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Published on: November 14, 2013
Suppression and recovery of the hypothalamic function after high-dose corticosteroid treatment in preterm infants
1Department of Pediatrics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, SAR, China. pakcheungng@cuhk.edu.hk
Insights
Systemic dexamethasone suppresses hypothalamic function in preterm infants. Partial recovery of the hypothalamic-pituitary-adrenal axis occurs four weeks after corticosteroid therapy cessation.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Pediatric Pulmonology
Background:
- High-dose systemic dexamethasone aids extubation in infants with bronchopulmonary dysplasia.
- Previous studies assessed pituitary-adrenal response but not longitudinal hypothalamic function after corticosteroid treatment in very low birth weight infants.
Purpose of the Study:
- To longitudinally monitor hypothalamic response before, during, and after a 3-week dexamethasone tapering course in very low birth weight infants.
Main Methods:
- Twenty very low birth weight infants were studied.
- Blood samples collected at weeks 0, 1, 3, and 7 for corticotropin-releasing hormone, ACTH, and cortisol levels.
- Dexamethasone treatment involved a 3-week dose-tapering course.
Main Results:
- Hormone levels were significantly suppressed during dexamethasone treatment (weeks 1 and 3).
- Pituitary function recovery began early (after week 1), while hypothalamic and adrenal recovery started post-treatment.
- At week 7, ACTH normalized, but corticotropin-releasing hormone and cortisol remained suppressed, showing partial recovery (62% and 36% of pretreatment levels, respectively).
Conclusions:
- Hypothalamic function is suppressed by systemic corticosteroids but shows partial recovery post-therapy.
- The hypothalamic-pituitary-adrenal axis in preterm infants mirrors adult responses.
- Pituitary function recovers faster than hypothalamic and adrenal functions following dexamethasone treatment.
Background:
High-dose systemic dexamethasone is effective in facilitating extubation of ventilated infants with bronchopulmonary dysplasia. Although the suppression and recovery of pituitary-adrenal response had been assessed after corticosteroid treatment in very low birth weight infants, its effect on hypothalamic function has not been longitudinally monitored.
Aims:
This study was designed to assess the longitudinal hypothalamic response before, during and 4 weeks after a 3-week dose-tapering course of systemic dexamethasone treatment.
Patients And Methods:
Twenty very low birth weight infants had blood collected for corticotropin-releasing hormone, ACTH and cortisol measurements immediately before starting dexamethasone (week 0), after receiving the maximum dose of treatment (week 1), at the end of the 3-week course (week 3) and 4 weeks after stopping corticosteroids (week 7).
Results:
All circulating hormone concentrations were significantly suppressed during the treatment period at week 1 and week 3 compared with pretreatment concentrations at week 0 (p < 0.001). The recovery of pituitary function started early soon after week 1, whereas that of hypothalamus and adrenal functions started after the end of the dexamethasone course. Plasma ACTH concentration at week 7 had returned to the pretreatment level, but plasma corticotropin-releasing hormone (p < 0.05) and serum cortisol (p < 0.001) concentrations remained significantly suppressed. Partial recovery of hypothalamic and adrenal function was observed at week 7 (62 vs. 36% of their pretreatment levels, respectively).
Conclusion:
Our findings suggest that the hypothalamic function is suppressed during systemic corticosteroid treatment but partial recovery occurs 4 weeks after stopping therapy. Even in preterm infants, the hypothalamic-pituitary-adrenal axis behaves in a similar manner as in adult subjects and the pituitary function recovers earlier than that of hypothalamus and adrenals.
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