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Bone disease in pediatric idiopathic hypercalciuria
Maria Goretti Moreira Guimarães Penido1, Marcelo de Sousa Tavares
1Maria Goretti Moreira Guimarães Penido, Marcelo de Sousa Tavares, Department of Pediatrics, Pediatric Nephrology Unit, School of Medicine, Federal University of Minas Gerais, Belo Horizonte, Belo Horizonte, CEP 30130100, Minas Gerais, Brazil.
Idiopathic hypercalciuria (IH), a common cause of kidney stones, is linked to reduced bone mineral density (BMD) in children and adults. Understanding IH pathogenesis is crucial for preventing bone loss and fractures.
Area of Science:
- Nephrology
- Endocrinology
- Metabolic Bone Disease
Background:
- Idiopathic hypercalciuria (IH) is a primary metabolic risk factor for urolithiasis.
- IH affects all age groups and is associated with reduced bone mineral density (BMD).
- The complex pathogenesis involves calcium homeostasis interplay between gut, bone, and kidney, influenced by hormones.
Purpose of the Study:
- To review the pathogenesis of idiopathic hypercalciuria.
- To explore the consequences of IH on bone mass accrual and maintenance.
- To elucidate the mechanisms underlying bone loss in IH patients.
Main Methods:
- Literature review of studies on idiopathic hypercalciuria and bone mineral density.
- Analysis of hormonal regulation of calcium homeostasis.
- Examination of cellular transport of calcium in intestines, kidneys, and bones.
Main Results:
- IH is a systemic abnormality affecting calcium homeostasis.
- Reduced BMD is observed in pediatric and adult IH patients.
- Mechanisms of bone loss or impaired bone mass gain in IH remain unclear.
Conclusions:
- IH impacts bone health, potentially leading to reduced peak bone mass and increased fracture risk.
- Further research is needed to understand the precise mechanisms of bone loss in IH.
- Addressing IH may be critical for optimizing bone health throughout the lifespan.
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