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Effects of oral glucose and protein load on plasma glucagon and insulin concentrations in small for gestational age

Pediatric Research
|February 1, 1977
PubMed

Insights

Small for gestational age (SGA) and appropriate for gestational age (AGA) newborns show similar pancreatic hormone secretion in early life. This study compared glucose, insulin, and glucagon levels in both groups after a nutrient load.

Area of Science:

  • Neonatal endocrinology
  • Pediatric metabolism
  • Perinatal physiology

Background:

  • Infants small for gestational age (SGA) may exhibit altered metabolic responses.
  • Understanding glucose, insulin, and glucagon dynamics is crucial for neonatal care.
  • Limited data exists on the hormonal responses of SGA infants to nutrient loads in the first 48 hours of life.

Purpose of the Study:

  • To compare portal and peripheral blood glucose, insulin, and glucagon levels in SGA and appropriate for gestational age (AGA) newborns.
  • To investigate the hormonal responses of these infants to an oral glucose and protein load within the first 48 hours of life.

Main Methods:

  • Measurement of blood glucose, plasma insulin, and plasma glucagon in portal and peripheral circulation.
  • Administration of an oral glucose and protein load (1 g/kg each) after a 4-hour fast.
  • Comparison of hormonal levels between SGA and AGA infants during the first 48 hours of life.

Main Results:

  • Fasting blood glucose was higher in the portal vein than the aorta in both SGA and AGA infants.
  • Both groups showed a significant rise in blood glucose after the nutrient load.
  • Insulin response to the load was minimal in SGA infants compared to AGA infants, with significant increases only observed in the portal vein of SGA infants.
  • Glucagon levels did not significantly rise in SGA infants after the load, unlike in AGA infants.
  • The insulin-to-glucagon molar ratio increased significantly in the portal vein of both groups after the load.
  • No significant differences in mean blood glucose, insulin, or glucagon levels were found between SGA and AGA infants when directly compared.

Conclusions:

  • SGA and AGA premature infants exhibit similar patterns of pancreatic hormone secretion in the initial days of life.
  • Despite some differences in response magnitude, the overall secretory capacity for insulin and glucagon appears comparable between SGA and AGA newborns.
  • These findings suggest that the endocrine pancreas functions similarly in both SGA and AGA infants during the early neonatal period.

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