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A Piglet Model of Neonatal Hypoxic-Ischemic Encephalopathy
Published on: May 16, 2015
Early Glycemic Profile Is Associated with Brain Injury Patterns on Magnetic Resonance Imaging in Hypoxic Ischemic
Sudeepta K Basu1, Katherine Ottolini1, Vedavalli Govindan2
1Division of Neonatology, Children's National Health System, Washington, DC.
Insights
Infants with hypoxic ischemic encephalopathy (HIE) and abnormal early blood glucose levels show distinct patterns of brain injury on MRI. These glycemic profiles may serve as biomarkers for predicting injury severity in HIE.
Area of Science:
- Neonatal neurology
- Pediatric critical care
- Neuroimaging
Background:
- Hypoxic ischemic encephalopathy (HIE) is a major cause of neonatal brain injury.
- Therapeutic hypothermia is the standard treatment for HIE.
- Early glycemic dysregulation is common in HIE but its association with brain injury patterns is not well-defined.
Purpose of the Study:
- To investigate the association between early glycemic profiles and specific patterns of brain injury in infants with HIE.
- To determine if glycemic status can predict neuroimaging findings in HIE.
Main Methods:
- Secondary analysis of 178 infants with HIE treated with therapeutic hypothermia.
- Classification of glycemic profiles: normoglycemia, hypoglycemia, hyperglycemia, and labile glucose within 24 hours of birth.
- Assessment of brain injury patterns using Barkovich scores on MRI in 151 infants.
Main Results:
- Infants with abnormal glucose profiles had a higher likelihood of abnormal brain MRIs compared to those with normoglycemia (32% vs. 60%).
- Hypoglycemia and labile glucose were associated with increased odds of watershed or focal-multifocal injury.
- Labile glucose was linked to a higher likelihood of basal ganglia or global brain injury.
Conclusions:
- Early glycemic profiles in infants with HIE are significantly associated with distinct patterns of brain injury on MRI.
- Glycemic status may serve as a potential biomarker for predicting neuroimaging outcomes in HIE.
- Further research is warranted to explore the prognostic significance of these findings.
Objective:
To investigate whether the early glycemic profile in infants with hypoxic ischemic encephalopathy is associated with distinct patterns of brain injury on magnetic resonance imaging (MRI).
Study Design:
We performed a secondary analysis of 178 prospectively enrolled infants who received therapeutic hypothermia for hypoxic ischemic encephalopathy. Glycemic profiles were identified by glucose concentrations within 24 hours after birth: normoglycemia (all glucose concentrations of >47 to ≤150 mg/dL; n = 62); hypoglycemia (≥1 concentration ≤47 mg/dL; n = 17); hyperglycemia (≥1 concentration >150 mg/dL; n = 76); and labile glucose (both hypoglycemia and hyperglycemia; n = 23). Patterns of brain injury were identified for 151 infants based on Barkovich scores from the postrewarming brain MRIs at a median age of 9 days.
Results:
A normal brain MRI was reported in 37 of 62 infants (60%) with normal blood glucose values compared with 37 of 116 infants (32%) with an abnormal glucose profile (adjusted for Sarnat stage of encephalopathy and Apgar score at 5 minutes; P = .02). The distribution of MRI patterns of brain injury differed among the glycemic groups (P = .03). The odds of predominant watershed or focal-multifocal injury was higher in infants with hypoglycemia (aOR, 6; 95% CI, 1.5-24.2) and labile glucose (6.6; 95% CI, 1.6-27) compared with infants with normoglycemia. Infants with labile glucose had higher odds (5.6; 95% CI, 1.1-29.3) of predominant basal ganglia or global injury compared with infants with normal blood glucose values.
Conclusions:
The early glycemic profile in infants with hypoxic ischemic encephalopathy is associated with specific patterns of brain injury on MRI. Further investigation is needed to explore its prognostic significance and role as a phenotype biomarker.
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