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Vitamin D and Calcium Homeostasis in Infants with Urolithiasis
Agnieszka Szmigielska1, Małgorzata Pańczyk-Tomaszewska2, Małgorzata Borowiec3
1Department of Pediatrics and Nephrology, Warsaw Medical University, Warsaw, Poland. aszmigielska@wum.edu.pl.
Insights
Infant urolithiasis is more common in boys, often linked to milk formula and vitamin D supplements. Key findings include hypercalcemia, hyperphosphatemia, and hypercalciuria in affected infants.
Area of Science:
- Pediatric Nephrology
- Infant Health
- Urolithiasis Research
Background:
- The incidence of urolithiasis (kidney stones) in infants remains largely unknown.
- Infantile urolithiasis presents unique diagnostic and management challenges.
- Understanding risk factors and metabolic profiles is crucial for early intervention.
Purpose of the Study:
- To investigate the clinical characteristics of urolithiasis in infants.
- To analyze nutritional factors, including milk formula and vitamin D supplementation.
- To assess serum and urinary levels of calcium, phosphate, 25-hydroxyvitamin D (25(OH)D), alkaline phosphatase, and parathyroid hormone.
Main Methods:
- Retrospective analysis of 32 infants diagnosed with urolithiasis (2-12 months old).
- Evaluation of clinical symptoms, feeding history (breastfed, formula-fed, mixed), and family history.
- Biochemical analysis of serum and urine for calcium, phosphate, 25(OH)D, alkaline phosphatase, and parathyroid hormone levels.
Main Results:
- Urolithiasis was more prevalent in boys (23 vs. 9 girls), who were also younger at diagnosis.
- Common symptoms included irritability (59%) and urinary tract infections (19%).
- Elevated serum calcium (94%) and phosphate (60%) were frequent. Hypercalciuria and hyperphosphaturia were observed in 34% and 25% of infants, respectively. Vitamin D supplementation and milk formula feeding were common.
Conclusions:
- Infantile urolithiasis appears more common in boys, particularly those fed milk formula with vitamin D supplementation.
- Metabolic abnormalities such as hypercalcemia, hyperphosphatemia, and hypercalciuria are prevalent in this population.
- Further research is needed to elucidate the precise mechanisms and long-term implications of urolithiasis in infancy.
Abstract:
The incidence of urolithiasis in infants is unknown. The aim of this study was to investigate clinical characteristics, nutrition, calcium, phosphate, 25-hydroxyvitamin D (25(OH)D), alkaline phosphate, and parathyroid hormone in infants with urolithiasis. There were 32 infants (23 boys and 9 girls) of the mean age of 6.4 ± 3.7 months (range 2-12 months), with diagnosis of urolithiasis enrolled into the study. Boys were younger than girls (5.3 vs. 9.1 months, respectively; p < 0.05). The infants were receiving prophylactic vitamin D3. Twenty-one of them were fed with milk formula, 9 were breastfed, and 2 were on a mixed diet. The major clinical symptoms consisted of irritability in 19 (59%) and urinary tract infection in 6 (19%) infants. Hypercalcemia and hyperphosphatemia were detected in the serum in 30 (94%) and 19 (60%) infants, respectively. The serum calcium level was higher in boys than girls (10.8 vs. 9.8 mg/dL, respectively; p < 0.05). Four (12.5%) infants had increased activity of alkaline phosphatase. The serum level of 25(OH)D was high in 3 (9%), low in 2 (6%), and normal in 27 (85%) infants. Parathyroid hormone was low in eight (25%) infants. Hypercalciuria and hyperphosphaturia were found in 11 (34%) boys and 8 (25%) girls. Family history of urolithiasis was positive in eight (25%) infants. We conclude that urolithiasis occurs in infancy more often in boys fed with milk formula and in those who received vitamin D supplementation. Hypercalcemia, hyperphosphatemia, and hypercalciuria are the most common changes present in clinical metabolic tests.
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