Pharmacokinetics of buspirone in autistic children

J Clin Pharmacol. 2006 May;46(5):508-14. doi: 10.1177/0091270006286903.

Abstract

Buspirone is used to treat generalized anxiety disorder in children and may be useful in developmental disorders in which brain serotonin synthesis is altered. Autistic children (13 boys, 7 girls) were given a single oral dose of 2.5 mg (2-3 years) or 5.0 mg (4-6 years). Blood was collected for 8 hours, and plasma was assayed for buspirone and its metabolite 1-pyrimidinylpiperazine (1-PP). The peak concentration of buspirone averaged 1141 +/- 748 pg/mL with a time to maximum concentration of 0.8 hours. Half-life was 1.6 +/- 0.3 hours. Peak concentrations of 1-PP were 4.5-fold higher than for buspirone. Girls had higher peak concentrations (1876 vs 746 pg/mL) for buspirone and a lower peak 1-PP/buspirone concentration ratio. These results suggest that buspirone is rapidly absorbed and eliminated in young children with extensive metabolism to 1-PP. Plasma concentrations with 2.5- to 5.0-mg doses were similar to those observed in older children receiving 7.5- to 15-mg doses.

Publication types

  • Clinical Trial
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Anxiety Agents / blood
  • Anti-Anxiety Agents / pharmacokinetics*
  • Autistic Disorder / metabolism*
  • Buspirone / analogs & derivatives
  • Buspirone / blood
  • Buspirone / pharmacokinetics*
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Serotonin Receptor Agonists / blood
  • Serotonin Receptor Agonists / pharmacokinetics*

Substances

  • Anti-Anxiety Agents
  • Serotonin Receptor Agonists
  • 1-(2-pyrimidinyl)piperazine
  • Buspirone