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[Phosphorus-calcium metabolism in children under prolonged treatment with anticonvulsants. (II)]

M J Peña Griñán1, M D Lluch Fernández, M J Montoya García

  • 1Departamento de Pediatría, Hospital Universitario Virgen Macarena, Sevilla.

Insights

Anticonvulsant drugs like phenobarbital and polytherapy significantly reduce 25-Hydroxycholecalciferol levels in children. Alkaline phosphatase increased with phenobarbital, carbamazepine, and polytherapy, impacting phosphocalcium metabolism.

Area of Science:

  • Pediatric Endocrinology
  • Clinical Biochemistry
  • Pharmacology

Background:

  • Anticonvulsant drugs are widely used in children for epilepsy management.
  • Prolonged use of certain anticonvulsants may affect bone metabolism.
  • Phosphocalcium metabolism is crucial for skeletal health in growing children.

Purpose of the Study:

  • To compare the effects of different anticonvulsant drugs on phosphocalcium metabolism in children.
  • To assess biochemical parameters including 25-Hydroxycholecalciferol, alkaline phosphatase, calcium, parathyroid hormone, and osteocalcin.
  • To investigate the influence of treatment duration on these metabolic parameters.

Main Methods:

  • Comparative biochemical analysis in 98 children aged 1-14 years.
  • Assessment of 25-Hydroxycholecalciferol, alkaline phosphatase, calcium, parathyroid hormone, and osteocalcin levels.
  • Group comparisons included phenobarbital, carbamazepine, valproate, polytherapy, and a control group.

Main Results:

  • Phenobarbital and polytherapy significantly decreased 25-Hydroxycholecalciferol levels (p=0.0001).
  • Alkaline phosphatase was significantly higher in children on phenobarbital, carbamazepine, and polytherapy (p<0.05).
  • No significant differences were observed for calcium, parathyroid hormone, or osteocalcin levels across groups or with duration.

Conclusions:

  • Phenobarbital and polytherapy demonstrate the most significant impact on 25-Hydroxycholecalciferol levels in pediatric patients.
  • Elevated alkaline phosphatase suggests potential bone turnover alterations with certain anticonvulsants.
  • Long-term anticonvulsant therapy requires monitoring of vitamin D status and bone metabolism markers.

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