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Updated: Aug 13, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Estimation of gluconeogenesis in newborn infants
S C Kalhan1, P Parimi, R Van Beek
1Schwartz Center for Metabolism and Nutrition, MetroHealth Medical Center, Case Western Reserve University School of Medicine, Cleveland, Ohio 44109, USA. sck@po.cwru.edu
Insights
Newborn infants show significant gluconeogenesis (GNG) soon after birth. This process, particularly via pyruvate, contributes substantially to glucose production, impacting nutritional support strategies for healthy and sick newborns.
Area of Science:
- Neonatal Metabolism
- Pediatric Endocrinology
- Biochemistry
Background:
- Glucose homeostasis is critical in newborns.
- Understanding gluconeogenesis (GNG) in neonates is essential for nutritional support.
- Limited data exists on early GNG contributions in low-birth-weight and term infants.
Purpose of the Study:
- To quantify glucose turnover and GNG rates in term and preterm infants.
- To assess the contribution of pyruvate and lactate to glucose production in newborns.
- To evaluate the impact of parenteral nutrition on GNG in preterm infants.
Main Methods:
- Utilized stable isotope tracers [(13)C(6)]glucose and (2)H(2)O to measure glucose rate of appearance (R(a)) and GNG.
- Measured lactate turnover and its incorporation into glucose using [(13)C(3)]lactate tracer.
- Analyzed infants at different postnatal ages and nutritional support conditions.
Main Results:
- Term infants (24-48h) showed glucose R(a) of 30 ± 1.7 µmol·kg⁻¹·min⁻¹, with GNG via pyruvate contributing ~31%.
- Preterm infants exhibited variable GNG contributions (6-60%), highest with low exogenous glucose infusion.
- Lactate contributed ~18% to glucose production in neonates within 4-24h of birth.
Conclusions:
- Gluconeogenesis is active early in neonatal life.
- Pyruvate is a significant substrate for GNG in healthy term infants, even after short fasting periods.
- Findings have implications for optimizing nutritional management in sick and healthy neonates.
Abstract:
The rate of glucose turnover (R(a)) and gluconeogenesis (GNG) via pyruvate were quantified in seven full-term healthy babies between 24 and 48 h after birth and in twelve low-birth-weight infants on days 3 and 4 by use of [(13)C(6)]glucose and (2)H(2)O. The preterm babies were receiving parenteral alimentation of either glucose or glucose plus amino acid with or without lipids. The contribution of GNG to glucose production was measured by the appearance of (2)H on C-6 of glucose. Glucose R(a) in full-term babies was 30 +/- 1.7 (SD) micromol. kg(-1). min(-1). GNG via pyruvate contributed approximately 31% to glucose R(a). In preterm babies, the contribution of GNG to endogenous glucose R(a) was variable (range 6-60%). The highest contribution was in infants receiving low rates of exogenous glucose infusion. In an additional group of infants of normal and diabetic mothers, lactate turnover and its incorporation into glucose were measured within 4-24 h of birth by use of [(13)C(3)]lactate tracer. The rate of lactate turnover was 38 micromol. kg(-1). min(-1), and lactate C, not corrected for loss of tracer in the tricarboxylic acid cycle, contributed approximately 18% to glucose C. Lactate and glucose kinetics were similar in infants that were small for their gestational age and in normal infants or infants of diabetic mothers. These data show that gluconeogenesis is evident soon after birth in the newborn infant and that, even after a brief fast (5 h), GNG via pyruvate makes a significant contribution to glucose production in healthy full-term infants. These data may have important implications for the nutritional support of the healthy and sick newborn infant.
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