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Published on: January 7, 2016
Serum leptin in short children born small for gestational age: dose-dependent effect of growth hormone treatment
M C Boguszewski1, F de Zegher, K Albertsson-Wikland
1International Pediatric Growth Research Center, Department of Pediatrics, University of Göteborg, Göteborg, Sweden. margabogus@bol.com.br
Insights
Growth hormone (GH) treatment transiently reduces serum leptin levels in short children born small for gestational age (SGA) in a dose-dependent manner. Leptin levels returned to baseline after GH treatment withdrawal.
Area of Science:
- Pediatric Endocrinology
- Metabolic Research
- Growth Hormone Therapy
Background:
- Children born small for gestational age (SGA) often experience growth issues.
- Leptin, a hormone regulating appetite and metabolism, plays a role in growth.
- Understanding leptin dynamics during growth hormone (GH) treatment is crucial for SGA children.
Purpose of the Study:
- To investigate the impact of varying growth hormone (GH) regimens on serum leptin levels.
- To assess leptin level changes in short prepubertal children born small for gestational age (SGA).
Main Methods:
- Multicenter trials involving 78 short prepubertal SGA children.
- Randomization to untreated or GH treatment groups (0.1, 0.2, or 0.3 IU/kg/day) for 2 years.
- Follow-up treatment and discontinuation phases were implemented.
Main Results:
- A significant, dose-dependent decrease in serum leptin was observed during the first year of GH therapy.
- Leptin levels decreased by 13%, 23%, and 32% with increasing GH doses (0.1, 0.2, 0.3 IU/kg).
- Upon cessation of high-dose GH treatment, serum leptin levels reverted to pretreatment levels within one year.
Conclusions:
- Growth hormone (GH) treatment induces a transient, dose-dependent reduction in serum leptin in short SGA children.
- The most significant alterations in serum leptin occurred within the first year of initiating and withdrawing GH therapy.
Objective:
To study the effects of different regimens of growth hormone (GH) treatment on serum leptin levels in 78 short prepubertal children born small for gestational age (SGA).
Methods:
The children were originally included in two independent multicenter trials, one in Belgium and one in the Nordic countries. SGA children were randomized either to remain untreated or to be treated with GH at a daily dose of 0.1, 0.2 or 0.3 IU/kg for 2 years. Thereafter, treatment was continued for another 2 years in the Nordic children, whereas it was discontinued in the Belgian children.
Results:
In the GH treatment groups, a significant dose-dependent decrease in leptin levels was found during the first year of therapy, with a mean decrease of 13, 23 and 32% in the groups receiving GH at 0.1, 0.2 and 0.3 IU/kg, respectively. When high-dose treatment was interrupted, serum leptin increased within 1 year to pretreatment levels.
Conclusion:
Serum leptin levels in short children born SGA are transiently reduced by GH treatment in a dose-dependent fashion. The most pronounced changes in serum leptin were documented within the first year after initiation and withdrawal of high-dose GH treatment.
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