Endogenous glucose production from infancy to adulthood: a non-linear regression model. Issue 12 (4th July 2014)

• Record Type: Journal Article
• Authors: Huidekoper, Hidde H; Ackermans, Mariëtte T; Ruiter, An F C; Sauerwein, Hans P; Wijburg, Frits A
• Is Part Of: Archives of disease in childhood. Volume 99:Issue 12(2014)
• Page Start: 1098
• Page End: 1102
• Publication Date: 2014-07-04
• Subjects: Paediatric Practice -- General Paediatrics -- Metabolic; Children -- Diseases -- Periodicals; Infants -- Diseases -- Periodicals; 618.920005
• DOI: 10.1136/archdischild-2013-305718
• Languages: English
• ISSNs: 0003-9888

Abstract

Abstract : Objective: To construct a regression model for endogenous glucose production (EGP) as a function of age, and compare this with glucose supplementation using commonly used dextrose-based saline solutions at fluid maintenance rate in children. Design: A model was constructed based on EGP data, as quantified by [6, 6- 2 H2 ] glucose dilution after fasting overnight during normoglycaemia, in 40 healthy subjects aged 2.5–54.3 years old. The data were analysed using non-linear regression modelling with a 1-phase exponential decay curve fit. This model was compared to the amount of glucose provided with 2.5% or 5% dextrose-based saline solutions infused at fluid maintenance rate. Results: Non-linear regression analysis of the EGP data yielded the following regression model: EGP (mg/kg/min) = 6.50 × 2.72 –0.145 × age (y) +1.93. Glucose supplementation at fluid maintenance rate with a 5% dextrose-based saline solution ranged from 46% at age 1 year to 55% at age 18 years of the glucose required to preclude the need for EGP. With a 2.5% dextrose-based solution, these percentages are 23% at age 1 year to 27% at age 18 years. Conclusions: we present an accurate non-linear regression model for EGP as a function of age. With standard dextrose-based saline solutions infused at fluid maintenance rate, only approximately 50% or less of EGP is provided. With prolonged infusion of these solutions, the deficit between exogenous glucose supplementation and EGP may induce a catabolic state and may ultimately lead to hypoglycaemia, especially in younger children.