1. Biomarkers and genotypes in patients with Central nervous system infection caused by enterovirus.
- Author
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Alsén K, Patzi Churqui M, Norder H, Rembeck K, Zetterberg H, Blennow K, Sahlgren F, and Grahn A
- Subjects
- Humans, Male, Female, Retrospective Studies, Adult, Middle Aged, Adolescent, Child, Genotype, S100 Calcium Binding Protein beta Subunit cerebrospinal fluid, Child, Preschool, Young Adult, Neurofilament Proteins cerebrospinal fluid, Central Nervous System Infections cerebrospinal fluid, Central Nervous System Infections virology, Aged, Infant, Peptide Fragments cerebrospinal fluid, Peptide Fragments blood, Biomarkers cerebrospinal fluid, Enterovirus genetics, Enterovirus isolation & purification, Enterovirus Infections cerebrospinal fluid, Enterovirus Infections virology, tau Proteins cerebrospinal fluid, Amyloid beta-Peptides cerebrospinal fluid, Glial Fibrillary Acidic Protein cerebrospinal fluid
- Abstract
Purpose: Enteroviruses (EV) comprises many different types and are the most common cause of aseptic meningitis. How the virus affects the brain including potential differences between types are largely unknown. Measuring biomarkers in CSF is a tool to estimate brain damage caused by CNS infections., Methods: A retrospective study was performed in samples from 38 patients with acute neurological manifestations and positive CSF-EV RNA ( n = 37) or serum-IgM ( n = 1). The EV in 17 samples were typed by sequencing. The biomarkers neurofilament light (NFL), glial fibrillary acidic protein (GFAP), S-100B protein, amyloid-β (Aβ) 40 and Aβ42, total-tau (T-tau) and phosphorylated tau (P-tau) were measured and compared with data derived from a control group ( n = 19)., Results: There were no increased levels of GFAP ( p ≤ 0.1) nor NFL ( p ≤ 0.1) in the CSF of patients with EV meningitis ( n = 38) compared with controls. However, we found decreased levels of Aβ42 ( p < 0.001), Aβ40 ( p < 0.001), T-tau ( p ≥ 0.01), P-tau ( p ≤ 0.001) and S-100B ( p ≤ 0.001). E30 ( n = 9) and CVB5 ( n = 6) were the most frequent EV-types identified, but no differences in biomarker levels or other clinical parameters were found between the infecting virus type. Seven patients who were followed for longer than one month reported remaining cognitive impairment, although no correlations with biomarker concentrations were observed., Conclusion: There are no indication of neuronal or astrocyte damage in patients with EV meningitis. Yet, decreased concentrations of Aβ40, Aβ42, P-tau and T-tau were shown, a finding of unknown importance. Cognitive impairment after acute disease occurs, but with only a limited number of patients analysed, no conclusion can be drawn concerning any association with biomarker levels or EV types.
- Published
- 2024
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