结果:与非 AKI 组患者相比,AKI 组患者血清中 IL-6、IL-10、sTLR2、肌酐、尿素、hs-CRP、降钙素原、D2 的浓度明显升高,血清白蛋白浓度降低,APACHE II 评分升高。逻辑回归分析显示,APACHE II 评分、经 log10 变形的 sTLR2 浓度、肌酐和 D2 浓度是脓毒症患者发生 AKI 的重要预测指标。ROC 曲线显示,在确定脓毒症相关性 AKI 的发生率方面,对数 10 变形的 sTLR2 浓度与肌酐具有相当的预测价值。包含 APACHE II 评分、血清 TLR2 浓度对数 10 变形值、肌酐和 D2 浓度等变量的模型得出的曲线下面积最大,为 0.863:脓毒症患者早期的 sTLR2 水平升高可作为预测脓毒症相关性 AKI 的新型生物标记物。
期刊介绍:
The journal Cytokine has an open access mirror journal Cytokine: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
* Devoted exclusively to the study of the molecular biology, genetics, biochemistry, immunology, genome-wide association studies, pathobiology, diagnostic and clinical applications of all known interleukins, hematopoietic factors, growth factors, cytotoxins, interferons, new cytokines, and chemokines, Cytokine provides comprehensive coverage of cytokines and their mechanisms of actions, 12 times a year by publishing original high quality refereed scientific papers from prominent investigators in both the academic and industrial sectors.
We will publish 3 major types of manuscripts:
1) Original manuscripts describing research results.
2) Basic and clinical reviews describing cytokine actions and regulation.
3) Short commentaries/perspectives on recently published aspects of cytokines, pathogenesis and clinical results.