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Transient neonatal hyperinsulinism: early predictors of duration
Shai Fuchs1,2, Ravit Regev1, Jennifer Harrington1
1Division of Endocrinology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Insights
Early glucose trends in infants with transient hyperinsulinism (tHI) may predict disease duration. Fetal distress is linked to shorter tHI resolution, suggesting a distinct clinical course.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Pediatrics
Background:
- Transient hyperinsulinism (tHI) is a common cause of infant hypoglycemia.
- Predicting tHI severity and resolution time is currently challenging.
- Early identification of disease duration is crucial for infant care.
Purpose of the Study:
- To determine if early glucose trends predict disease duration in infants with tHI.
- To identify potential predictors for tHI resolution time.
Main Methods:
- Retrospective pilot cohort study of neonates with tHI.
- Phenotyping for clinical and laboratory parameters.
- Collection of blood glucose values for 120 hours post-hypoglycemia diagnosis.
Main Results:
- Higher mean daily glucose and fetal distress were associated with shorter tHI duration.
- In neonates without fetal distress, lower mean daily glucose correlated with longer disease duration.
- Pilot data suggests early predictors for tHI duration exist within the first week.
Conclusions:
- Early glucose trends in the first week of life may predict tHI duration.
- tHI associated with fetal distress might be a distinct entity with a shorter clinical course.
Objectives:
Hyperinsulinism is the most common cause of recurrent hypoglycemia in infants, with transient and permanent forms. Currently, there are no effective tools to predict severity and time to resolution in infants with transient hyperinsulinism (tHI). Therefore, our objective was to assess whether early glucose trends predict disease duration in tHI.
Methods:
A retrospective, pilot cohort of infants admitted with tHI was phenotyped for clinical and laboratory parameters. Blood glucose (BG) values were collected from the first documented hypoglycemia for 120 h (five days).
Results:
In 27 neonates with tHI, the presence of fetal distress (p=0.001) and higher mean daily BG (p=0.035) were associated with shorter time to resolution of hypoglycemia. In a further sensitivity analysis that grouped the cohort by the presence or absence of fetal distress, we found that in neonates without fetal distress, lower mean daily glucose was associated with longer disease duration (R2=0.53, p=0.01).
Conclusions:
Our pilot data suggests that predictors for disease duration of tHI may be elicited in the first week of life, and that tHI associated with fetal distress may represent a distinct clinical entity with a shorter time course.
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