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Published on: January 20, 2015
Metabolic effects of human growth hormone in corticosteroid-treated children
Insights
Corticosteroids impair human growth hormone (HGH) effectiveness in dwarfed children, causing resistance to HGH treatment. This antagonism at the tissue level explains growth retardation in steroid-treated children.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Pharmacology
Background:
- Children with chronic diseases often require long-term corticosteroid therapy.
- Corticosteroids can impact various physiological processes, including growth.
- Human growth hormone (HGH) is used to treat growth disorders in children.
Purpose of the Study:
- To evaluate the effects of administered human growth hormone (HGH) in dwarfed, prepubertal children receiving long-term corticosteroid therapy.
- To determine if corticosteroids antagonize the effects of HGH on growth and metabolism.
Main Methods:
- Conducted 11 metabolic balance studies in prepubertal children.
- Administered HGH to corticosteroid-treated children, hypopituitary subjects, and asthmatic children not on corticosteroids.
- Monitored nitrogen, phosphorus, and potassium retention and growth rates.
Main Results:
- Corticosteroid-treated children showed impaired HGH response with minimal nitrogen and no phosphorus retention.
- Hypopituitary and non-corticosteroid-treated asthmatic children responded to HGH with significant retention.
- Corticosteroid-treated children receiving high-dose HGH showed no growth improvement, unlike hypopituitary subjects.
Conclusions:
- Dwarfism in children on corticosteroid therapy is likely due to corticosteroid-induced antagonism of HGH effects at the peripheral tissue level.
- Corticosteroids significantly inhibit the metabolic and growth-promoting actions of HGH.
- This finding has implications for managing growth in children requiring long-term corticosteroid treatment.
Abstract:
The effects of administered human growth hormone (HGH) were evaluated in dwarfed, prepubertal children who were receiving long-term corticosteroid therapy for a chronic disease. During 11 complete metabolic balance studies, the eight corticosteroid-treated children demonstrated impaired response to large doses of HGH with minimal nitrogen and no phosphorus retention. In contrast, two hypopituitary subjects and two asthmatic children not receiving corticosteroid responded to the same preparations of HGH with nitrogen, potassium, and phosphorus retention. Six corticosteroid-treated children were given large doses of HGH (40-120 mg/wk for 4 to 8 months and showed no improvement in their retarded rate of growth, whereas the hypopituitary subjects showed accelerated growth during administration of 10-15 mg of HGH/wk. It is concluded that dwarfism in steroid-treated children results from corticosteroid-induced antagonism of the effects of HGH at the peripheral tissue level.
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