Effect of corticoid therapy on growth hormone secretion
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Published on: January 25, 2016
M Bozzola1, F Locatelli, D Gambarana
1Pediatric Clinic, University of Pavia, IRCCS Policlinico San Matteo, Italy.
Insights
Corticosteroid treatment in children with leukemia suppresses growth hormone (GH) release. GH secretion partially recovers after stopping steroids, but insulin-like growth factor 1 levels remain low, indicating potential long-term growth impairment.
Area of Science:
- Pediatric Endocrinology
- Pediatric Oncology
Background:
- Exogenous corticosteroids are known to inhibit linear growth in children.
- Children with acute lymphoblastic leukemia often receive corticosteroid therapy as part of their treatment.
Purpose of the Study:
- To investigate the mechanisms of growth failure during corticosteroid treatment in children with acute lymphoblastic leukemia.
- To evaluate the impact of high-dose prednisone on growth hormone (GH) secretion and recovery after drug withdrawal.
Main Methods:
- Short-term high-dose prednisone treatment was administered to 7 prepubertal children with acute lymphoblastic leukemia.
- Growth hormone (GH) release was assessed during sleep and in response to arginine, insulin, and GH-releasing hormone (GHRH) before, during, and after steroid treatment.
- Insulin-like growth factor 1 (IGF-1) levels were also measured.
Main Results:
- Corticosteroid therapy significantly suppressed GH secretion during sleep and in response to stimuli.
- GH responsiveness partially recovered after steroid discontinuation, particularly to GHRH and arginine.
- Insulin-like growth factor 1 (IGF-1) levels remained low even after steroid withdrawal, suggesting persistent growth impairment.
Conclusions:
- High-dose corticosteroid treatment impairs GH secretion in children with acute lymphoblastic leukemia.
- While GH secretion shows partial recovery after steroid withdrawal, sustained low IGF-1 levels indicate potential for long-term growth failure.
- The adrenergic response to insulin may not immediately recover following corticosteroid discontinuation.
Abstract:
Exogenous corticoids are known to be potent inhibitors of linear growth in children. We investigated the mechanisms underlying growth failure by evaluating growth hormone (GH) release during short-term high-dose prednisone treatment (40 mg/m2/day given orally in 3 divided doses) and 7 days after steroid withdrawal in 7 prepubertal children (4 males, 3 females, age range 3-12 years), affected by acute lymphoblastic leukemia. Patients also received weekly administrations of vincristine (1.5 mg/m2 i.v.), daunomycin (20 mg/m2 i.v.) and L-asparaginase (6,000 IU/m2 i.m.). Corticoid therapy suppressed GH secretion during deep sleep as well as in response to arginine, insulin and GH-releasing hormone (GHRH) administration. A significant recovery of GH responsiveness after drug discontinuation was observed during deep sleep (14.03 +/- 3.47 vs. 1.49 +/- 0.43 ng/ml, p less than 0.025) as well as in response to arginine (13.63 +/- 2.73 vs. 4.95 +/- 1.54 ng/ml, p less than 0.025) and GHRH (32.62 +/- 4.59 vs. 7.27 +/- 3.52 ng/ml, p less than 0.005) but not to insulin (7.12 +/- 0.88 vs. 4.47 +/- 0.96 ng/ml, p = NS). Insulin-like growth factor 1 levels during deep sleep (0.61 +/- 0.13 IU/ml/min) were found to be low in the course of steroid therapy and did not increase after drug withdrawal (0.41 +/- 0.07 IU/ml/min). Our preliminary data suggest that recovery of adrenergic response to insulin does not immediately follow corticosteroid discontinuation.
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