Hyperglycaemic Preterm Babies Have Sex Differences in Insulin Secretion
Jennifer L Dickson1, J Geoffrey Chase, Christopher G Pretty
1Department of Mechanical Engineering, University of Canterbury, Christchurch, New Zealand.
Insights
Hyperglycaemia in preterm infants is linked to insulin secretion. This study found that insulin secretion increases with higher blood glucose levels and is greater in female infants.
Area of Science:
- Neonatalogy
- Endocrinology
- Metabolic Research
Background:
- Hyperglycaemia is a frequent complication in premature infants, contributing to mortality and morbidity.
- The exact causes of hyperglycaemia in neonates are not fully understood.
- Plasma C-peptide levels are used in adults to estimate insulin secretion due to predictable clearance.
Purpose of the Study:
- To quantify insulin secretion in hyperglycaemic preterm infants using plasma C-peptide concentrations.
- To investigate the relationship between blood glucose levels and endogenous insulin production in neonates.
- To explore potential sex-based differences in insulin secretion among preterm infants.
Main Methods:
- Retrospective analysis of 41 very preterm infants (median gestational age 27.2 weeks).
- Infants were enrolled in a trial for tight glycemic control upon developing hyperglycaemia (two consecutive blood glucose concentrations > 8.5 mmol·l⁻¹).
- Insulin secretion was calculated using a two-compartment C-peptide kinetic model with steady-state analysis.
Main Results:
- Blood glucose, insulin, C-peptide, and insulin secretion were higher at randomization compared to 1-2 weeks post-randomization.
- Female infants exhibited significantly higher insulin secretion (11.7 mU·l⁻¹·kg⁻¹·min⁻¹) than male infants (4.7 mU·l⁻¹·kg⁻¹·min⁻¹).
- Insulin secretion was lower during exogenous insulin administration compared to periods without it.
Conclusions:
- Endogenous insulin secretion in preterm infants is responsive to blood glucose levels.
- Female preterm infants demonstrate higher insulin secretion than males, independent of blood glucose and insulin concentrations.
- C-peptide analysis provides a valuable method for assessing insulin secretion in neonatal hyperglycaemia.
Background:
Hyperglycaemia is a common complication of prematurity and is associated with neonatal mortality and morbidity, yet the aetiology is incompletely understood. C-peptide has been used in adults to estimate endogenous insulin secretion due to its simple clearance kinetics.
Objective:
To determine insulin secretion calculated from plasma C-peptide concentrations in hyperglycaemic preterm babies.
Methods:
This is a retrospective analysis of a cohort of 41 very preterm babies with a median gestational age of 27.2 weeks (26.2-28.7) enrolled in a randomised controlled trial of tight glycaemic control when they developed hyperglycaemia (2 consecutive blood glucose concentrations, BGC, > 8.5 mmol·l(-1)). Insulin secretion was determined using a steady state analysis of a 2-compartment C-peptide kinetic model.
Results:
BGC, plasma insulin concentration, plasma C-peptide concentrations, and insulin secretion were higher at randomisation than 1-2 weeks following randomisation (p ≤ 0.02). Insulin secretion was higher in girls at 11.7 mU·l(-1)·kg(-1)·min(-1) (5.3-18.7) vs. 4.7 mU·l(-1)·kg(-1)·min(-1) (2.1-8.3; p < 0.005), with no difference in clinical characteristics, BGC, plasma insulin concentration, or nutrition between the sexes (p > 0.25). Insulin secretion was lower in samples taken during exogenous insulin delivery at 3.7 mU·l(-1)·kg(-1)·min(-1) (1.8-6.9) vs. 9.8 mU·l(-1)·kg(-1)·min(-1) (4.7-17.8; p = 0.02).
Conclusions:
Insulin secretion was higher when babies had higher BGC, indicating that endogenous insulin secretion is sensitive to BGC. Girls had higher insulin secretion, at similar blood glucose and plasma insulin concentrations, than boys.
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