Literature DB >> 2118616

Glucose production and oxidation in preterm infants during total parenteral nutrition.

H N Lafeber1, E J Sulkers, T E Chapman, P J Sauer.   

Abstract

During total parenteral nutrition in preterm infants, glucose may be infused at high rates, but it is not known if the endogenous glucose production is fully suppressed under these circumstances. Eight preterm appropriate for gestational age (AGA) (birth wt: 1613 +/- 151 g, gestational age: 31.1 +/- 1.5 wk) and eight preterm small for gestational age (SGA) newborn infants (1185 +/- 241 g, 32.9 +/- 2.6 wk) receiving a glucose infusion rate of 7.55 +/- 0.56 and 8.16 +/- 0.65 mg/kg.min, respectively, were studied during continuous total parenteral nutrition at postnatal d 8. Glucose oxidation rate was determined with a primed constant infusion of [U-13C] glucose, measuring the 13CO2 production in breath gas by isotope ratio mass spectrometry and the glucose production rate in plasma by gas chromatography mass spectrometry. In breath gas of AGA and SGA infants, 60 and 65%, respectively, of the infused tracer appeared as 13CO2. The glucose production rates were 7.97 +/- 1.61 and 8.12 +/- 1.84 mg/kg.min in AGA and SGA infants, respectively, indicating that no significant endogenous glucose production occurred. The glucose oxidation calculated from the glucose production and 13CO2 production was 4.74 +/- 0.99 mg/kg.min in AGA infants and was significantly different from the carbohydrate oxidation rate of 6.62 +/- 1.23 mg/kg.min measured by simultaneous indirect calorimetry. In SGA infants, however, the glucose and carbohydrate oxidation rates were not significantly different at 5.33 +/- 1.56 and 6.16 +/- 2.45 mg/kg.min. It is concluded that 1-wk-old AGA or SGA preterm infants receiving total parenteral nutrition of 80 kcal/kg.d produce no endogenous glucose and their glucose oxidation rates are similar at 63-65% of the glucose infused. It is suggested that the significant difference between glucose and carbohydrate oxidation rates observed in AGA but not in SGA infants is due either to a higher rate of lipogenesis from carbohydrates, or, less likely, to a higher rate of glycogen oxidation.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2118616     DOI: 10.1203/00006450-199008000-00015

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  3 in total

1.  Glucose metabolism in a term infant with transient hyperinsulinism and high carbohydrate intake.

Authors:  J B van Goudoever; E J Sulkers; S C Kalhan; P J Sauer
Journal:  Eur J Pediatr       Date:  1993-04       Impact factor: 3.183

Review 2.  Neonatology/Paediatrics - Guidelines on Parenteral Nutrition, Chapter 13.

Authors:  C Fusch; K Bauer; H J Böhles; F Jochum; B Koletzko; M Krawinkel; K Krohn; S Mühlebach
Journal:  Ger Med Sci       Date:  2009-11-18

3.  Standardised neonatal parenteral nutrition formulations - an Australasian group consensus 2012.

Authors:  Srinivas Bolisetty; David Osborn; John Sinn; Kei Lui
Journal:  BMC Pediatr       Date:  2014-02-18       Impact factor: 2.125

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.