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Updated: Jun 2, 2026

Non-invasive Optical Measurement of Cerebral Metabolism and Hemodynamics in Infants
Published on: March 14, 2013
Change in mean transit time, apparent diffusion coefficient, and cerebral blood volume during pediatric diabetic
Monica S Vavilala1, Ken I Marro, Todd L Richards
1Department of Anesthesiology, University of Washington, Seattle, WA, USA. Vavilala@u.washington.edu
Insights
Cerebral edema in children with diabetic ketoacidosis may involve vasogenic changes. Mean transit time decreased and apparent diffusion coefficient increased during treatment, suggesting altered brain blood flow and water movement.
Area of Science:
- Pediatric neurology
- Neuroimaging
- Endocrinology
Background:
- Diabetic ketoacidosis (DKA) is a serious complication in children with diabetes.
- Cerebral edema is a life-threatening consequence of DKA, necessitating better understanding of its pathophysiology.
- Current understanding of brain changes during DKA treatment is limited.
Purpose of the Study:
- To investigate potential causes of whole brain and regional brain edema in children undergoing DKA treatment.
- To analyze changes in mean transit time (MTT), apparent diffusion coefficient (ADC), and relative cerebral blood volume (rCBV) during DKA management.
Main Methods:
- Prospective observational study conducted at a regional children's hospital.
- Serial contrast-enhanced and diffusion magnetic resonance imaging (MRI) scans were performed on children with DKA.
- Measurements of MTT, ADC, and rCBV were taken at two time points (12-24 hrs and 36-72 hrs) after initiating insulin therapy.
Main Results:
- Thirteen children with DKA were included in the study.
- Whole brain and regional mean transit time (MTT) significantly decreased by 51% (p = .01) between scans.
- Whole brain apparent diffusion coefficient (ADC) significantly increased by 4.7% (p = .001).
- No significant changes were observed in relative cerebral blood volume (rCBV).
Conclusions:
- The observed decrease in MTT and increase in ADC suggest a vasogenic process during DKA treatment.
- These findings may indicate changes in brain blood flow and water diffusion related to DKA management.
- Further research is needed to elucidate the precise mechanisms of cerebral edema in pediatric DKA.
Objectives:
Cerebral edema is a devastating complication of pediatric diabetic ketoacidosis. We examined measures describing potential causes of whole brain and regional brain edema (mean transit time, apparent diffusion coefficient, and relative cerebral blood volume) during treatment of diabetic ketoacidosis in children.
Design:
Prospective observational study.
Setting:
Regional children's hospital.
Interventions:
None.
Measurements And Main Results:
After Institutional Review Board approval, children admitted with diabetic ketoacidosis (pH <7.3, HCO3 <15 mEq/L, glucose >300 mg/dL, and ketosis) underwent two serial paired contrast-enhanced (gadolinium) and diffusion magnetic resonance imaging scans. Change in whole brain and regional (frontal lobe, occipital lobe, and basal ganglia) mean transit time, apparent diffusion coefficient, and relative cerebral blood volume between the two time periods (12-24 hrs) and (36-72 hrs) after start of insulin treatment (time 0) were determined. Thirteen children (median age, 10.3 ± 1.1 yrs; 7 female) with diabetic ketoacidosis were examined. Overall, whole brain and regional mean transit time decreased from time 1 (first magnetic resonance imaging after time 0) to time 2 (second magnetic resonance imaging after time 0) by 51% ± 59% (p = .01), without differences between the brain regions examined. Whole brain apparent diffusion coefficient increased by 4.7% ± 3.4% (p = .001), without differences between the brain regions examined. There was no change in relative cerebral blood volume for the whole brain and for the three brain regions examined.
Conclusions:
In this study, whole brain mean transit time decreased and apparent diffusion coefficient increased, suggesting a vasogenic process between the two study periods during diabetic ketoacidosis treatment.
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