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Updated: Jan 29, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Early predictors of cardiac dysfunction in Egyptian children with chronic kidney disease
Mohamed Abdelaziz El-Gamasy1, Walid Ahmed El-Shehaby1, Maaly M Mabrouk2
1Department of Pediatrics, Faculty of Medicine, Tanta University, Tanta, Egypt.
Insights
In children with chronic kidney disease (CKD), high phosphorus and calcium-phosphorus product levels predict early diastolic dysfunction and increased left ventricular mass. Vitamin D deficiency was not directly linked to these cardiac issues in this study.
Area of Science:
- Pediatric Nephrology
- Cardiology
- Mineral Bone Disorder
Background:
- Cardiovascular morbidity is a leading cause of mortality in pediatric chronic kidney disease (CKD).
- Diastolic cardiac dysfunction and increased left ventricular mass (LVM) are key risk factors in these patients.
- Vitamin D deficiency has been implicated as a risk factor for cardiovascular complications in CKD.
Purpose of the Study:
- To investigate the relationship between mineral bone disorder biomarkers (serum 25(OH) Vitamin D3, phosphorus, Ca×Po4 product) and cardiac function (diastolic function, LVM) in pediatric CKD patients.
- To assess the prognostic value of these biomarkers for cardiac abnormalities.
Main Methods:
- Cross-sectional observational study involving 86 pediatric CKD patients (stages 4-5) and 40 healthy controls.
- Assessment of serum 25(OH) Vitamin D3, phosphorus, calcium-phosphorus product, and intact parathyroid hormone (iPTH).
- Evaluation of diastolic function and LVM using Doppler echocardiography, tissue Doppler imaging, and M-mode echocardiography.
Main Results:
- Pediatric CKD patients exhibited significantly lower serum 25(OH) Vitamin D3 levels compared to controls.
- Diastolic dysfunction was observed in 48.8% of CKD patients and was associated with elevated serum phosphorus and Ca×Po4 product.
- Increased LVM showed a significant positive correlation with iPTH levels.
Conclusions:
- Hyperphosphatemia and a high calcium-phosphorus product are valuable predictors of early diastolic dysfunction and increased LVM in children with CKD.
- These findings highlight the importance of managing mineral and bone disorders to mitigate cardiovascular risks in pediatric CKD.
Background:
Cardiovascular morbidity (CVM) is the main etiology of mortality in children and adolescents with chronic kidney disease (CKD). CKD associated cardiovascular mortality is more common in children with diastolic cardiac dysfunction which was considered as an early indicator for death, while increased left ventricular mass (LVM) is a strong independent risk factor for these patients. Vitamin D deficiency was previously studied as one of the risk factors for CVM.
Aim:
The aim of the work was to investigate the relationship between biomarkers of mineral bone disorder including serum 25(OH) Vitamin D3 (25-OH D3), phosphorus and calcium × phosphorus (Ca×Po4) product with diastolic cardiac function and LVM in children and adolescents with CKD.
Subjects And Methods:
This was a cross-sectional observational study. Participants were classified into two groups: Group I including 86 pediatric patients with CKD (stages 4 or 5) and Group II including 40 healthy controls. Group I was subdivided into IA included children with diastolic dysfunction and IB included cases without diastolic dysfunction. 25-OH D3 level was measured by enhanced chemiluminescence method and intact parathyroid hormone (iPTH) by electrochemiluminescence method. Parameters for diastolic function and LVM were assessed by Doppler echocardiography, tissue Doppler imaging, and M-mode echocardiography.
Results:
25-OH D3 level was significantly lower in Group I when compared to Group II. Diastolic dysfunction was present in 48.8% of the studied patients and was significantly associated with increased serum phosphorus and calcium-phosphorus product but not with decreased level of 25-OH D3. There was a significant positive correlation between LVM and iPTH.
Conclusions:
Hyperphosphatemia and high Ca×Po4 product were considered of prognostic value as they predict early diastolic dysfunction and increased LVM in children with CKD.
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