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Published on: October 17, 2013
Treatment of children and adolescents with idiopathic short stature
1University Children's Hospital Tübingen, Hoppe-Seyler-Strasse 1, D-72076 Tübingen, Germany. michael.ranke@gmx.de
Insights
Idiopathic short stature (ISS) treatment options include counseling and medical interventions. Growth hormone therapy is approved for children with ISS, though optimal dosing and long-term safety require further research.
Area of Science:
- Pediatrics
- Endocrinology
- Genetics
Background:
- Idiopathic short stature (ISS) is characterized by childhood shortness without a clear underlying cause.
- ISS can be familial or nonfamilial and may present with or without delayed puberty.
- Psychological burden associated with short stature necessitates treatment considerations.
Purpose of the Study:
- To review current and experimental treatment modalities for idiopathic short stature.
- To discuss the efficacy and limitations of various therapeutic approaches, including growth hormone therapy.
- To address the ongoing debate regarding the psychological benefits versus medicalization of height increase.
Main Methods:
- Review of existing literature on idiopathic short stature treatments.
- Analysis of hormonal therapies, including sex steroids, GnRH agonists, aromatase inhibitors, and growth hormone.
- Examination of evidence regarding effects on height velocity, growth tempo, and adult height.
Main Results:
- Sex steroids can improve height velocity but do not affect adult height.
- Experimental medications like GnRH agonists and aromatase inhibitors may increase adult height.
- Growth hormone therapy is approved for ISS and can increase height, but requires higher doses than replacement and needs optimization for efficacy, cost, and safety.
Conclusions:
- Growth hormone therapy is an established treatment for ISS, though optimization is needed.
- Experimental therapies show potential but require further investigation.
- A critical discussion on the psychological benefits and potential medicalization of height is ongoing.
Abstract:
Idiopathic short stature (ISS) is defined as shortness in childhood without a specific cause. ISS may be familial or nonfamilial and may be associated with or without delay of pubertal development. Treatment can be considered in an attempt to reduce the psychological burden caused by short stature in childhood and adult life. If counselling alone is not sufficient, medical modifications of the growth process can be attempted. In cases with pubertal delay, sex steroids, such as testosterone and oxandrolone, can favourably influence height velocity and growth tempo, although adult height is not affected. Medications that prolong the process of growth--for example, gonadotropin-releasing hormone agonists or aromatase inhibitors--might increase adult height, but findings to date are still experimental. Growth hormone therapy is approved for the treatment of very short children with reduced adult height expectation, as evidence has accumulated that this therapy can increase height in childhood and in adult life. Sensitivity to growth hormone is impaired in patients with ISS; therefore, doses higher than a replacement dose have to be applied. This treatment still needs to be optimized in terms of efficacy, cost-effectiveness and long-term safety. A debate is ongoing concerning the psychological benefit of height increase, with clinicians warning against the medicalization of a deviation in height.
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