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Abstract
Acute kidney injury (AKI) is a common condition in hospitalized patients who often requires kidney support therapy (KST). However, predicting the need for KST in critically ill patients remains challenging. This study aimed to analyze endothelium-related biomarkers as predictors of KST need in critically ill patients with stage 2 AKI. A prospective observational study was conducted on 127 adult ICU patients with stage 2 AKI by serum creatinine only. Endothelium-related biomarkers, including vascular cell adhesion protein-1 (VCAM-1), angiopoietin (AGPT) 1 and 2, and syndecan-1, were measured. Clinical parameters and outcomes were recorded. Logistic regression models, receiver operating characteristic (ROC) curves, continuous net reclassification improvement (NRI) and integrated discrimination improvement (IDI) were used for analysis. Among the patients, 22 (17.2%) required KST within 72 h. AGPT2 and syndecan-1 levels were significantly greater in patients who progressed to the KST. Multivariate analysis revealed that AGPT2 and syndecan-1 were independently associated with the need for KST. The area under the ROC curve (AUC-ROC) for AGPT2 and syndecan-1 performed better than did the constructed clinical model in predicting KST. The combination of AGPT2 and syndecan-1 improved the discrimination capacity of predicting KST beyond that of the clinical model alone. Additionally, this combination improved the classification accuracy of the NRI and IDI. AGPT2 and syndecan-1 demonstrated predictive value for the need for KST in critically ill patients with stage 2 AKI. The combination of AGPT2 and syndecan-1 alone enhanced the predictive capacity of predicting KST beyond clinical variables alone. These findings may contribute to the early identification of patients who will benefit from KST and aid in the management of AKI in critically ill patients.
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Details
1 Rede Nordeste de Biotecnologia - RENORBIO, Postgraduate Program, Fortaleza, Brazil
2 Centro de Informação e Assistência Toxicológica do Instituto José Frota – IJF, Fortaleza, Brazil
3 Universidade de Fortaleza- UNIFOR, Medical Program, Fortaleza, Brazil (GRID:grid.412275.7) (ISNI:0000 0004 4687 5259)
4 Federal University of Ceará, Medical Sciences Postgraduate Program, Department of Internal Medicine, Medical School, Fortaleza, Brazil (GRID:grid.8395.7) (ISNI:0000 0001 2160 0329)
5 Federal University of Ceará, Pharmacology Postgraduate Program, Department of Physiology and Pharmacology, Medical School, Fortaleza, Brazil (GRID:grid.8395.7) (ISNI:0000 0001 2160 0329)
6 Federal University of Ceará, Clinical and Toxicological Analysis Department, School of Pharmacy, Fortaleza, Brazil (GRID:grid.8395.7) (ISNI:0000 0001 2160 0329)
7 Universidade de Fortaleza- UNIFOR, Medical Sciences Postgraduate Program, Fortaleza, Brazil (GRID:grid.412275.7) (ISNI:0000 0004 4687 5259); Universidade de Fortaleza-UNIFOR, Medical Course, Fortaleza, Brazil (GRID:grid.412275.7) (ISNI:0000 0004 4687 5259)