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Does idiopathic hypercalciuria affect bone metabolism during childhood? A prospective case-control study
Maria Pavlou1, Vasileios Giapros2, Anna Challa1
1Department of Pediatrics, University Hospital of Ioannina, Stavros Niarchos Avenue, 45500, Ioannina, Greece.
Insights
Idiopathic hypercalciuria in children shows normal bone formation but increased bone resorption. Dietary changes may help reduce bone resorption markers.
Area of Science:
- Pediatric Nephrology
- Pediatric Endocrinology
- Bone Metabolism
Background:
- Idiopathic hypercalciuria (IH) in children lacks extensive research on bone metabolism markers.
- Adult IH is associated with osteopenia, suggesting potential bone health implications in children.
- The osteoprotegerin (OPG) and soluble receptor activator of nuclear factor kB ligand (sRANKL) system's role in pediatric IH is understudied.
Purpose of the Study:
- To investigate biochemical markers of bone formation and resorption in children with IH.
- To evaluate the OPG/sRANKL system in children with IH.
- To assess the impact of a 3-month dietary intervention on these markers.
Main Methods:
- Prospective study of 50 children with IH and 50 healthy controls.
- Measurement of bone formation markers (total ALP, osteocalcin), bone resorption markers (β-Crosslaps), and OPG/sRANKL levels.
- Dietary recommendations for IH followed for 3 months, with pre- and post-intervention measurements.
Main Results:
- No significant differences in bone formation markers or OPG/sRANKL between groups.
- Children with IH exhibited higher β-Crosslaps and β-Crosslaps/osteocalcin ratio at diagnosis.
- A trend towards decreased β-Crosslaps and reduced 24-h urinary calcium was observed after dietary intervention.
Conclusions:
- Pediatric IH is associated with normal bone formation but elevated bone resorption.
- Dietary intervention shows a potential beneficial effect on reducing bone resorption markers.
- Further research is warranted to understand long-term bone health in children with IH.
Background:
A limited number of studies have evaluated biochemical bone metabolism markers in children with idiopathic hypercalciuria, which in adults has been linked with osteopenia. Our aim was to investigate in children with idiopathic hypercalciuria biochemical markers of bone formation and resorption and the osteoprotegerin (OPG) and soluble receptor activator of nuclear factor kB ligand (sRANKL) system which is involved in the osteoclastogenesis process.
Methods:
A prospective study was conducted on 50 children with idiopathic hypercalciuria and 50 healthy age-, sex-, and Tanner stage-matched control subjects. Following the diagnosis, patients were requested to follow a 3-month dietary recommendation for idiopathic hypercalciuria. In patients, at diagnosis and at 3 months of follow-up, and in controls, bone-related hormones and serum/urine biochemical parameters were studied. The bone formation markers (total ALP and osteocalcin) and the bone resorption markers (β-Crosslaps) and the OPG and sRANKL levels were determined.
Results:
No differences were found in the bone formation markers or OPG and sRANKL between the children with idiopathic hypercalciuria and controls. The β-Crosslaps and the β-Crosslaps/osteocalcin ratio were higher in the patients at diagnosis than in controls (p = 0.019 and p = 0.029, respectively), with a trend to decrease after the 3-month dietary intervention. The initially increased 24-h urinary Ca in the patients decreased after the 3-month dietary intervention (p = 0.002).
Conclusions:
Children with idiopathic hypercalciuria had biochemical markers compatible with normal bone formation but increased bone resorption. After a 3-month dietary intervention, the trend observed towards decrease in the serum β-Crosslaps may reflect a beneficial response.
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