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Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Growth hormone-releasing hormone reverses secondary somatotroph unresponsiveness
T E Romer1, B Rymkiewicz-Kluczynska, M Olivier
1Child Health Center, Warsaw, Poland.
Insights
Growth hormone-releasing hormone (GHRH) treatment in children with severe growth hormone deficiency (GHD) improved pituitary responsiveness over six months. Some patients showed enhanced growth, suggesting GHRH therapy may benefit specific GHD cases.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Hormone Replacement
Background:
- Severe growth hormone deficiency (GHD) in prepubertal children presents significant growth challenges.
- Assessing pituitary responsiveness to growth hormone-releasing hormone (GHRH) is crucial for treatment efficacy.
Purpose of the Study:
- To evaluate the effect of GHRH 1-44 treatment on pituitary GH secretion and growth velocity in severely GHD children.
- To explore the relationship between GHRH stimulation, growth response, and patient characteristics.
Main Methods:
- Twenty prepubertal children with severe GHD received subcutaneous GHRH 1-44 (10 mcg/kg) for six months, either daily or thrice weekly.
- Acute intravenous GHRH tests were conducted before, and at 2 and 6 months of treatment to measure peak GH responses.
- Growth velocity (GV) was monitored throughout the treatment period.
Main Results:
- Mean peak GH responses to acute GHRH tests significantly increased from baseline (2.92 mcg/L) to 6 months (7.56 mcg/L) (P < 0.05).
- Mean growth velocity during treatment was 2.99 cm/yr, with only two patients showing >2 cm/yr increase.
- A positive correlation was observed between GV and pre-treatment peak GH response (r=0.68, P < 0.005), and a negative correlation between GH response and bone age (r=-0.46, P < 0.05).
Conclusions:
- Six months of GHRH treatment can enhance pituitary responsiveness in some severely GHD children, even those initially unresponsive.
- The duration and severity of GHD may influence the somatotrophs' ability to respond to GHRH stimulation.
- GHRH therapy shows potential for improving pituitary function in select GHD pediatric populations.
Abstract:
Twenty severely GH-deficient prepubertal children aged 10.7 +/- 2.1 yr (mean +/- SD) and with a height SD of -4.92 +/- 1.02 were treated with sc injections of GHRH 1-44 (10 micrograms/kg BW) for 6 months either daily (11 patients) or 3 times/week (nine patients). An acute iv GHRH test (2 micrograms/kg BW) was performed before and after 2 and 6 months of treatment. Mean (+/- SD) peak GH responses to these tests were 2.92 +/- 3.01, 4.57 +/- 4.91, and 7.56 +/- 8.14 micrograms/L, respectively (P less than 0.05, pretreatment vs. 6 months). The mean growth velocity (GV) during treatment was only 2.99 +/- 1.67 cm/yr and only two patients increased their GV by more than 2 cm/yr. A correlation was found between GV during treatment and the peak serum GH response to GHRH acute test before treatment (r = 0.68, P less than 0.005) as well as between GH response to the acute test and patient's bone age (r = -0.46, P less than 0.05). The results indicate that in some severely GHD patients with no response to GHRH even after a 2-month priming period, 6 months of treatment with GHRH can evoke pituitary responsiveness. We speculate that the duration of the GHRH deficiency and its severity plays a role in the ability of somatotrophs to respond to this stimulus.
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