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Growth hormone increases final height in patients with juvenile idiopathic arthritis: data from a randomized
Susanne Bechtold1, Peter Ripperger, Robert Dalla Pozza
1University Children's Hospital, Division of Endocrinology and Diabetology, Munich, Germany. Susanne.Bechtold@med.uni-muenchen.de
Insights
Growth hormone (GH) therapy significantly improves final height in children with juvenile idiopathic arthritis (JIA). This long-term treatment offers a beneficial effect on growth for most affected children.
Area of Science:
- Pediatric Endocrinology
- Rheumatology
- Growth Hormone Therapy
Background:
- Growth hormone (GH) is known to stimulate growth in children with juvenile idiopathic arthritis (JIA).
- However, the long-term impact of GH therapy on achieving final adult height in these patients remains unclear.
Purpose of the Study:
- To investigate the long-term efficacy of growth hormone (GH) therapy on final height in growth-retarded children diagnosed with severe forms of juvenile idiopathic arthritis (JIA).
- To assess the influence of disease activity on treatment outcomes and identify potential adverse events.
Main Methods:
- A controlled study involving 31 growth-retarded children with systemic and polyarticular JIA.
- 13 patients received GH treatment (0.33 mg/kg/week) for a mean of 6.7 years, while 18 served as an untreated control group.
- Final height was assessed after a mean observational period of 8.4 years.
Main Results:
- GH-treated patients achieved a mean height increase of 1.6 SD, while the control group experienced a height loss of -0.7 SD.
- Mean final height was significantly greater in the GH group (-1.6 SD) compared to the control group (-3.4 SD).
- More GH-treated patients reached their target height (11/13 vs. 4/18). Moderate disease activity correlated with the best outcomes. No adverse events were reported.
Conclusions:
- Long-term growth hormone (GH) therapy demonstrates a beneficial effect on final height for the majority of growth-retarded children with severe juvenile idiopathic arthritis (JIA).
- The positive impact on growth is significant even after adjusting for disease activity, with patients experiencing moderate disease activity showing the most benefit.
Background:
GH treatment stimulates growth in short children with juvenile idiopathic arthritis (JIA). The extent to which this therapy increases final height is not known.
Methods:
Thirty-one growth-retarded children with systemic and polyarticular idiopathic arthritis were enrolled in this controlled study. After a mean observational time of 8.4 yr, final height was reached in 13 patients (seven females and six males) treated with GH for a mean of 6.7 yr in a dose of 0.33 mg/kg body weight per week. Eighteen patients (12 females and six males) served as an untreated control group.
Results:
Mean increment in height in the treatment group was 1.6 +/- 0.8 SD, whereas the patients of the control group lost 0.7 +/- 1.8 SD. Overall, mean final height in the treatment group was -1.6 SD and in the control group -3.4 SD. More GH-treated patients reached a final height within target height than untreated patients (11 of 13 vs. four of 18). Disease activity markers had a significant influence on height outcome. After adjustment for baseline and average disease activity, the difference between treatment and control group was still significant (mean 1.5 SD). Patients with a moderate overall disease activity profited most from GH treatment. No adverse events were noted throughout the study.
Conclusion:
Our data suggest that long-term GH therapy has a beneficial effect on growth and final height in the majority of growth retarded children with severe forms of JIA.
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