Document Type : Original Article
Authors
1
Pediatric Department, Faculty of Medicine, Benha University, Benha, Egypt
2
Clinical and Chemical Pathology, Faculty of Medicine, Benha University, Benha, Egypt
3
Pediatrics Department, Faculty of Medicine, Benha University, Benha, Egypt.
4
Pediatrics Department, Faculty of Medicine, Benha University, Benha, Egypt
5
Consultant of Pediatrics - Head of Pediatric Endocrinology Unit, Damanhur Teaching Hospital
Abstract
Background: Diabetic nephropathy (DN), a leading complication of type 1 diabetes mellitus (T1DM) in children, remains a major contributor to end-stage renal disease. Emerging evidence suggests that tubular injury, rather than glomerular damage alone, may initiate renal dysfunction. Fibroblast Growth Factor 23 (FGF23), a regulator of phosphate metabolism, has been implicated in early kidney injury. This study aimed to assess FGF23 as a potential early biomarker of renal impairment in children with T1DM.Methods: This cross-sectional study included 50 children with T1DM (duration >5 years). Clinical assessments and laboratory investigations including HbA1C, eGFR, albumin/creatinine ratio (ACR), and serum FGF23 levels were conducted. Early renal impairment was defined as ACR ≥30 mg/g. Results: Early renal impairment was identified in 44% of patients. Children with renal impairment had significantly higher FGF23 levels (76 ± 10 vs. 51 ± 11 pg/mL, P < 0.001), higher HbA1C (10.4 ± 2 vs. 9 ± 1.5%, P = 0.009), and lower eGFR (78.9 ± 11.7 vs. 94.1 ± 21.6 mL/min/1.73m², P = 0.003). FGF23 positively correlated with phosphorus, creatinine, and ACR, and inversely with eGFR. ROC analysis showed excellent diagnostic accuracy for FGF23 (AUC = 0.955; cutoff >67 pg/mL; sensitivity: 86.4%, specificity: 96.4%). Multivariate analysis revealed FGF23 (OR = 1.414, P = 0.02) and HbA1C (OR = 5.529, P = 0.046) as independent predictors of early renal impairment. Conclusion: Elevated serum FGF23 is significantly associated with early renal impairment in T1DM children and may serve as a promising early biomarker to guide timely intervention.
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