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Updated: May 29, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Vitamin D deficiency and arterial wall stiffness in children with chronic kidney disease
Amit R Patange1, Rudolph P Valentini, Wei Du
1Carmen and Ann Adams Department of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit, MI, USA. apatange@med.wayne.edu
Insights
Nutritional vitamin D deficiency is linked to arterial wall stiffness in children with chronic kidney disease (CKD). Low vitamin D levels independently predict increased arterial stiffness in pediatric CKD patients on hemodialysis.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Complications in CKD
- Vascular Biology
Background:
- Arterial wall stiffness is a known complication in pediatric chronic kidney disease (CKD), often preceding cardiac issues.
- The exact causes of vascular abnormalities in children with CKD remain unclear.
- Understanding these vascular changes is crucial for managing long-term health outcomes.
Purpose of the Study:
- To investigate the relationship between calcium-phosphorus metabolism, including 25-hydroxy vitamin D, and arterial wall stiffness in pediatric CKD patients.
- To identify potential predictors of arterial stiffness in this vulnerable population.
- To explore the role of nutritional status in vascular health among children with CKD.
Main Methods:
- A cohort of 43 pediatric CKD patients without prior cardiac disease was studied.
- Arterial stiffness was assessed using the Augmentation Index (AI) via radial artery tonometry.
- Serum markers of calcium-phosphorus metabolism, including 25-hydroxy vitamin D, were measured concurrently.
Main Results:
- Arterial stiffness (AI) correlated with declining kidney function.
- Low serum 25-hydroxy vitamin D levels were observed and negatively correlated with AI.
- 25-hydroxy vitamin D was the sole independent predictor of arterial stiffness in children on hemodialysis.
Conclusions:
- This study suggests a significant association between vitamin D deficiency and increased arterial stiffness in pediatric CKD patients.
- Nutritional vitamin D deficiency may be a key factor contributing to vascular complications in children with CKD.
- Further research into the mechanisms of vitamin D in regulating arterial stiffness is warranted for pediatric CKD management.
Abstract:
Arterial wall stiffness is a recognized complication in children with chronic kidney disease (CKD). Vascular abnormalities in these patients are shown to predate cardiac abnormalities such as left ventricular hypertrophy and diastolic dysfunction. The etiology of vascular abnormalities in these patients currently is not clear. This study explored the relationship between various parameters of calcium-phosphorus metabolism including 25-hydroxy vitamin D and arterial wall stiffness in pediatric patients with CKD. This study investigated a cohort of 43 children with CKD who had no history of underlying congenital or structural cardiac disease. The Augmentation Index (AI), a measure of peripheral arterial reflective properties using radial artery tonometry, was used as an indirect measure of central aortic stiffness. Serum biochemical markers of calcium-phosphorus metabolism were simultaneously measured. Univariate testing showed that AI correlated with worsening kidney function. Serum 25-hydroxy vitamin D levels were low and correlated negatively with AI (r = -0.39; p < 0.05). Multiple regression analysis showed that 25-hydroxy vitamin D was the only significant independent predictor of increased central arterial stiffness in the subgroup of children receiving hemodialysis. No association was observed between AI and any other measured biochemical parameter of calcium-phosphorus metabolism. This is the first study to investigate pediatric patients with CKD that suggests an association between nutritional vitamin D deficiency and increased arterial stiffness in children with CKD. The pathophysiologic mechanisms of vitamin D that regulate increased arterial stiffness need to be integrated further in pediatric CKD patients.
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