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Updated: Aug 17, 2026

Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Metabolic effects of growth hormone in the child and adolescent
1University of South Florida College of Medicine, Tampa, Florida, USA. shulmand@allkids.org
Insights
Growth hormone therapy shows metabolic benefits in children, improving bone density and body composition. Close monitoring for potential diabetes risk is recommended, alongside reassurances regarding tumor recurrence and transplant outcomes.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Growth Hormone Therapy
Background:
- Growth hormone (GH) therapy is used for various pediatric conditions.
- Understanding its metabolic effects and safety profile is crucial for clinical practice.
- Previous studies have indicated potential benefits and risks associated with GH treatment.
Purpose of the Study:
- To review and synthesize original studies published in 2000 on the metabolic effects of GH therapy in pediatric patients.
- To assess the impact of GH on glucose metabolism, bone health, body composition, skin properties, and safety outcomes (tumors, transplantation).
Main Methods:
- Systematic review and synthesis of original research studies published in the year 2000.
- Analysis of data from the Pharmacia International Growth Study database.
- Inclusion of studies focusing on pediatric patients with conditions like intrauterine growth retardation, Turner syndrome, chronic renal failure, Prader-Willi syndrome, and brain tumors.
Main Results:
- GH therapy rarely caused glucose tolerance abnormalities but increased insulin levels in some groups.
- GH increased bone turnover markers and bone mineral density in children with chronic renal failure and Prader-Willi syndrome.
- GH reduced body fat, improved physical skills, and increased lean mass in Prader-Willi syndrome; leptin levels decreased dose-dependently in intrauterine growth retardation.
- GH improved skin thickness and reduced stiffness in GH-deficient children.
- No increased risk of tumor recurrence or mortality was observed in brain tumor patients.
- GH did not adversely affect graft survival or rejection episodes in children awaiting kidney transplantation.
Conclusions:
- Growth hormone therapy offers significant metabolic and physical benefits in various pediatric conditions.
- Continued surveillance for type 2 diabetes is warranted in GH-treated patients.
- GH therapy appears safe concerning tumor recurrence and kidney transplant outcomes in pediatric populations.
Abstract:
During the year 2000, several original studies were published regarding the metabolic effects of growth hormone therapy in pediatric patients. Pharmacologic doses of growth hormone were rarely associated with abnormalities in glucose tolerance in children with intrauterine growth retardation and Turner syndrome; however, serum insulin levels were elevated. A report from the Pharmacia International Growth Study database suggested a possible increase in type 2 diabetes in growth hormone-treated patients, indicating the need for continued surveillance for this condition. Growth hormone therapy increased markers of bone turnover and bone mineral density in children with chronic renal failure and Prader-Willi syndrome. In Prader-Willi syndrome, 2 years of growth hormone therapy also induced a sustained decrease in body fat, improvement in strength and physical skills, and increased lean body mass. Serum leptin, a reflection of body fat, declined with growth hormone therapy in a dose-dependent manner in intrauterine growth retardation children; the magnitude of the decline correlated with linear growth response. Skin is a target organ for growth hormone in children; growth hormone increased dermal thickness and reduced skin stiffness in growth hormone-deficient children. Reassuring data were published regarding the risk of tumor recurrence and mortality in children with brain tumors treated with growth hormone. Growth hormone administered to short children prior to kidney transplantation did not have adverse effects on subsequent graft survival or number of rejection episodes.
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