|Institution:||University of Canterbury|
|Keywords:||Glycaemic control; insulin therapy; insulin secretion; physiological modeling; very preterm infants; Field of Research::09 - Engineering::0903 - Biomedical Engineering; Field of Research::11 - Medical and Health Sciences::1103 - Clinical Sciences::110310 - Intensive Care; Field of Research::11 - Medical and Health Sciences::1103 - Clinical Sciences::110306 - Endocrinology|
|Full text PDF:||http://hdl.handle.net/10092/11824|
Background: Model-based glycaemic control relies on sufficiency of underlying models to describe underlying patient physiology. In particular, very preterm infant glucose-insulin metabolism can differ significantly from adults, and is relatively unstudied. In this study, C-peptide concentrations are used to develop insulin-secretion models for the purposes of glycaemic control in neonatal intensive care. Methods: Plasma C-peptide, Insulin, and blood glucose concentrations (BGC) were retrospectively analyzed from a cohort of 41 hyperglycemic very preterm (median age 27.2 [26.2 - 28.7] weeks) and very low birth-weight infants (median birth weight 839 [735 – 1000] g). A 2-compartment model of C-peptide kinetics was used to estimate insulin secretion. Insulin secretion was examined with respect to nutritional intake, exogenous and plasma insulin concentration, and BGC. Results: Insulin secretion was found to be highly variable between patients and over time, and could not be modeled with respect to age, weight, or protein or dextrose intake. In 13 of 54 samples exogenous insulin was being administered, and insulin secretion was lower. However, low data numbers make this result inconclusive. Insulin secretion was found to increase with BG, with a stronger association in female infants than males (R2=0.51 vs. R2=0.13, and R2=0.26 for the combined cohort). Conclusions: A sex-based insulin secretion model was created and incorporated into a model-based glycemic control framework. Nutritional intake did not predict insulin secretion, indicating that insulin secretion is a complex function of a number of metabolic factors.