Zhan Liying, Zhang Ying, Zhang Yuxin, Chen Jingdi, Zou Handong, Wang Lu, Guo Mengmeng, Huang Raojuan, Sun Yaqi, Gao Hang, Xu Jing, Xiong Ru, Wu Wei
Department of Critical Care Medicine, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Department of Vascular Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Clin Kidney J. 2025 Apr 9;18(4):sfaf095. doi: 10.1093/ckj/sfaf095. eCollection 2025 Apr.
The fibrinogen-to-albumin ratio (FAR), a novel inflammatory biomarker, is strongly associated with the incidence of sepsis. Nonetheless, there is a lack of research regarding the FAR and prognosis in individuals with septic acute kidney injury (SAKI). The aim of this study was to assess the correlation between the FAR upon intensive care unit (ICU) admission and overall mortality in patients with SAKI.
All patient information was retrieved from the Medical Information Mart for Intensive Care-IV (MIMIC-IV) database. All patients were divided into four distinct categories according to the FAR. The primary endpoints for this study were the 30-day and 365-day all-cause death rates, whereas the secondary endpoints were the 60-day, 90-day and 180-day all-cause death rates. The FAR was quartile, and the Kaplan-Meier curve was used to evaluate the outcomes across the groups. To evaluate the correlation between the FAR and outcomes, we used a Cox proportional hazards regression model and restricted cubic splines (RCSs).
Among the 6208 participants, the average age was 65 years, with 3659 (58.94%) identified as male. Patients exhibiting elevated FAR values demonstrated an increased risk of all-cause mortality at 30, 60, 90, 180 and 365 days, as evidenced by the Kaplan-Meier curves (log-rank < .001). SAKI patients with elevated FAR values had a greater risk of all-cause mortality at 30, 60, 90, 180 and 365 days than did those with lower FAR values, as demonstrated by Cox proportional hazards regression analysis. With inflection points at 35.14 for 30-day mortality and 34.8 for 365-day mortality, the RCS analysis revealed that the FAR and all-cause mortality were related in an inverted N-type pattern. In instances where FAR levels were below 35.14 mg/g, a reduction of 1 unit in the FAR correlated with a 6.5% increase in the risk of 30-day all-cause mortality [hazard ratio (HR) 0.935; 95% confidence interval (CI) 0.923, 0.948]. In instances where FAR levels were below 34.8 mg/g, a reduction of 1 unit in the FAR correlated with a 6.2% increase in the risk of 365-day all-cause mortality (HR 0.938; 95% CI 0.927, 0.949).
In severely ill patients with SAKI, elevated FAR levels are strongly correlated with an increased risk of all-cause mortality at 30, 60, 90, 180 and 365 days. FAR may serve as a reliable metric for assessing and managing patients with SAKI in the ICU.
纤维蛋白原与白蛋白比值(FAR)作为一种新型炎症生物标志物,与脓毒症的发病率密切相关。然而,关于FAR与脓毒性急性肾损伤(SAKI)患者预后的研究尚显不足。本研究旨在评估重症监护病房(ICU)入院时FAR与SAKI患者全因死亡率之间的相关性。
所有患者信息均取自重症监护医学信息集市 - 第四版(MIMIC-IV)数据库。根据FAR将所有患者分为四个不同类别。本研究的主要终点为30天和365天全因死亡率,次要终点为60天、90天和180天全因死亡率。FAR被分为四分位数,并采用Kaplan-Meier曲线评估各组的预后情况。为评估FAR与预后之间的相关性,我们使用了Cox比例风险回归模型和受限立方样条(RCS)。
在6208名参与者中,平均年龄为65岁,其中3659名(58.94%)为男性。Kaplan-Meier曲线显示,FAR值升高的患者在30、60、90、180和365天的全因死亡风险增加(对数秩<0.001)。Cox比例风险回归分析表明,FAR值升高的SAKI患者在30、60、90、180和365天的全因死亡风险高于FAR值较低的患者。RCS分析显示,30天死亡率的拐点为35.14,365天死亡率的拐点为34.8,FAR与全因死亡率呈倒N型相关。当FAR水平低于35.14mg/g时,FAR每降低1个单位,30天全因死亡风险增加6.5%[风险比(HR)0.935;95%置信区间(CI)0.923,0.948]。当FAR水平低于34.8mg/g时,FAR每降低1个单位,365天全因死亡风险增加6.2%(HR 0.938;95%CI 0.927,0.949)。
在患有SAKI的重症患者中,FAR水平升高与30、60、90、180和365天全因死亡风险增加密切相关。FAR可作为评估和管理ICU中SAKI患者的可靠指标。