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Published on: June 21, 2019
Prognostic value of brain injury biomarkers in acute encephalitis/encephalopathy
Hirokazu Tsukahara1, Yosuke Fujii, Kousaku Matsubara
1Department of Pediatrics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan. hirokazu010661@yahoo.co.jp
Insights
Biomarkers like S-100B and tau in cerebrospinal fluid can predict poor outcomes in children with acute encephalitis/encephalopathy (AEE). Combined assessment of these brain injury markers offers high accuracy for predicting clinical outcomes in pediatric AEE.
Area of Science:
- Pediatric Neurology
- Neuroscience
- Biomarker Discovery
Background:
- Acute encephalitis/encephalopathy (AEE) is a severe condition in children, often leading to significant neurodevelopmental issues or death.
- Predicting outcomes in pediatric AEE is crucial for timely intervention and management.
- Bedside point-of-care testing for ongoing brain injury is highly desirable.
Purpose of the Study:
- To evaluate the potential of specific brain injury markers in cerebrospinal fluid (CSF) to predict outcomes in children with AEE.
- To compare the predictive accuracy of S-100B, glial fibrillary acidic protein (GFAP), and tau protein levels in CSF for AEE outcomes.
Main Methods:
- CSF samples were collected from children diagnosed with AEE and controls.
- Three groups were analyzed: non-AEE controls, AEE with mild sequelae, and AEE with severe sequelae or death.
- Levels of S-100B, GFAP, and tau protein were measured in early CSF samples.
Main Results:
- All three markers (S-100B, GFAP, tau) were significantly elevated in children with AEE and poor outcomes compared to controls and those with mild sequelae.
- A scoring system combining S-100B and tau levels achieved 100% accuracy in identifying poor outcomes in pediatric AEE patients.
- Individual markers also showed significant predictive accuracy, with S-100B at 91% and tau at 78% for poor outcomes.
Conclusions:
- Combined measurement of S-100B and tau in CSF shows strong promise for predicting clinical outcomes in children with AEE.
- These biomarkers may facilitate early identification of children at risk for severe sequelae or death from AEE.
- Scoring assessments based on these CSF markers could become valuable tools for bedside prognostication in pediatric neurology.
Background:
Acute encephalitis/encephalopathy (AEE) is a devastating cause of severe neurodevelopmental sequelae or death in children. Assessing ongoing brain injury and predicting outcomes using bedside point-of-care testing is expected to be extremely valuable.
Methods:
For this study, three brain injury markers, S-100B, glial fibrillary acidic protein (GFAP), and tau protein, were measured in early cerebrospinal fluid samples of children with AEE. Subjects comprised three groups: Group 1 (non-AEE control, n = 27); Group 2 (AEE with normal resolution or mild sequelae, n = 13); and Group 3 (AEE with severe sequelae or death, i.e. "poor outcome," n = 10).
Results:
All marker levels were significantly higher in Group 3 than in Group 1 or 2. In Group 3, only S-100B was significantly higher in non-survivors than in survivors. For scoring assessment (range: 0-3 points), the predictive accuracies of 3 points for poor outcomes in children with AEE (i.e. Group 2 and 3, n = 23) were 91% (21/23) for S-100B, 74% (17/23) for GFAP, and 78% (18/23) for tau. When the scores were summed up for S-100B, GFAP, and tau (range: 0-9 points), and for S-100B and tau (range: 0-6 points), the patients with poor outcomes were identified more accurately using the respective thresholds of 6 points and 4 points (96% [22/23] and 100% [23/23], respectively).
Conclusion:
Our findings suggest that combined measurement and scoring assessment of the markers, especially S-100B and tau, show promise as predictors of clinical outcomes in children with AEE.
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