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Fibroblast growth factor 23 and left ventricular hypertrophy in dialyzed versus nondialyzed children with chronic
Nagwan Yossery Saleh1, Fahima Mohammed Hassan1, Mona Salah Habib2
1Department of Pediatrics, Faculty of Medicine, Menoufia University, Shibin Al Kawm, Egypt.
Insights
Fibroblast growth factor 23 (FGF23) is elevated in children with chronic kidney disease (CKD) undergoing dialysis. Higher FGF23 levels correlate with left ventricular hypertrophy (LVH) in these pediatric CKD patients.
Area of Science:
- Biochemistry
- Pediatric Nephrology
- Cardiology
Background:
- Fibroblast growth factor 23 (FGF23) is integral to phosphate and Vitamin D metabolism.
- Elevated FGF23 is linked to left ventricular hypertrophy (LVH) and mortality in chronic kidney disease (CKD).
- FGF23's role in LVH assessment among pediatric CKD patients, particularly dialyzed versus nondialyzed, requires further evaluation.
Purpose of the Study:
- To investigate the association between FGF23 levels and LVH in children with CKD.
- To compare FGF23 levels in pediatric CKD patients undergoing hemodialysis versus those not on dialysis.
Main Methods:
- A prospective observational study included 50 children with CKD, divided into hemodialysis (n=34) and nondialysis (n=16) groups.
- Serum levels of creatinine, calcium, phosphorus, and FGF23 were measured.
- Echocardiography was performed to assess cardiac parameters, including left ventricular mass (LVM), LVM index (LVMI), and relative wall thickness (RWT).
Main Results:
- Serum FGF23 levels were significantly higher in dialyzed pediatric CKD patients compared to nondialyzed patients.
- FGF23 levels showed a significant positive correlation with dialysis duration and serum phosphorus.
- Positive correlations were observed between FGF23 and LVM, LVMI, and RWT, indicating an association with LVH.
Conclusions:
- Serum FGF23 levels are significantly elevated in dialyzed children with CKD.
- FGF23 levels correlate with serum phosphorus, supporting its role in phosphate homeostasis.
- FGF23 is a valuable marker for assessing LVH in pediatric CKD patients, particularly those on dialysis.
Background:
Fibroblast growth factor 23 (FGF23) is a protein encoded by the FGF23 gene in humans. It belongs to the FGF family, which plays a crucial role in phosphate and Vitamin D metabolism. The primary function of FGF23 appears to be regulating phosphate levels in plasma. Elevated FGF23 levels are consistently linked to left ventricular hypertrophy (LVH) and are a major risk factor for mortality in chronic kidney disease (CKD). We aimed to evaluate the role of FGF23 in assessing the association with LVH in dialyzed versus nondialyzed children with CKD.
Patients And Methods:
This prospective observational study involved 50 children with CKD divided into two groups: Group I consisted of 34 subjects undergoing regular hemodialysis, whereas Group II included 16 subjects not on hemodialysis. Various tests were done, including serum creatinine, calcium, phosphorus, and FGF23, along with echocardiography.
Results:
There was a statistically significant increase in FGF23 levels in dialyzed compared to nondialyzed patients. A significant positive correlation was found between serum FGF-23 levels and the duration of dialysis and serum phosphorus. In addition, a positive correlation was observed between FGF23 and left ventricular mass (LVM), LVM index (LVMI), and relative wall thickness (RWT). The area under the curve of FGF23 for identifying LVH was 0.803, with a sensitivity of 85.7% and specificity of 63.9%.
Conclusions:
Serum FGF-23 levels were significantly increased in dialyzed children compared to nondialyzed children. FGF-23 levels were significantly correlated with serum phosphorus levels, confirming the role of FGF23 in phosphate homeostasis. In addition, there were significant positive correlations between FGF23 levels and LVM, LVMI, and RWT, reinforcing FGF23's role in assessing the association with LVH.
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