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New Biomarker Panel Enhances Prediction of CKD Progression in Children

New Biomarker Panel Enhances Prediction of CKD Progression in Children

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A groundbreaking biomarker panel developed by Yale researchers improves the prediction of chronic kidney disease progression in children, supporting personalized care and better outcomes.

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Researchers from Yale School of Medicine have developed a novel biomarker panel that significantly improves the assessment of chronic kidney disease (CKD) progression in pediatric patients. Their study, published in the Journal of the American Society of Nephrology, analyzed over 500 children aged six months to sixteen years from the CKD in Children (CKiD) Cohort Study.

This biomarker panel utilizes measurements from plasma and urine to better predict which children are at higher risk of disease progression. It builds on previous research by the CKD Biomarkers Consortium, which examined indicators related to kidney tubule health, injury, and inflammation. The researchers employed advanced regression tree-based statistical modeling to identify the most informative predictors.

The key biomarkers identified include the urine albumin-to-creatinine ratio, the urine epidermal growth factor (EGF) to creatinine ratio, plasma kidney injury molecule-1 (KIM-1), and the estimated glomerular filtration rate (eGFR). Combining these markers allows clinicians to more accurately identify children at greatest risk of CKD advancing toward kidney failure, which can lead to dialysis or transplant.

"Current clinical biomarkers only partially capture the variability of CKD progression," said Dr. Jason Greenberg, lead author and associate professor at Yale. "This new biomarker panel, reflecting vital pathways of kidney health, can markedly enhance risk prediction." He emphasized that integrating tubular health biomarkers into risk assessment addresses an often-overlooked aspect of pediatric CKD.

The study's findings could help improve personalized monitoring and treatment strategies, potentially slowing disease progression and enhancing long-term outcomes for affected children. Dr. Greenberg highlighted that this advancement supports the translation of laboratory discoveries into practical clinical tools. Dr. F. Perry Wilson from Yale also noted that such predictive insights allow for better patient engagement and tailored care, ultimately demonstrating the promise of personalized medicine in pediatric nephrology.

This research provides a significant step forward in early identification and management of pediatric CKD, aiming to improve the quality of life and health outcomes for young patients.

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