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Updated: Jan 24, 2026

Isolation and Cannulation of Cerebral Parenchymal Arterioles
Published on: May 23, 2016
Enteroviral meningitis reduces CSF concentration of Aβ42, but does not affect markers of parenchymal damage
Kacper Toczylowski1, Malgorzata Wojtkowska2, Artur Sulik3
1Department of Pediatric Infectious Diseases, Medical University of Bialystok, Waszyngtona 17, 15-274, Bialystok, Poland.
Abstract:
Biomarkers classically studied in Alzheimer's disease have been analyzed in numerous central nervous system infections in adults, but there are scarce data on these biomarkers in children. Enteroviruses appear to be the most common cause of aseptic meningitis throughout the world. The aim of the study was to investigate neuroinflammatory properties of non-polio enteroviruses by measuring CSF concentrations of biomarkers that are involved in neuropathological pathways of neurodegenerative disorders. We measured Aβ42, t-tau, and S100B concentrations in 42 children with enteroviral meningitis (EM) compared to control group without central nervous system infection. We found enteroviral meningitis (EM) to reduce CSF concentration of Aβ42 (median, 1051.1 pg/mL; interquartile range (IQR), 737.6-1559.5 vs. median, 459.4 pg/mL; IQR, 312.0-662.0, p < 0.001). In contrast, CSF concentrations of t-tau and S100B were not affected by EM. There was a correlation between total neutrophil count in CSF and Aβ42 (R = - 0.59, p < 0.001). Absolute number of mononuclear cells in the CSF correlated with CSF t-tau (R = 0.41, p < 0.05). Both correlations remained significant after adjustment for age, blood leukocytes, serum CRP, CSF leukocytes, and CSF protein concentration.
Insights
Enteroviral meningitis in children significantly lowers cerebrospinal fluid amyloid-beta 42 (Aβ42) levels. Cerebrospinal fluid concentrations of tau (t-tau) and S100B were unaffected by enteroviral meningitis.
Area of Science:
- Pediatric Neurology
- Neurovirology
- Neuroinflammation
Background:
- Alzheimer's disease biomarkers are studied in adult CNS infections, but data in children are limited.
- Enteroviruses are a common cause of aseptic meningitis globally.
- Investigating neuroinflammatory markers in pediatric CNS infections is crucial.
Purpose of the Study:
- To examine the neuroinflammatory impact of non-polio enteroviruses in children.
- To measure cerebrospinal fluid (CSF) concentrations of Alzheimer's-associated biomarkers (Aβ42, t-tau, S100B) in pediatric enteroviral meningitis (EM).
- To explore correlations between inflammatory cell counts and biomarker levels in pediatric EM.
Main Methods:
- Analyzed CSF samples from 42 children diagnosed with enteroviral meningitis (EM) and a control group.
- Measured concentrations of amyloid-beta 42 (Aβ42), total tau (t-tau), and S100B using standard assays.
- Correlated CSF biomarker levels with neutrophil and mononuclear cell counts, adjusting for confounding factors.
Main Results:
- EM significantly reduced CSF Aβ42 levels compared to controls (p < 0.001).
- CSF concentrations of t-tau and S100B remained unaffected by EM.
- CSF neutrophil count correlated negatively with Aβ42 (R = -0.59, p < 0.001).
- CSF mononuclear cell count correlated positively with t-tau (R = 0.41, p < 0.05).
Conclusions:
- Pediatric enteroviral meningitis alters CSF Aβ42 levels, suggesting a potential link to neurodegenerative pathways.
- Inflammatory responses in pediatric EM are associated with specific CSF biomarker changes.
- Further research is needed to understand the long-term neurological implications of these biomarker alterations in children.
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