Alternative Cerebral Fuels in the First Five Days in Healthy Term Infants: The Glucose in Well Babies (GLOW) Study
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Updated: Nov 23, 2025

Non-invasive Optical Measurement of Cerebral Metabolism and Hemodynamics in Infants
Published on: March 14, 2013
Deborah L Harris1, Philip J Weston2, Jane E Harding3
1Newborn Intensive Care Unit, Waikato District Health Board, Hamilton, New Zealand; Liggins Institute, University of Auckland, Auckland, New Zealand; School of Nursing, Midwifery and Health Practice, Victoria University of Wellington, Wellington, New Zealand.
Insights
In healthy infants, lactate and beta-hydroxybutyrate (BHB) are important cerebral fuels in the first 5 days. However, they are unlikely to offer neuroprotection during hypoglycemia.
Area of Science:
- Neonatal physiology
- Metabolic adaptation in newborns
Background:
- Infants undergo rapid metabolic changes after birth.
- Glucose is the primary energy source, but other fuels become important.
Purpose of the Study:
- To measure plasma lactate and beta-hydroxybutyrate (BHB) levels in healthy infants during the first 5 days of life.
- To investigate the relationship between these metabolites and glucose concentrations.
Main Methods:
- Prospective observational study of 67 healthy term infants in New Zealand.
- Collected heel-prick blood samples multiple times within the first 96 hours after birth.
Main Results:
- Plasma lactate was highest in the first 12 hours, decreasing thereafter. BHB levels were low initially, peaking at 48-72 hours.
- Lower glucose concentrations were associated with lower lactate and higher BHB levels.
- Glucose provided the majority of estimated ATP (72%-84%), with lactate and BHB contributing less.
Conclusions:
- Lactate and BHB may serve as cerebral fuels in healthy newborns.
- These metabolites are unlikely to provide neuroprotection during periods of hypoglycemia.
Objectives:
To determine plasma lactate and beta-hydroxybutyrate (BHB) concentrations of healthy infants in the first 5 days and their relationships with glucose concentrations.
Study Design:
Prospective masked observational study in Hamilton, New Zealand. Term, appropriately grown singletons had heel-prick blood samples, 4 in the first 24 hours then twice daily.
Results:
In 67 infants, plasma lactate concentrations were higher in the first 12 hours (median, 20; range, 10-55 mg/dL [median, 2.2 mmol/L; range, 1.1-6.2 mmol/L]), decreasing to 12 mg/dL (range, 7-29 mg/dL [median, 1.4 mmol/L; range, 0.8-3.3 mmol/L]) after 48 hours. Plasma BHB concentrations were low in the first 12 hours (median, 0.9 mg/dL; range, 0.5-5.2 mg/dL [median, 0.1 mmol/L; range, 0.05-0.5 mmol/L]), peaked at 48-72 hours (median, 7.3 mg/dL; range, 1.0-25.0 mg/dL [median, 0.7 mmol/L; range, 0.05-2.4 mmol/L]), and decreased by 96 hours (median, 0.9 mg/dL; range, 0.5-16.7 mg/dL [median, 0.1 mmol/L; range, 0.05-1.6 mmol/L]). Compared with infants with plasma glucose concentrations above the median (median, 67 mg/dL [median, 3.7 mmol/L]), those with lower glucose had lower lactate concentrations in the first 12 hours and higher BHB concentrations between 24 and 96 hours. Lower interstitial glucose concentrations were also associated with higher plasma BHB concentrations, but only if the lower glucose lasted greater than 12 hours. Glucose contributed 72%-84% of the estimated potential adenosine triphosphate throughout the 5 days, with lactate contributing 25% on day 1 and BHB 7% on days 2-3.
Conclusions:
Lactate on day 1 and BHB on days 2-4 may contribute to cerebral fuels in healthy infants, but are unlikely to provide neuroprotection during early or acute hypoglycemia.
Trial Registration:
The Australian and New Zealand Clinical Trials Registry: ACTRN12615000986572.
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