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Updated: Oct 13, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Fibroblast Growth Factor 23 Level and Cardiovascular Parameters in Children with Chronic Kidney Disease
Gaurav Singh1, Om P Mishra2, Abhishek Abhinay1
1Division of Pediatric Nephrology, Department of Pediatrics, Banaras Hindu University, Varanasi, Uttar Pradesh, 221005, India.
Insights
Serum fibroblast growth factor 23 (FGF-23) levels increase with chronic kidney disease (CKD) severity. However, FGF-23 did not correlate with cardiovascular abnormalities in pediatric CKD patients, with systolic blood pressure being a key risk factor for increased carotid intima-medial thickness.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Research
- Biomarkers in Chronic Disease
Background:
- Chronic kidney disease (CKD) in children is associated with cardiovascular complications.
- Fibroblast growth factor 23 (FGF-23) is a biomarker implicated in CKD progression and cardiovascular disease.
- Understanding the relationship between FGF-23 and cardiovascular parameters in pediatric CKD is crucial for risk stratification.
Purpose of the Study:
- To investigate serum FGF-23 levels across different CKD grades in children.
- To determine the prevalence of abnormal left ventricular mass index (LVMI), carotid intima-medial thickness (cIMT), and central pulse wave velocity (cPWV) in pediatric CKD.
- To identify risk factors, including FGF-23, associated with these cardiovascular abnormalities.
Main Methods:
- A cohort of 59 pediatric CKD patients (G2-G5) was studied.
- Measurements included serum intact FGF-23, LVMI, cIMT, and cPWV.
- Statistical analysis assessed correlations and risk factors for cardiovascular abnormalities.
Main Results:
- Serum FGF-23 levels were significantly elevated in all CKD grades compared to controls and increased with CKD severity.
- Abnormalities were prevalent: increased LVMI (71.2%), elevated cIMT (57.7%), and cPWV (26.9%).
- FGF-23 correlated negatively with eGFRcr and positively with iPTH, phosphate, and alkaline phosphatase, but not with LVMI, cIMT, or cPWV. Only systolic BP SDS predicted increased cIMT.
Conclusions:
- Serum FGF-23 levels rise with CKD progression in children but show no significant association with LVMI, cIMT, or cPWV.
- Systolic blood pressure is a significant risk factor for increased cIMT in pediatric CKD.
- Further research is needed to elucidate the role of FGF-23 in pediatric CKD cardiovascular complications.
Objective:
To find out the serum fibroblast growth factor 23 (FGF-23) levels in different grades of CKD, and the prevalence of abnormal left ventricular mass index (LVMI), carotid intima-medial thickness (cIMT), and central pulse wave velocity (cPWV) and the risk factors including FGF-23 for these abnormalities.
Methods:
Fifty-nine patients of CKD with G2 to G5, aged 2-18 y were included. The LVMI, cIMT, and cPWV were measured using standard techniques, and serum intact FGF-23 levels were estimated at enrollment.
Results:
Median FGF-23 levels were significantly raised in all the grades of CKD than controls (p < 0.001), and also in G4 and G5 in comparison to G2&3 and in G5D than G5. Increased LVMI in 42 (71.2%), elevated cIMT in 30 (57.7%), and cPWV in 14 (26.9%) patients were found. The FGF-23 showed significant negative correlation with eGFRcr and positive with serum iPTH, phosphate and alkaline phosphatase levels, but had no correlations with LVMI, cIMT SDS, and cPWV SDS. Only systolic BP SDS (odds ratio 1.5, 95% CI 1.008-2.231, p = 0.046) was observed as a significant predictor for increased cIMT, while no variables had any association with abnormal LVMI and cPWV.
Conclusions:
Serum FGF-23 showed higher levels with increasing grades of CKD, but no significant association with cardiovascular parameters. Systolic BP SDS was found as a significant risk factor for increased cIMT in children with CKD.
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