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Hypocitraturia: a risk factor for reduced bone mineral density in idiopathic hypercalciuria?
Maria-Goretti Moreira Guimarães Penido1, Eleonora Moreira Lima, Marcelo Ferraz Oliveira Souto
1Pediatric Nephrology Unit, GRIM, University Hospital, Federal University of Minas Gerais, Belo Horizonte, Brazil. mariagorettipenido@yahoo.com.br
Insights
Children with idiopathic hypercalciuria (IH) and hypocitraturia (HC) show lower bone density. This suggests an increased risk of osteopenia in these pediatric patients.
Area of Science:
- Pediatric Endocrinology
- Nephrology
- Bone Metabolism
Background:
- Idiopathic hypercalciuria (IH) is linked to reduced bone mineral density (BMD) in children.
- Hypocitraturia (HC) often co-occurs with IH, prompting investigation into its impact on bone health.
Purpose of the Study:
- To investigate the effect of hypocitraturia (HC) on the bone metabolism of children diagnosed with idiopathic hypercalciuria (IH).
Main Methods:
- Studied 88 children with IH, divided into groups with and without HC, plus a healthy control group.
- Measured urinary and blood electrolytes, urinary N-telopeptide, and bone mineral density (BMD) and bone mineral content (BMC) using dual energy X-ray absorptiometry.
Main Results:
- Children with IH and HC exhibited lower weight, height, BMI, and bone age, with higher serum intact parathyroid hormone (iPTH).
- Lumbar spine and femoral neck BMD and BMC were significantly lower in children with IH and HC compared to those without HC and controls.
- Height-adjusted bone mineral content (BMC) was lower in the IH with HC group.
Conclusions:
- Pediatric patients with idiopathic hypercalciuria (IH) and associated hypocitraturia (HC) may face a heightened risk of bone mass reduction and osteopenia.
- Further research is warranted to elucidate the specific role of hypocitraturia in pediatric bone disease associated with IH.
Unlabelled:
The association between idiopathic hypercalciuria (IH) and reduced bone mineral density (BMD) has been described in adults and children. Frequently, hypocitraturia (HC) is an associated condition. To determine the effect that HC may have on bone metabolism of these patients, we studied 88 children with IH at diagnosis, divided into the following groups: group 1-44 (50%) patients with associated HC; group 2-44 (50%) patients without HC; group 3 (29 subjects), a healthy control group. Urinary and blood electrolytes, as long as urinary N-telopeptide, were measured. Lumbar spine (L2-L4) and femoral neck bone mineral density (BMD) and bone mineral content (BMC) were measured by dual energy X-ray absorptiometry. There was no difference in age between the three groups (P=0.80), but weight, height, body mass index, and bone age were lower (P<0.01) and serum intact parathyroid hormone (iPTH) was higher (P<0.05) in group 1 than in groups 2 and 3. N-telopeptide, measured in urine, did not differ between groups. The following bone densitometry parameters: lumbar spine BMC, BMC adjusted for height (BMCh), BMC adjusted for width of vertebrae (BMCw) and BMD, as well as femoral neck BMD, were significantly lower in group 1 than in groups 2 and 3 (P<0.01). When we corrected densitometry parameters for height, BMC was lower in group 1 and not in group 2 when compared with controls.
Conclusions:
Children with IH and associated HC may have a higher risk of bone mass loss and consequent osteopenia. Further studies are needed to assess the role that hypocitraturia may have in this form of bone disease.
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