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Hypervitaminosis A in Pediatric Patients With Advanced Chronic Kidney Disease
Meredith Harris1, Charles Varnell2, Veronica Taylor3
1Division of Nephrology & Hypertension, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Insights
Hypervitaminosis A is common in advanced chronic kidney disease (CKD), linked to bone issues. Formula-fed children with CKD show higher vitamin A and altered bone health markers, necessitating monitoring.
Area of Science:
- Pediatric Nephrology
- Nutritional Science
- Bone Metabolism
Background:
- Hypervitaminosis A is recognized but often overlooked in chronic kidney disease (CKD).
- Elevated vitamin A levels are associated with hypercalcemia and mineral bone disease in CKD patients.
- Understanding vitamin A's impact on bone health in advanced CKD is crucial.
Purpose of the Study:
- To determine the prevalence of hypervitaminosis A in children with advanced CKD.
- To investigate the association between vitamin A levels and bone health indicators.
- To compare vitamin A and bone health markers between formula-fed and non-formula-fed CKD populations.
Main Methods:
- Retrospective review of 58 children with CKD stages 4-5.
- Analysis of vitamin A, calcium, and parathyroid hormone levels.
- Comparison between primarily formula-fed (FF) and non-primarily formula-fed (NFF) cohorts.
Main Results:
- 97% of patients (56/58) exhibited hypervitaminosis A.
- Formula-fed patients had significantly higher vitamin A levels (2.9x ULN) compared to non-formula-fed (2.2x ULN).
- Formula-fed group showed a trend towards higher calcium and a significant increase in lower-than-goal parathyroid hormone levels.
Conclusions:
- Formula feeding is associated with higher vitamin A and calcium levels in advanced CKD.
- Formula-fed children with CKD are at increased risk for adynamic bone disease due to lower PTH.
- Routine monitoring of vitamin A levels and dietary interventions are recommended for bone health in CKD.
Objective:
Hypervitaminosis A is well-described but overlooked in chronic kidney disease (CKD) and has been associated with hypercalcemia, contributing to mineral bone disease. Our objective is to assess prevalence of hypervitaminosis A and its association with bone health in an advanced-CKD population.
Methods:
We performed a retrospective review of 58 children with CKD 4-5 to examine the association between vitamin A levels and bone health and compared these values between a primarily formula-fed (FF) and nonprimarily formula-fed cohort (NFF).
Results:
Fifty-six of 58 patients (97%) had hypervitaminosis A with a mean vitamin A level of 1,475 ± 597 mcg/dL. When compared with the upper limit of normal vitamin A level for age, the FF group's vitamin A level was 2.9x upper limit of normal and the NFF group's vitamin A level was 2.2x upper limit of normal (P = .02). The mean calcium level was 10.3 mg/dL in the FF group and 9.8 mg/dL in the NFF group (P = .057). Percent of patients lower than, within, or greater than goal parathyroid hormone range was statistically significant with 15 (62%) of the FF group lower than goal and 16 (72%) of the NFF cohort greater than goal (P = .006).
Conclusions:
We concluded vitamin A and calcium levels are higher in the FF versus the NFF population. FF patients are more likely to have parathyroid hormone levels lower than the goal range, placing them at risk for adynamic bone disease. We recommend monitoring vitamin A levels as part of routine nutritional assessments and dietary interventions to prevent hypervitaminosis A to improve bone health in late CKD.
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