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Evaluation of Changes in Insulin Sensitivity in Prepubertal Small for Gestational Age Children Treated with Growth
Carmen Sydlik1, Claudia Weissenbacher1, Julia Roeb1
1Department of Pediatric Endocrinology, Dr. von Haunersches Children's Hospital, Ludwig-Maximilian-University of Munich, Lindwurmstr, Munich, Germany.
Insights
Growth hormone (GH) therapy in children born small for gestational age (SGA) can induce insulin resistance, but not to pathological levels. Monitoring glucose homeostasis is recommended, though specific risk factors remain unidentified.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Growth Hormone Therapy
Background:
- Concerns exist regarding insulin resistance and type 2 diabetes mellitus risk in children with small for gestational age (SGA) treated with growth hormone (GH).
- Current recommendations for monitoring glucose homeostasis lack consensus on methods and consequences.
Purpose of the Study:
- To analyze oral glucose tolerance tests (oGTTs) in SGA children during 4 years of GH therapy.
- To identify correlations with auxological and laboratory data.
- To find predictive baseline results for glucose homeostasis during treatment.
Main Methods:
- Yearly oral glucose tolerance tests (oGTTs) were performed in 93 prepubertal SGA children.
- Data analyzed included auxological and laboratory parameters.
- Correlation analysis and prediction of glucose homeostasis were conducted.
Main Results:
- Insulin secretion increased in the first year of GH therapy, while glucose levels remained stable.
- Insulin sensitivity index (ISI), HOMA1, HOMA2, and QUICKI stabilized after 1-2 years.
- No pathological glucose levels or diabetes mellitus cases were observed; higher gestational age, lower birth length, and older age at GH initiation were linked to lower insulin sensitivity.
- No predictive factors for later insulin resistance were identified.
Conclusions:
- GH therapy in prepubertal SGA children induces insulin resistance, but not to pathological levels.
- No specific risk factors for disturbed glucose homeostasis were identified.
- Routine oGTTs at baseline and puberty are recommended, but further surveillance strategies require re-evaluation.
Background:
Although growth hormone (GH) therapy for children born small for gestational age (SGA) has been approved for many years, there are still concerns about increasing their risk for insulin resistance and diabetes mellitus type 2. Monitoring of glucose homeostasis is therefore generally recommended, but there is no consensus on either the methods or consequences.
Methods And Aims:
The aim of our study was to analyze the oral Glucose Tolerance Tests (oGTTs) which were performed yearly from baseline to 4 years of GH therapy in a collective of 93 SGA children, who were prepubertal during the whole follow-up. We looked for correlations with auxological and laboratory data as well as predictive baseline results for glucose homeostasis during further treatment.
Results:
While glucose levels remained constant, insulin secretion increased from baseline to the first year of GH therapy. Insulin sensitivity index (ISI) showed no significant change afterwards; HOMA1, HOMA2, and QUICKI stabilized after the second year. For all indices mean values never reached pathological levels and no cases of diabetes mellitus were induced. Higher gestational age, lower birth length, and older age at start of GH therapy were associated with lower insulin sensitivity. No predictive factors for later insulin resistance could be found.
Conclusion:
As expected, in GH-treated prepubertal SGA children insulin resistance was induced, but not to pathological levels. No special risk factors for disturbed glucose homeostasis could be identified. Based on our opinion, performing oGTTs in GH-treated SGA children at baseline and in puberty should remain mandatory, but the current study recommendations regarding further surveillance of glucose homeostasis are questionable.
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