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Updated: Aug 10, 2026

Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Insulin sensitivity in growth hormone-deficient children: influence of replacement treatment
Giorgio Radetti1, Bruno Pasquino, Elena Gottardi
1Department of Paediatrics, Regional Hospital of Bolzano, Italy. giorgio.radetti@asbz.it
Insights
Growth hormone (GH) treatment in children with GH deficiency does not cause diabetes. However, it significantly reduces insulin sensitivity (IS) during the first year of therapy.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Growth Hormone Therapy
Background:
- Excessive growth hormone (GH) secretion in adults can cause secondary diabetes mellitus.
- Prolonged GH treatment may increase the risk of type 2 diabetes mellitus in susceptible children.
Purpose of the Study:
- To evaluate insulin sensitivity (IS) and glucose tolerance (GT) in GH-deficient children undergoing 6 years of GH treatment.
- To assess the long-term impact of GH therapy on metabolic health in pediatric patients.
Main Methods:
- Study included 128 children (88 males, 40 females) with GH deficiency.
- GH administered subcutaneously at 0.3 mg/kg weekly for 6 years.
- Insulin sensitivity assessed using the quantitative insulin sensitivity check index (QUICKI); glucose tolerance evaluated using established diabetes classification criteria.
Main Results:
- No instances of impaired glucose tolerance or diabetes were observed during the 6-year follow-up.
- Insulin sensitivity, initially lower than controls, significantly decreased in the first year of GH therapy (QUICKI: 0.346 ± 0.033 vs. 0.355 ± 0.044, P < 0.05).
- No further decline in IS was noted in subsequent years; no correlation found between QUICKI, BMI, treatment duration, and puberty onset.
Conclusions:
- GH treatment in GH-deficient children is safe regarding glucose tolerance and does not induce type 2 diabetes mellitus.
- GH therapy significantly diminishes insulin sensitivity in these children, particularly within the first year of treatment.
Objective:
In adults, excessive GH secretion may lead to secondary diabetes mellitus, while prolonged GH treatment may accelerate the onset of type 2 diabetes mellitus in predisposed children. The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group of GH-deficient children treated with GH for a period of 6 years.
Patients And Design:
One hundred and twenty-eight children (40 females, 88 males) were included in the study. At the beginning of treatment chronological age was 8.9 +/- 3.2 years, height standard deviation score (SDS) -2.43 +/- 0.90 and body mass index (BMI) SDS 0.18 +/- 1.60. At the end of the study chronological age was 13.0 +/- 2.9 years, height SDS -1.24 +/- 1.27 and BMI SDS 0.23 +/- 1.54. GH was administered at a mean weekly dosage of 0.3 mg/kg, injected subcutaneously over 6-7 days. GT was assessed according to the criteria of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. IS was evaluated with the quantitative insulin sensitivity check index (QUICKI).
Results:
No cases of impaired GT or diabetes were recorded during the follow-up period. IS, already lower than in controls before starting treatment with GH, decreased significantly during the first year of therapy (QUICKI: 0.346 +/- 0.033 vs. 0.355 +/- 0.044, P < 0.05), with no further decrease in the following years. No correlation was found between QUICKI, BMI, years of treatment and onset of puberty.
Conclusions:
GH treatment in GH-deficient children does not lead to an impaired GT or type 2 diabetes mellitus, although it does significantly decrease IS.
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