Relationship between insulin sensitivity and IGF-I sensitivity in low birth weight prepubertal children
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Updated: Mar 18, 2026

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Rossana Román1, German Iñiguez, Teresa Salazar
1Institute of Maternal and Child Research, University of Chile, Santiago, Chile.
Insights
Low birth weight children with lower insulin sensitivity also show reduced insulin-like growth factor-I (IGF-I) sensitivity. This suggests impaired responses to both insulin and IGF-I may coexist in some low birth weight individuals.
Area of Science:
- Pediatric endocrinology
- Metabolic disorders
- Growth factors
Background:
- Insulin-like growth factor-I (IGF-I) and insulin share similar biological pathways.
- Reduced sensitivity to these hormones may impact growth and metabolism.
Purpose of the Study:
- To investigate potential coexisting decreased sensitivity to insulin and IGF-I in low birth weight (LBW) children.
- To explore the relationship between insulin sensitivity and IGF-I sensitivity in this population.
Main Methods:
- Studied 48 prepubertal LBW children (mean age 7.6 years).
- Assessed insulin sensitivity via oral glucose tolerance test (OGTT).
- Evaluated IGF-I sensitivity by measuring nocturnal growth hormone (GH) response to recombinant human IGF-I/IGFBP-3 complex.
Main Results:
- LBW children were stratified into quartiles based on insulin sensitivity.
- Those in the lowest quartile of insulin sensitivity demonstrated significantly lower IGF-I sensitivity.
- A greater reduction in GH AUC was observed in the least insulin-sensitive group compared to the most sensitive group.
Conclusions:
- Reduced insulin sensitivity in LBW children is associated with diminished IGF-I sensitivity.
- These findings suggest that impaired insulin and IGF-I signaling may occur concurrently in some prepubertal LBW children.
- This highlights potential metabolic and growth challenges in this cohort.
Background:
Insulin-like growth factor-I (IGF-I) and insulin are structurally related proteins with similar receptors and signal transduction systems.
Aim:
We postulate that some low birth weight (LBW) children may have decreased sensitivity to both insulin and IGF-I.
Methods:
We studied 48 prepubertal LBW children aged 7.6 +/- 2.4 years. Insulin sensitivity was determined using an oral glucose tolerance test, and IGF-I sensitivity was assessed by determining nocturnal GH concentrations at baseline and after administration of recombinant human IGF-I/IGFBP-3 complex.
Results:
Children were classified into quartiles of insulin sensitivity based on their glucose AUC/insulin AUC index. Children in the lowest quartile of insulin sensitivity exhibited a lower IGF-I sensitivity after administration of the rhIGF-I/rhIGFBP-3 complex compared to children in the highest quartile of insulin sensitivity (percent change in GH AUC: -44.2 +/- 5.7 vs. -21.6 +/- 6.8, p < 0.05).
Conclusion:
LBW children in the lowest quartile of insulin sensitivity exhibited a lower pituitary GH response to the administration of rhIGF-I/rhIGFBP-3. Our findings suggest that reduced sensitivity to insulin and IGF-I may coexist in some prepubertal LBW children.
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