Predicting Renal Replacement Therapy Requirement In Sepsis-Associated Acute Kidney Injury Using Furosemide Stress Testing and Urinary Biomarkers

Summary

This article describes a combined functional and urinary biomarker-based approach to predict renal replacement therapy requirements in patients with sepsis-associated acute kidney injury.

Abstract

This study aimed to investigate the predictive value of a model combining the furosemide stress test (FST) with urinary tissue inhibitor of metalloproteinase-2 (TIMP-2) and insulin-like growth factor-binding protein 7 (IGFBP-7) for predicting renal replacement therapy (RRT) initiation within 7 days in patients with sepsis-associated acute kidney injury (SA-AKI). A total of 63 patients with SA-AKI admitted to the intensive care units (ICU) of Zhongwei People’s Hospital and the Affiliated Hospital of Ningxia Medical University between January 2025 and November 2025 were enrolled in this study. According to whether RRT was initiated within 7 days, patients were divided into an RRT group (n = 20) and a non-RRT group (n = 43). Clinical characteristics, laboratory parameters, and urinary biomarkers were collected. Urinary TIMP-2 and IGFBP-7 levels were measured using enzyme-linked immunosorbent assay, and the predictive performance of FST combined with urinary [TIMP-2] * [IGFBP-7] was evaluated using multivariate logistic regression and receiver operating characteristic (ROC) curve analysis. The results showed that 20 patients (31.7%) required RRT during follow-up, while 43 patients (68.3%) did not. Compared with the non-RRT group, patients in the RRT group exhibited more severe renal dysfunction and higher incidence of adverse kidney events. ROC analysis demonstrated that the area under the curve (AUC) for FST, baseline TIMP-2*IGFBP-7, TIMP-2*IGFBP-7 measured 2 h after FST, and the combined model were 0.878, 0.820, 0.845, and 0.966, respectively. Multivariate logistic regression further confirmed that the combined FST and urinary TIMP-2*IGFBP-7 indicator was an independent predictor of RRT requirement. These findings suggest that the combined FST and urinary TIMP-2*IGFBP-7 model may be useful for early risk stratification of SA-AKI patients at high risk of requiring RRT.

Introduction

Sepsis is a critical clinical syndrome commonly encountered in the intensive care unit (ICU), characterized by high morbidity and mortality. The systemic inflammatory response triggered by sepsis can lead to multiple organ dysfunction, among which sepsis-associated acute kidney injury (SA-AKI) is one of the most common and severe complications^1,2,3. Previous studies have reported that approximately 40%–50% of patients with sepsis develop SA-AKI, which is associated with significantly increased mortality^4,5,6. Therefore, early identification and accurate diagnosis of SA-AKI are essential for assessing disease progression and guiding therapeutic strategies. For patients with progressive SA-AKI, timely initiation of renal replacement therapy (RRT) plays an important role in maintaining internal homeostasis and preventing multiple organ failure. However, reliable and objective criteria for determining the optimal timing of RRT initiation remain lacking in clinical practice^7,8.

In recent years, biomarkers have attracted considerable attention for the early diagnosis and risk stratification of SA-AKI^9,10,11. Tissue inhibitor of metalloproteinase-2 (TIMP-2) and insulin-like growth factor-binding protein-7 (IGFBP-7) reflect renal tubular cell cycle arrest and cellular stress responses, and have been demonstrated to possess good predictive value for the occurrence and progression of acute kidney injury^12,13. In addition, the furosemide stress test (FST) evaluates renal responsiveness to diuretics and indirectly reflects tubular functional reserve and renal perfusion status, providing a simple and practical functional assessment of kidney injury severity¹⁴. Nevertheless, a single indicator has limitations in predicting the timing of RRT initiation and may not fully capture renal function, local injury, and systemic pathophysiological changes.

Therefore, this study employed a two-center prospective diagnostic prediction model to jointly evaluate FST results and urinary [TIMP-2] * [IGFBP-7] levels in patients with SA-AKI. By integrating clinical variables and laboratory indicators, we aimed to construct a predictive model for RRT requirement within 7 days and to assess its ability to identify high-risk SA-AKI patients, thereby providing evidence to support early clinical decision-making.

Protocol

Patient enrollment and ethical approval
This study was designed as a prospective two-center cohort study. The study population consisted of patients with sepsis-associated acute kidney injury (SA-AKI) who were admitted to the intensive care units (ICU) of Zhongwei People’s Hospital and the General Hospital of Ningxia Medical University between January 2025 and November 2025. The study protocol was approved by the Ethics Committees of the General Hospital of Ningxia Medical University (Approval No. KYLL-2025-1232) and Zhongwei People’s Hospital, Ningxia, China (Approval No. NXZWSRMYYLL-202445). All procedures were conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants or their legal representatives before enrollment.

The inclusion criteria were as follows: age ≥ 18 years; diagnosis of sepsis according to the Sepsis-3.0 criteria; diagnosis of acute kidney injury according to the KDIGO 2012 criteria; and written informed consent provided by the patient or legal guardian.

The exclusion criteria were patients with end-stage renal disease (CKD stage 5) or those receiving long-term dialysis; severe hepatic dysfunction, defined as Child-Pugh class C liver disease, not related to the current sepsis episode; known allergy to furosemide; pregnant or lactating women; patients with incomplete clinical data, unavailable or incomplete urinary biomarker measurements, or inability to complete the study protocol.

During the study period, 100 patients were screened. After excluding 30 patients without sepsis, 5 patients with missing data, and 2 patients who withdrew from the study, a total of 63 patients were finally included in the analysis.

Diagnostic procedures for SA-AKI

Diagnosis of sepsis
Sepsis was diagnosed according to the Sepsis-3.0 definition^2,3. Patients were diagnosed with sepsis when a confirmed or suspected infection was present, and the Sequential Organ Failure Assessment (SOFA) score increased by ≥2 points from baseline. The diagnosis of sepsis was determined based on the following information: evidence of infection, including pulmonary infection, abdominal infection, urinary tract infection, biliary infection, or soft tissue infection; clinical manifestations, such as fever or hypothermia, chills, altered consciousness, hypotension, and hemodynamic instability; laboratory findings, including white blood cell count, procalcitonin (PCT), interleukin-6 (IL-6), and lactate levels; assessment of organ dysfunction using the SOFA score, which evaluates respiratory, cardiovascular, renal, neurological, hepatic, and coagulation functions.

Diagnosis of acute kidney injury
Acute kidney injury (AKI) was diagnosed according to the Kidney Disease: Improving Global Outcomes (KDIGO) 2012 criteria¹⁵. AKI was defined when any of the following conditions were met: An increase in serum creatinine (Scr) ≥ 26.5 µmol/L within 48 h; an increase in serum creatinine ≥ 50% from baseline; and a urine output of <0.5 mL/(kg·h) for ≥6 h. Baseline Scr was obtained from available medical records before or at admission; patients without sufficient data for KDIGO staging were excluded as incomplete clinical data. The severity of AKI was classified into stages 1, 2, and 3 according to KDIGO criteria, based on the magnitude of serum creatinine increase and the degree of urine output reduction.

Definition of SA-AKI
Patients who met both the Sepsis-3.0 criteria for sepsis and the KDIGO diagnostic criteria for acute kidney injury were defined as having sepsis-associated acute kidney injury (SA-AKI). Eligible patients meeting these criteria were subsequently included in the study.

Collection of clinical data and laboratory indicators
After confirming the diagnosis of SA-AKI, baseline demographic and clinical information were collected, including: Demographic data: age and sex; Infection-related information: infection site and patient source; Comorbidities: including hypertension, diabetes mellitus, chronic kidney disease, and cardiovascular diseases; Disease severity assessment: Acute Physiology and Chronic Health Evaluation II (APACHE II) score and SOFA score;

For AKI stage classification, laboratory indicators within the first 24 h after ICU admission were also recorded, including: white blood cell count, absolute lymphocyte count, neutrophil percentage, platelet count, blood pH, lactate, albumin, total bilirubin, serum creatinine, serum potassium, procalcitonin (PCT), and interleukin-6 (IL-6).

Furosemide stress test (FST)
The furosemide stress test (FST) was performed to assess renal tubular functional reserve and the risk of AKI progression^16,17. In the present study, FST was administered after the diagnosis of SA-AKI had been established and when patients developed clinical signs of fluid overload during early ICU management. The predefined indications for FST included positive cumulative fluid balance exceeding 5% of baseline body weight, newly developed dyspnea, or peripheral edema. FST was performed according to a standardized protocol. Furosemide was administered intravenously at a dose of 1.0–1.5 mg/kg, and total urine output was measured during the subsequent 2 h. A urine output of ≥200 mL within 2 h after furosemide administration was defined as FST responsive, whereas a urine output of <200 mL was defined as FST nonresponsive/high risk. Blood pressure, urine catheter patency, fluid balance, and serum potassium were monitored during the test.

Measurement of urinary biomarkers
Urine samples were collected at the following time points: 0 h (baseline), 2 h after FST, 4 h after FST, and 12 h after FST. During the observation period, a small number of patients had markedly reduced urine output; however, complete anuria was not observed in the final analytic cohort. For patients with severely reduced urine volume, urine samples were collected whenever possible, according to the study protocol. Patients with unavailable or incomplete urinary biomarker measurements were excluded during patient screening and data quality control. The sample processing procedure was as follows. Urine samples were centrifuged within 2 h after collection. Centrifugation was performed at 151 × g for 15 min. The supernatant was then transferred to sterile tubes and stored at −80 °C until analysis. Before measurement, the samples were thawed and centrifuged again. The concentrations of tissue inhibitor of metalloproteinase-2 (TIMP-2) and insulin-like growth factor-binding protein 7 (IGFBP-7) were determined using enzyme-linked immunosorbent assay (ELISA), and the product of urinary [TIMP-2] * [IGFBP-7] was calculated^11,13. RRIDs were unavailable for the commercial kits used in this study. Urinary biomarker values were not normalized to urinary creatinine.

Construction of the predictive model
The primary endpoint of the study was the initiation of renal replacement therapy (RRT) within 7 days after enrollment. RRT was initiated according to routine clinical indications, including refractory hyperkalemia, refractory acidosis, fluid overload, oliguria/anuria, or uremic complications. Patients were divided into two groups based on whether RRT was initiated within 7 days: RRT group and non-RRT group. The predictive model was constructed as follows. First, baseline characteristics, laboratory indicators, FST results, AKI stage, and urinary biomarker levels were compared between the two groups to identify potential variables associated with RRT requirement. Second, univariate logistic regression analysis was performed to evaluate the association between candidate variables and the need for RRT within 7 days. Third, variables with P < 0.10 in the univariate analysis, together with AKI stage, given its clinical relevance to RRT requirement, were included in the multivariate logistic regression model to identify independent predictors after adjusting for potential confounding factors. Particular emphasis was placed on evaluating the predictive value of the combined index of FST and urinary [TIMP-2] * [IGFBP-7]. Because FST was administered according to predefined clinical indications rather than at a prespecified fixed time point after ICU admission, the exact timing of FST administration was not prespecified as a candidate predictor in the primary multivariable model.

Evaluation of predictive performance
Receiver operating characteristic (ROC) curve analysis was used to assess how well each individual indicator and the combined model identified patients who required RRT within 7 days. The area under the curve (AUC), sensitivity, and specificity were determined. The following indicators were compared: Baseline urinary [TIMP-2] * [IGFBP-7]; FST results; Urinary [TIMP-2] * [IGFBP-7] measured 2 h after FST; The combined model incorporating FST and urinary [TIMP-2] * [IGFBP-7] at 2 h after FST. The predictive performance of the combined model was evaluated by comparing AUC values with those of individual indicators. Net reclassification improvement (NRI) for the 2-h biomarker model is presented in Supplemental Table S1.

Statistical analysis
Normally distributed continuous variables were reported as mean ± standard deviation (SD) and compared between groups using the independent-samples t-test. Continuous variables with non-normal distributions were reported as median (interquartile range) and compared using the Wilcoxon rank-sum test. Categorical variables were analyzed using the chi-square test or Fisher’s exact test. Logistic regression was used to assess factors associated with RRT requirement, with odds ratios (ORs) and 95% confidence intervals (CIs) reported. ROC curves were compared using the DeLong test. All tests were two-sided, and P < 0.05 was considered statistically significant.

Results

Patient enrollment and baseline characteristics
A total of 100 patients were initially screened in this study. After excluding 30 patients without sepsis, 5 patients with missing data, and 2 patients who withdrew from the study, a total of 63 patients with confirmed sepsis-associated acute kidney injury (SA-AKI) were finally included in the analysis. Among them, 42 were male, and 21 were female, with a mean age of 67.25 ± 14.5 years. Based on whether renal replacement therapy (RRT) was initiated with...

Discussion

Sepsis-associated acute kidney injury (SA-AKI) is a common and severe complication in patients admitted to the intensive care unit (ICU). Its pathophysiological mechanisms are complex and involve multiple processes, including inflammatory responses, microcirculatory dysfunction, and oxidative stress¹⁸. Timely and appropriate initiation of renal replacement therapy (continuous renal replacement therapy, CRRT) is critical for improving the prognosis of patients with SA-AKI. However, the optimal timi...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Automated Biochemical Analyzer	Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, China	BS-800
Biosafety Cabinet	Airtech (Suzhou) Co., Ltd., Suzhou, China	BSC-1300IIA2
Blood Gas Analyzer	Edan Instruments, Inc., Shenzhen, China	i15
Centrifuge (Low-speed refrigerated centrifuge)	Xiangyi Centrifuge Instrument Co., Ltd., Changsha, China	H1850
ELISA Kit for IGFBP-7	Elabscience Biotechnology Co., Ltd., Wuhan, China	E-EL-H5567
ELISA Kit for TIMP-2	Elabscience Biotechnology Co., Ltd., Wuhan, China	E-EL-H0003
ELISA Microplate Reader	Rayto Life and Analytical Sciences Co., Ltd., Shenzhen, China	RT-6100
ELISA Plate Washer	Rayto Life and Analytical Sciences Co., Ltd., Shenzhen, China	RT-2600C
Furosemide	Not specified in submission files	Not specified in submission files	Administered intravenously at 1.0–1.5 mg/kg for FST
Infusion Pump	Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, China	BeneFusion SP5
Micropipette	Dragon Laboratory Instruments Co., Ltd., Shanghai, China	TopPette
Microplate (96-well ELISA plate)	Elabscience Biotechnology Co., Ltd., Wuhan, China	E-EL-Plate96
Multiparameter Patient Monitor	Mindray Bio-Medical Electronics Co., Ltd., Shenzhen, China	BeneVision N12
Pipette Tips (200 μL)	Dragon Laboratory Instruments Co., Ltd., Shanghai, China	T-200
R software	Not specified in submission files	Not specified in submission files	Used for statistical analyses
Refrigerated Storage (4 °C Medical Refrigerator)	Haier Biomedical Co., Ltd., Qingdao, China	HYC-290
Sterile Sample Tubes	Kangjian Medical Supplies Co., Ltd., Jiangsu, China	KJ-ST02
Ultra-Low Temperature Freezer (-80 °C)	Haier Biomedical Co., Ltd., Qingdao, China	DW-86L388
Urine Collection Tubes	Kangjian Medical Supplies Co., Ltd., Jiangsu, China	KJ-UT01