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Growth hormone therapy in children with partial growth hormone deficiency. Are we treating the right patients?
Barbara Krukowska-Andrzejczyk1, Maria Kalina2, Barbara Kalina-Faska2
1Division of Pediatrics and Neurology of Developmental Age, The Independent Public Clinical Hospital No. 6 of the Medical University of Silesia in Katowice, John Paul II Upper Silesian Child Health Centre, Poland.
Insights
Recombinant human growth hormone (rhGH) therapy did not show significant benefits for children with partial growth hormone deficiency (pGHD) compared to untreated idiopathic short stature (ISS). Further research is needed to establish better criteria for initiating rhGH treatment in these children.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Short Stature
Background:
- Diagnosis of growth hormone deficiency (GHD) in children relies on GH stimulation tests, but cut-off values are inconsistent.
- Indications for recombinant GH (rhGH) therapy are debated, especially for partial GHD (pGHD) with GH levels between 5-10 ng/ml.
Purpose of the Study:
- To evaluate the effects of rhGH therapy in children with transient pGHD.
- To compare rhGH-treated pGHD children with a control group of untreated idiopathic short stature (ISS) children.
Main Methods:
- A study group of 54 children with pGHD received rhGH treatment.
- A control group of 32 children with ISS, matched for age and sex, did not receive rhGH treatment.
Main Results:
- Both groups achieved final heights within normal population ranges.
- While both groups showed height gain, the difference was not statistically significant after excluding children with familial short stature (FSS).
Conclusions:
- rhGH treatment did not demonstrate clear benefits for children with pGHD compared to untreated ISS.
- New criteria beyond arbitrary GH concentration levels are necessary for guiding rhGH treatment decisions in pGHD.
Introduction:
Diagnosis of growth hormone deficiency (GHD) in children with short stature, whose height is below -2SD for the population norm, is based on the assessment of growth hormone (GH) peaks in stimulation tests. However, cut-off values for GH secretion are arbitrary and vary in different centres. Indications for recombinant GH therapy remain disputable in children with GH concentrations between 5 and 10 ng/ml (pGHD).
Aim Of The Study:
The aim of our study was to assess the effects of rhGH therapy in children with transient pGHD deficiency compared to untreated children with idiopathic short stature (ISS).
Material And Methods:
The study group comprised 54 patients at the mean age of 13.5 (SD 2.36) years, who were diagnosed as pGHD and treated with rhGH. The control group comprised 32 subjects with ISS matched for sex and age, untreated with rhGH.
Results:
Mean final height was within the normal range for population norms in both groups. The average height gain was statistically significant at -1.3 SD (p < 0.001) for the study group and -1.02 SD (p ≤ 0.001) for the control group. However after exclusion of children with familial short stature (FSS) the height gains were, respectively, 1.41 SD ±0.67 for the study group and 1.22 SD ±0.77 for the control group, without statistical significance.
Conclusions:
The results of our study did not show beneficial effects of rhGH treatment in children with pGHD as compared to untreated ISS subjects. Therefore, it is necessary to determine criteria other than arbitrarily established GH concentration for starting rhGH treatment in children with pGHD.
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