Archives of disease in childhood. Fetal and neonatal edition · 2016
Insulin resistance, glucagon-like peptide-1 and factors influencing glucose homeostasis in neonates.
СтатьяНаблюдательное исследованиеНазвание и аннотация: Перевод в очереди
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Salis Emma R, Reith David M, Wheeler Benjamin J, Broadbent Roland S, Medlicott Natalie J
Аннотация
OBJECTIVES: To explore the relationships between postmenstrual age (PMA), insulin, C-peptide, glucagon and blood glucose concentrations (BGCs) in preterm and term neonates. To compare glucagon-like peptide-1 (GLP-1) concentrations in fed versus never-fed neonates.
DESIGN: Observational.
SETTING: Dunedin Hospital Neonatal Intensive Care Unit, New Zealand.
PATIENTS: Term or preterm euglycaemic neonates (102) receiving routine blood tests (343 samples).
INTERVENTIONS: None: plasma was obtained from surplus samples from routine clinical care.
MAIN OUTCOME MEASURES: Insulin, C-peptide, GLP-1 and glucagon concentrations were measured in temporal association with BGC.
RESULTS: Insulin and C-peptide concentrations were elevated in very preterm infants (PMA≤32 weeks) and decreased to term; this relationship persisted when BGCs were accounted for. Generalised linear mixed models showed that insulin:C-peptide ratio and insulin:BGC ratio decreased significantly with increasing PMA (p<0.001). GLP-1 increased following initial oral feeds regardless of PMA (p<0.001).
CONCLUSION: Preterm neonates exhibit insulin resistance in the absence of hyperglycaemia. Enteral feeds result in an increase in GLP-1. These factors are likely to contribute to the increased risk of hyperglycaemia in premature neonates (PMA<32 weeks).
DESIGN: Observational.
SETTING: Dunedin Hospital Neonatal Intensive Care Unit, New Zealand.
PATIENTS: Term or preterm euglycaemic neonates (102) receiving routine blood tests (343 samples).
INTERVENTIONS: None: plasma was obtained from surplus samples from routine clinical care.
MAIN OUTCOME MEASURES: Insulin, C-peptide, GLP-1 and glucagon concentrations were measured in temporal association with BGC.
RESULTS: Insulin and C-peptide concentrations were elevated in very preterm infants (PMA≤32 weeks) and decreased to term; this relationship persisted when BGCs were accounted for. Generalised linear mixed models showed that insulin:C-peptide ratio and insulin:BGC ratio decreased significantly with increasing PMA (p<0.001). GLP-1 increased following initial oral feeds regardless of PMA (p<0.001).
CONCLUSION: Preterm neonates exhibit insulin resistance in the absence of hyperglycaemia. Enteral feeds result in an increase in GLP-1. These factors are likely to contribute to the increased risk of hyperglycaemia in premature neonates (PMA<32 weeks).