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Breast milk-associated physiological hypercalcaemia: an observational study of clinical, biochemical and radiological
Sandhya Govindarajan1, Mohamed Zulf Mughal2, Imran Zamir3
1Manchester University NHS Foundation Trust, Manchester, UK ggsan28@gmail.com.
Insights
Physiological hypercalcaemia in breastfed infants is benign and resolves on its own. Infants can continue exclusive breastfeeding without intervention, as this condition does not cause symptoms or kidney issues.
Area of Science:
- Pediatric Endocrinology
- Neonatal Nutrition
- Infant Health
Background:
- Asymptomatic physiological hypercalcaemia is recognized in exclusively breastfed infants.
- Characterization of this condition during continued breastfeeding is limited.
Purpose of the Study:
- To evaluate clinical, biochemical, and radiological outcomes of breast milk-associated physiological hypercalcaemia.
- To assess the safety and impact of continued exclusive breastfeeding in affected infants.
Main Methods:
- A multi-center retrospective study over 5 years.
- Included exclusively breastfed infants with hypercalcaemia (serum corrected calcium [cCa] ≥2.8 mmol/L) and no other identified causes.
- Analyzed clinical, biochemical, and radiological data.
Main Results:
- Twenty-five infants with mean peak cCa of 3.08 mmol/L were studied.
- All infants were asymptomatic and continued exclusive breastfeeding without interventions.
- No nephrocalcinosis was observed on renal ultrasound; hypercalcaemia resolved spontaneously.
Conclusions:
- Breast milk-associated physiological hypercalcaemia is a benign, PTH-independent condition.
- Infants can safely continue exclusive breastfeeding without formula changes.
- Further research is needed to understand the underlying mechanisms.
Introduction:
Asymptomatic physiological hypercalcaemia in exclusively breastfed infants is recognised but has not been systematically characterised when breastfeeding is continued.
Objective:
To evaluate the clinical, biochemical and radiological outcomes of breast milk-associated physiological hypercalcaemia.
Methods:
A multi-centre retrospective study over 5 years included infants with hypercalcaemia (serum corrected calcium (cCa) ≥2.8 mmol/L) who were exclusively breastfed and had no other identifiable causes of hypercalcaemia. Clinical, biochemical and radiological data were analysed.
Results:
Twenty-five infants (15 males, 10 females) were studied. The mean peak cCa was 3.08 mmol/L (SD 0.17; normal 2.2-2.8 mmol/L). All infants were asymptomatic and continued exclusive breastfeeding without interventions such as intravenous fluids, diuretics or bisphosphonates. Mean serum parathyroid hormone (PTH) was suppressed at 1.04 pmol/L (SD 0.9; reference 2.0-9.4 pmol/L). Renal ultrasound examinations performed in all infants showed no nephrocalcinosis. Hypercalcaemia resolved spontaneously over a median of 64 (range, 9-329) days, and the median duration of exclusive breastfeeding was 150 (range, 8-540) days.
Conclusion:
Breast milk-associated physiological hypercalcaemia is a benign, PTH-independent condition without clinical symptoms or nephrocalcinosis. Infants can safely continue exclusive breastfeeding, preserving its well-established benefits, without switching to low calcium formulas. Further research is needed to elucidate the underlying mechanisms.
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