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Updated: Aug 13, 2026

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Published on: June 29, 2013
[Insulin receptors in intrauterine growth retardation]
J Jordán1, M C Blasco, M G Juste
1Departamento de Pediatría y Puericultura, Facultad de Medicina, Hospital Clínico Universitario de Zaragoza.
Insights
Neonatal small for gestational age infants show increased insulin sensitivity due to altered erythrocyte insulin receptors. This suggests a compensatory mechanism in response to chronic undernutrition.
Area of Science:
- Endocrinology
- Neonatal Physiology
- Metabolic Research
Context:
- Neonatal period is critical for metabolic development.
- Intrauterine growth restriction (IUGR) impacts infant physiology.
- Erythrocyte insulin receptors play a role in glucose homeostasis.
Purpose:
- To analyze erythrocyte insulin binding and receptors in newborns.
- To compare insulin sensitivity in term infants versus small for gestational age (SGA) infants.
- To investigate the relationship between birth weight and insulin receptor characteristics in SGA infants.
Summary:
- Studied 30 normal and 15 SGA newborns, measuring cord blood insulin binding, receptors, glucose, insulin, C-peptide, and C-peptide/insulin ratio.
- SGA infants exhibited significantly lower affinity and higher dissociation constants for erythrocyte insulin receptors (p=0.05).
- A negative correlation was found between the number of insulin receptor sites per cell and birth weight in SGA infants (r=-0.57, p<0.05).
Impact:
- Findings suggest increased insulin sensitivity in SGA infants, potentially due to receptor upregulation as a response to chronic undernutrition.
- Provides insights into the mechanisms of insulin resistance and adaptation in growth-restricted neonates.
- Highlights the importance of erythrocyte insulin receptor analysis for understanding neonatal metabolic adaptation.
Abstract:
This report analyses erythrocyte insulin binding and specific erythrocyte insulin receptors in the neonatal period. Authors have studied thirty normal newborns who had an adequate weight for their gestational age and another fifteen who were asymmetric intrauterine retarded growth. Cord blood samples were collected and insulin binding, insulin receptors, blood glucose concentration, serum immunoreactive insulin, serum C-peptide concentration and molar ratio of C-peptide to insulin were determined. Insulin and C-peptide sera concentrations suggest that basal insulin secretion in small for data newborns is similar to term infants. Significantly minor affinity constant (p = 0.05) and significantly major dissociation constant (p = 0.05) in small for date infants versus newborns adequately weighted for their gestational age, justify the increased sensitivity to insulin as it happens in other states of chronic undernutrition. In small for date infants, number of sites per cell correlates negatively (r = -0.57, p less than 0.05) with birth weight. Up regulation mechanism that modulates receptors concentration could explain this phenomenon.
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