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Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Metabolic impact of growth hormone treatment in short children born small for gestational age
Jan Lebl1, Yael Lebenthal, Stanislava Kolouskova
1Department of Pediatrics, Second Faculty of Medicine, Charles University, Prague, Czech Republic.
Insights
Growth hormone (GH) therapy in short small for gestational age (SGA) children reduced ghrelin and leptin. This suggests GH may improve long-term metabolic health by influencing appetite and body composition.
Area of Science:
- Pediatric Endocrinology
- Metabolic Research
- Growth Hormone Therapy
Background:
- Short children born small for gestational age (SGA) may experience metabolic changes with growth hormone (GH) treatment.
- Potential long-term metabolic effects require investigation.
Purpose of the Study:
- To evaluate the metabolic effects of different doses and durations of GH therapy in short SGA children.
- To assess changes in key metabolic hormones and markers.
Main Methods:
- 149 short SGA children were randomized to low, mid, or high-dose GH therapy for 1 or 2 years.
- Leptin, ghrelin, IGF-I, IGFBP-1, lipids, glucose, and insulin were measured at baseline and 12/24 months.
Main Results:
- GH treatment significantly reduced ghrelin and leptin levels after 1 year.
- Insulin levels increased, while IGF-I SDS and IGFBP-1 decreased.
- Ghrelin showed an inverse correlation with IGF-I SDS.
Conclusions:
- GH treatment in short SGA children may reduce ghrelin and leptin via the GH-IGF-I axis.
- This hormonal modulation could impact food intake and body composition.
- GH therapy holds potential for improving long-term metabolic outcomes in this population.
Background:
Growth hormone (GH) treatment in short children born small for gestational age (SGA) may result in metabolic changes with potential long-term effects.
Methods:
149 short SGA children (mean birth weight 2.0 ± 0.6 kg, age 5.5 ± 1.5 years, height standard deviation score (SDS) -3.1 ± 0.6) were randomised to: low-dose GH therapy (0.033 mg/kg/day) for 2 years; high-dose GH therapy (0.100 mg/kg/day) for 1 year, or mid-dose GH therapy (0.067 mg/kg/day) for 1 year. Leptin, ghrelin, insulin-like growth factor-I (IGF-I), IGF binding protein-1 (IGFBP-1), lipids, fasting blood glucose and fasting insulin were assessed at baseline, 12 and 24 months.
Results:
After 1 year of active treatment, GH significantly reduced serum ghrelin and increased IGF-I SDS and insulin levels. Regression analysis showed an inverse correlation between ghrelin and IGF-I SDS (p < 0.001). Leptin and IGFBP-1 also declined (both p < 0.05). Changes in insulin levels reversed upon discontinuation. Improvements in lipid profile were nonsignificant and fasting blood glucose levels remained within the normal range.
Conclusion:
In short SGA children, ghrelin and leptin reductions associated with GH treatment may occur through a negative feedback loop of the GH-IGF-I axis. Consequently, via ghrelin and leptin suppression, GH treatment may modify food intake and body composition and potentially improve long-term metabolic outcomes.
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