A randomized, placebo-controlled trial of effects of dexamethasone on hypothalamic-pituitary-adrenal axis in preterm

D M Wilson1, R B Baldwin, R L Ariagno

  • 1Department of Pediatrics, Stanford University, California 94305.

Insights

Seven days of dexamethasone therapy in preterm infants with bronchopulmonary dysplasia temporarily suppressed the hypothalamic-pituitary-adrenal axis and reduced weight gain. These effects were short-lived and resolved within 10 days post-treatment.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Neonatology

Background:

  • Bronchopulmonary dysplasia (BPD) is a chronic lung disease in preterm infants.
  • Glucocorticoid therapy is used for BPD, but its effects on the infant endocrine system require investigation.

Purpose of the Study:

  • To evaluate the impact of short-term, high-dose dexamethasone on the hypothalamic-pituitary-adrenal (HPA) axis in preterm infants with BPD.
  • To assess the effect of this therapy on infant weight gain.

Main Methods:

  • A blinded, randomized, placebo-controlled study involving 27 preterm infants with BPD.
  • Measurement of basal and adrenocorticotropic hormone (ACTH)-stimulated cortisol levels before, immediately after, and 10 days after 7 days of dexamethasone or placebo therapy.
  • Monitoring of infant weight gain during and after treatment.

Main Results:

  • Dexamethasone therapy significantly decreased basal and peak cortisol concentrations immediately post-treatment.
  • The cortisol response to ACTH stimulation remained equivalent between groups.
  • Weight gain was markedly diminished during dexamethasone treatment but normalized 10 days after cessation.
  • HPA axis function and weight gain returned to baseline levels within 10 days post-therapy.

Conclusions:

  • Seven days of high-dose dexamethasone therapy in preterm infants with BPD causes transient suppression of the HPA axis and temporary reduction in weight gain.
  • These endocrine and growth effects are reversible shortly after treatment discontinuation.

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