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Updated: Jun 25, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Vitamin D deficiency in children with chronic kidney disease: uncovering an epidemic
Farah N Ali1, Lester M Arguelles, Craig B Langman
1Feinberg School of Medicine, Northwestern University, Children's Memorial Hospital, 2300 Children's Plaza, Box 37, Chicago, IL 60614, USA.
Insights
Children with chronic kidney disease (CKD) have a high risk of vitamin D deficiency, with prevalence increasing over time. This deficiency impacts bone health and varies by ethnicity and season.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Bone Metabolism
Background:
- Vitamin D deficiency impairs bone mineralization in children.
- Children with chronic kidney disease (CKD) face risks of renal osteodystrophy and vitamin D deficiency.
- Current guidelines recommend 25-hydroxyvitamin D (25[OH]D) measurement in CKD stages 2+ with elevated parathyroid hormone, but prevalence data are limited.
Purpose of the Study:
- To determine vitamin D deficiency prevalence in pediatric CKD.
- To evaluate changes in vitamin D deficiency over time.
- To examine ethnic and seasonal variations in 25[OH]D levels.
Main Methods:
- Measured 25[OH]D levels in pediatric CKD patients (stages 1-5) from 1987-1996 and 2005-2006.
- Analyzed trends in 25[OH]D levels over a decade.
- Assessed seasonal and ethnic differences in 25[OH]D.
Main Results:
- Vitamin D deficiency prevalence ranged from 20% to 75% during the 1987-1996 decade.
- A significant decreasing trend in 25[OH]D levels was observed over the decade.
- In 2005-2006, 39% of pediatric CKD patients had vitamin D deficiency (mean 25[OH]D: 21.8 ng/mL), with lower levels in Black and Hispanic children.
Conclusions:
- Pediatric CKD patients are at high risk for vitamin D deficiency, with increasing prevalence noted.
- Vitamin D deficiency remains a significant issue in contemporary pediatric CKD populations.
- Sunlight exposure and ethnicity influence 25[OH]D levels, supporting current guidelines for monitoring in CKD.
Background:
Vitamin D deficiency in children adversely affects bone development by reducing mineralization. Children with chronic kidney disease are at risk for altered bone development from renal osteodystrophy and concomitant vitamin D deficiency. The pediatric Kidney Disease Outcomes Quality Initiative guidelines suggest measuring serum 25-hydroxyvitamin D (25[OH]D) levels if serum parathyroid hormone levels are above the target range for chronic kidney disease stages 2 and beyond, but the magnitude of vitamin D deficiency in children with chronic kidney disease is not well studied.
Objectives:
The purpose of this work was to determine whether children with chronic kidney disease had vitamin D deficiency, to evaluate whether the prevalence of vitamin D deficiency changed over time, and to examine seasonal and ethnic differences in 25(OH)D levels.
Methods:
25(OH)D levels in children with chronic kidney disease (stages 1-5) were measured over a 10-year period from 1987 to 1996. Data were also collected for a contemporary group of patients from 2005 to 2006. RESULTS. The prevalence of vitamin D deficiency ranged from 20% to 75% in the decade studied. There was a significant trend for decreasing 25(OH)D levels over the decade, both at the group and individual levels. Seasonal variation was noted. In our contemporary population with chronic kidney disease, the mean 25(OH)D level was 21.8 ng/mL; we found a prevalence of vitamin D deficiency of 39%. Black and Hispanic patients had lower levels of 25(OH)D than white patients.
Conclusions:
Children with chronic kidney disease have great risk for vitamin D deficiency, and its prevalence was increasing yearly in the studied decade. Contemporary data show that vitamin D deficiency remains a problem in these children. Sunlight exposure and ethnicity play a role in levels of 25(OH)D. Our data support the recent pediatric Kidney Disease Outcomes Quality Initiative guidelines for measurement of 25(OH)D levels in children with chronic kidney disease and secondary hyperparathyroidism.
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