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.
Abstract

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