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Case-control study demonstrates elevated serum and urinary interleukin-15 levels in pediatric cystic kidney disease, indicating early inflammatory signaling independent of renal function.
Cystic kidney disease is characterized by progressive structural remodeling of renal parenchyma and altered cellular signaling. Inflammatory mediators may contribute to disease biology; however, data on interleukin-15 (IL-15) in pediatric cystic kidney disorders remain limited. The aim of this study was to assess serum and urinary IL-15 concentrations in children with cystic kidney disease and to evaluate their association with renal function. Methods: This study included 47 children with cystic kidney disease and 41 controls without renal cystic disease or other systemic, inflammatory, or immunological disorders. Serum and urinary IL-15 concentrations were measured using an enzyme-linked immunosorbent assay (ELISA). Renal function was assessed using the estimated glomerular filtration rate (eGFR). Statistical analyses included non-parametric comparisons, logistic regression, and receiver operating characteristic (ROC) curve analysis. Results: Children with cystic kidney disease demonstrated significantly elevated serum and urinary IL-15 concentrations compared with controls. IL-15 levels were not associated with eGFR and did not differ between cystic disease subtypes. In logistic regression analysis, IL-15 remained significantly associated with disease status. ROC analysis suggested high diagnostic ability of serum and urinary IL-15. Conclusions: IL-15 concentrations are increased in children with cystic kidney disease independently of current renal function. These findings suggest that IL-15 may reflect early inflammatory or epithelial signaling rather than established functional impairment.
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Bogdał et al. (2026) studied this question.
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