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Updated: May 27, 2026

A Behavioral Screen for Heat-Induced Seizures in Mouse Models of Epilepsy
Published on: July 12, 2021
S100B proteins in febrile seizures
Kirsi Mikkonen1, Niina Pekkala, Tytti Pokka
1Department of Pediatrics, University of Oulu, P.O. Box 5000, FIN-90014 University of Oulu, Finland. kirsi.mikkonen@oulu
Febrile seizures (FS) in children do not significantly increase S100B protein levels, suggesting no major blood-brain barrier damage. This indicates that these common childhood seizures are generally harmless to brain development.
Area of Science:
- Pediatric Neurology
- Biomarkers
- Neuroscience
Background:
- S100B protein is a marker for brain damage and blood-brain barrier integrity.
- Elevated S100B in children can indicate astrocyte damage, even after mild head injuries.
- S100B may reflect ongoing brain pathology in febrile seizures (FS) and recurrence risk.
Purpose of the Study:
- To evaluate S100B protein concentrations in serum and cerebrospinal fluid after a child's first febrile seizure.
- To determine if S100B levels correlate with FS severity or recurrence.
- To assess if FS causes significant blood-brain barrier opening.
Main Methods:
- Measured S100B protein concentrations in serum and cerebrospinal fluid of 103 children post-first FS.
- Included 33 children with acute infection but no FS as controls for serum S100B.
- Analyzed correlations between S100B levels, age, time to hospital, FS severity, and recurrence.
Main Results:
- Mean serum S100B was 0.12 μg/L in FS patients and 0.11 μg/L in controls (P=0.46).
- Mean cerebrospinal fluid S100B was 0.21 μg/L in FS patients.
- S100B concentrations did not predict FS severity or recurrence; no correlation with time to hospital.
Conclusions:
- Febrile seizures (FS) in children do not appear to cause significant blood-brain barrier disruption.
- Findings support the notion that FS are relatively benign for the developing brain.
- S100B protein levels are not predictive of FS severity or recurrence in this cohort.
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