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Characterization of Metabolic Status in Nonhuman Primates with the Intravenous Glucose Tolerance Test
Published on: November 13, 2016
Developmental disorders of glucose metabolism in infants
R Hume1, A McGeechan, A Burchell
1Department of Child Health, Obstetrics and Gynaecology, Tayside Institute of Child Health, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK. r.hume@dundee.ac.uk
Insights
Preterm infants show a significantly different response to glucagon tolerance tests compared to adults, indicating potential challenges in regulating blood glucose levels. This study adapted the test for neonates, revealing an attenuated glucose increase, likely due to lower hepatic glucose-6-phosphatase activity.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Pediatric Metabolism
Background:
- Postnatal blood glucose control is a common challenge in newborns, persisting for months.
- The glucagon tolerance test is the standard method for assessing hepatic glucose production.
Purpose of the Study:
- To adapt the standard glucagon tolerance test for use in preterm infants.
- To evaluate the glucose response to glucagon in preterm infants.
Main Methods:
- Adapted the standard glucagon tolerance test for preterm infants.
- Recruited 79 preterm infants (25-36 weeks gestational age) admitted to the Neonatal Intensive Care Unit.
- Administered the test at discharge home.
Main Results:
- The maximal plasma glucose increase in preterm infants was 1.39 +/- 0.07 mmol/L (range 0-3.98 mmol/L).
- This response is significantly lower than the abnormal threshold of <4 mmol/L seen in adults.
Conclusions:
- Preterm infants exhibit an attenuated response to glucagon compared to adults.
- This difference is likely due to lower hepatic glucose-6-phosphatase activity in preterm infants.
- Hepatic glucose-6-phosphatase is crucial for liver glucose production pathways.
Background:
Developmental failures to adequately control postnatal blood glucose levels are common in the transition from fetal to infant life and can persist for many months. The standard method of functionally measuring hepatic glucose production and/or disordered glucose production is the response to a glucagon tolerance test.
Method:
We adapted the standard glucagon tolerance test used for children and adults for use in preterm infants. 79 consecutive preterm infants gestational age range 25-36 weeks (mean 32.2 weeks), mean birth weight 1.66 kg admitted to the Neonatal Intensive Care Unit, Ninewells Hospital, Dundee and who survived to discharge home were recruited into the study. At the time of discharge home the characteristics of the group were as follows: adjusted mean gestational age 36.7 weeks, mean discharge weight 2.23 kg.
Results:
In this study of preterm infants the maximal increase in plasma glucose following administration of a glucagon tolerance test is 1.39 +/- 07 mmol/L, n = 78 (range 0-3.98 mmol/L).
Conclusions:
An increase in plasma glucose of less than 4 mmol/L is considered abnormal in adults following administration of a fasting glucagon tolerance test. The responses of preterm infants and adults to glucagon are clearly different. The attenuated response to glucagon in the preterm infants is consistent with the low levels of hepatic glucose-6-phosphatase activity in premature infants as glucose-6-phosphatase is the terminal step of the two main pathways of liver glucose production.
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