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Serum and cerebrospinal fluid phosphorylated neurofilament heavy subunit as a marker of neuroaxonal damage in tick-borne encephalitis

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    SYSNO ASEP0557775
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSerum and cerebrospinal fluid phosphorylated neurofilament heavy subunit as a marker of neuroaxonal damage in tick-borne encephalitis
    Author(s) Fořtová, A. (CZ)
    Hönig, Václav (BC-A) RID, ORCID
    Palus, Martin (BC-A) RID, ORCID
    Salát, Jiří (BC-A) RID, ORCID
    Pychova, M. (CZ)
    Krbková, L. (CZ)
    Vyhlídalová, Tereza (BC-A) ORCID
    Kříha, M. (CZ)
    Chrdle, A. (CZ)
    Růžek, Daniel (BC-A) RID, ORCID
    Number of authors10
    Article number001743
    Source TitleJournal of General Virology. - : Microbiology Society - ISSN 0022-1317
    Roč. 103, č. 5 (2022)
    Number of pages7 s.
    Publication formOnline - E
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsvirus rna ; chemokines ; identification ; infection ; diagnosis ; cxcl10 ; tick-borne encephalitis ; neurofilament ; brain injury ; biomarker ; flavivirus
    Subject RIVEE - Microbiology, Virology
    OECD categoryVirology
    R&D ProjectsGA20-14325S GA ČR - Czech Science Foundation (CSF)
    GA20-30500S GA ČR - Czech Science Foundation (CSF)
    Method of publishingLimited access
    Institutional supportBC-A - RVO:60077344
    UT WOS000798232700001
    EID SCOPUS85129429737
    DOI10.1099/jgv.0.001743
    AnnotationExtensive axonal and neuronal loss is the main cause of severe manifestations and poor outcomes in tick-borne encephalitis (TBE). Phosphorylated neurofilament heavy subunit (pNF-H) is an essential component of axons, and its detection in cerebrospinal fluid (CSF) or serum can indicate the degree of neuroaxonal damage. We examined the use of pNF-H as a biomarker of neuroaxonal injury in TBE. In 89 patients with acute TBE, we measured CSF levels of pNF-H and 3 other markers of brain injury (glial fibrillary acidic protein, S100B and ubiquitin C-terminal hydrolase L1) and compared the results to those for patients with meningitis of other aetiology and controls. Serum pNF-H levels were measured in 80 patients and compared with findings for 90 healthy blood donors. TBE patients had significantly (P<0.001) higher CSF pNF-H levels than controls as early as hospital admission. Serum pNF-H concentrations were significantly higher in samples from TBE patients collected at hospital discharge (P<0.0001) than in controls. TBE patients with the highest peak values of serum pNF-H, exceeding 10000 pg ml(-1), had a very severe disease course, with coma or tetraplegia. Patients requiring intensive care had significantly higher serum pNF-H levels than other TBE patients (P<0.01). Elevated serum pNF-H values were also observed in patients with incomplete recovery (P<0.05). Peak serum pNF-H levels correlated positively with the duration of hospitalization (P=0.005). Measurement of pNF-H levels in TBE patients might be useful for assessing disease severity and determining prognosis.
    WorkplaceBiology Centre (since 2006)
    ContactDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Year of Publishing2023
    Electronic addresshttps://www.microbiologyresearch.org/content/journal/jgv/10.1099/jgv.0.001743
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