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Final height after growth hormone therapy in peripubertal boys with a subnormal integrated concentration of growth
Insights
Growth hormone (GH) therapy significantly improved final height in peripubertal boys with idiopathic short stature, reaching predicted heights. The treatment
Area of Science:
- Pediatric Endocrinology
- Growth and Development
- Hormone Therapy
Background:
- Idiopathic short stature (ISS) affects peripubertal boys, impacting final height.
- Subnormal growth hormone (GH) levels are a key indicator in ISS diagnosis.
- Assessing the efficacy of GH therapy is crucial for optimizing treatment outcomes.
Purpose of the Study:
- To evaluate the effect of recombinant human growth hormone (rhGH) therapy on final height in peripubertal boys with ISS.
- To compare the final height of treated boys with their target and predicted heights.
- To analyze growth velocity changes during rhGH treatment.
Main Methods:
- A cohort of 28 peripubertal boys with ISS and subnormal GH levels were studied.
- Eleven boys received rhGH therapy (0.75 unit/kg/week) for 2 years, followed by daily injections until final height.
- Seventeen boys served as an untreated control group, monitored until growth cessation.
Main Results:
- GH-treated boys achieved final heights closer to their target and predicted heights compared to untreated controls.
- Significant increases in height velocity were observed during the first year of GH therapy (p < 0.001).
- Untreated boys attained final heights significantly below their target and predicted heights.
Conclusions:
- Recombinant human growth hormone therapy is effective in improving final height for peripubertal boys with idiopathic short stature.
- Early intervention with GH therapy leads to accelerated growth velocity, particularly in the initial treatment year.
- The benefits of GH therapy on final height should be considered alongside treatment costs.
Abstract:
The aim of this study was to test the effect of growth hormone (GH) therapy on final height in peripubertal boys with idiopathic short stature in whom a subnormal integrated concentration of GH (< 3.2 micrograms/l) was found. Twenty-eight peripubertal children were studied. Height was below 2 SD for age, growth velocity was < 4.5 cm/year, bone age was more than 2 SD below mean for age and GH response to provocative tests was more than 10 micrograms/l. Eleven subjects (group B) were treated with recombinant GH 0.75 unit/kg/week, divided into 3 weekly doses for 2 years, and then the same weekly dose divided into daily injections was administered until final height was attained. Seventeen untreated children (group A) who were followed until cessation of growth served as controls. The GH-treated patients reached their target heights (-2.1 +/- 0.5, mean +/- SD in SDS) and predicted heights (-1.8 +/- 0.8) determined by the Bayley and Pinneau method, while the final heights of the untreated patients were significantly lower than their target heights and their predicted final heights (-2.7 +/- 0.7, -1.8 +/- 1.0 and -2.7 +/- 0.7, respectively). The main effect of GH was observed during the 1st year of treatment when height velocity was significantly higher in the GH-treated group than in the untreated one (9.3 +/- 2.1 vs. 5.3 +/- 1.1, respectively, p < 0.001). The high cost of the treatment in this specific age group should be weighed against the results.
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