Lower-leg growth rates in children with asthma during treatment with ciclesonide and fluticasone propionate

Lone Agertoft1, Søren Pedersen

  • 1Pediatric Research Unit, Kolding Hospital, University of Southern Denmark, Kolding, Denmark. lone_agertoft@dadlnet.dk

Insights

Ciclesonide (CIC) did not affect children's lower-leg growth, unlike fluticasone propionate (FP). FP significantly reduced growth rate compared to placebo and CIC in mild asthma patients.

Area of Science:

  • Pediatric Endocrinology
  • Respiratory Medicine
  • Pharmacology

Background:

  • Inhaled corticosteroids (ICS) are standard therapy for pediatric asthma.
  • Assessing systemic effects of ICS, particularly on growth, is crucial.
  • Knemometry is an established method for measuring short-term lower-leg growth rate in children.

Purpose of the Study:

  • To compare the effects of ciclesonide (CIC) and fluticasone propionate (FP) on lower-leg growth rate.
  • To evaluate the impact of CIC and FP on hypothalamic-pituitary-adrenal-axis function in children with mild asthma.

Main Methods:

  • A double-blind, placebo-controlled, three-period crossover study.
  • 28 children (aged 6-12 years) received daily doses of CIC 320 μg, FP 375 μg, or placebo via a spacer.
  • Knemometry measured lower-leg growth; 12-h overnight urine cortisol levels assessed adrenal function.

Main Results:

  • Ciclesonide (CIC) showed no statistically significant difference in lower-leg growth rate compared to placebo.
  • Fluticasone propionate (FP) significantly reduced lower-leg growth rate versus placebo (p=0.0002) and CIC (p=0.0137).
  • Overnight urine cortisol was significantly lower with FP than CIC (p<0.05), but no significant differences were found versus placebo.

Conclusions:

  • Ciclesonide (CIC) demonstrated no significant impact on lower-leg growth in children with mild asthma.
  • Fluticasone propionate (FP) at the tested dose significantly inhibited lower-leg growth compared to both placebo and CIC.
  • These findings highlight potential differences in systemic growth effects between ICS medications.

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