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Urinary L-FABP as an Early Biomarker for Pediatric Acute Kidney Injury Following Cardiac Surgery with Cardiopulmonary
Bruno Wilnes1, Beatriz Castello-Branco1, Bárbara Castello Branco1
1Interdisciplinary Laboratory of Medical Investigation, Unit of Pediatric Nephrology, Department of Pediatrics, Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte 30130-100, MG, Brazil.
Insights
Urinary liver-type fatty acid binding protein (uL-FABP) can help diagnose acute kidney injury (AKI) after pediatric cardiopulmonary bypass (CPB) earlier than current methods. Higher uL-FABP levels correlate with worse outcomes and may predict CPB-AKI development.
Area of Science:
- Nephrology
- Pediatric Surgery
- Biomarker Research
Background:
- Acute kidney injury (AKI) is a common complication following pediatric surgery involving cardiopulmonary bypass (CPB).
- Current diagnostic methods for CPB-AKI may not provide sufficiently early detection.
- Urinary liver-type fatty acid binding protein (uL-FABP) is a potential biomarker for kidney injury.
Conclusions:
- Elevated uL-FABP levels are associated with worse clinical outcomes in pediatric CPB-AKI.
- uL-FABP demonstrates potential as an early diagnostic and predictive biomarker for CPB-AKI in children.
- This biomarker may facilitate timely intervention and improved patient management.
Abstract:
Acute kidney injury (AKI) following surgery with cardiopulmonary bypass (CPB-AKI) is common in pediatrics. Urinary liver-type fatty acid binding protein (uL-FABP) increases in some kidney diseases and may indicate CPB-AKI earlier than current methods. The aim of this systematic review with meta-analysis was to evaluate the potential role of uL-FABP in the early diagnosis and prediction of CPB-AKI. Databases Pubmed/MEDLINE, Scopus, and Web of Science were searched on 12 November 2023, using the MeSH terms "Children", "CPB", "L-FABP", and "Acute Kidney Injury". Included papers were revised. AUC values from similar studies were pooled by meta-analysis, performed using random- and fixed-effect models, with p < 0.05. Of 508 studies assessed, nine were included, comprising 1658 children, of whom 561 (33.8%) developed CPB-AKI. Significantly higher uL-FABP levels in AKI versus non-AKI patients first manifested at baseline to 6 h post-CPB. At 6 h, uL-FABP correlated with CPB duration (r = 0.498, p = 0.036), postoperative serum creatinine (r = 0.567, p < 0.010), and length of hospital stay (r = 0.722, p < 0.0001). Importantly, uL-FABP at baseline (AUC = 0.77, 95% CI: 0.64-0.89, n = 365), 2 h (AUC = 0.71, 95% CI: 0.52-0.90, n = 509), and 6 h (AUC = 0.76, 95% CI: 0.72-0.80, n = 509) diagnosed CPB-AKI earlier. Hence, higher uL-FABP levels associate with worse clinical parameters and may diagnose and predict CPB-AKI earlier.
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