COVID-19 patients had higher levels of IL-18, IL-6, and IL-8 in both serum and CSF, MCP1 was elevated only in CSF, while IL-10, IL-1RA, IP-10, MIG and NfL were increased only in serum. No differences were found between patients with encephalitis and encephalopathy. 14-3-3, NfL, IL-18, IL-1RA and IL-8 significantly correlated with acute COVID-19 severity, measured as mild (without oxygen supplementation), moderate (oxygen), and severe (assisted ventilation). At 18 months, only levels of 14-3-3 and NfL in CSF significantly correlated with neurologic disability measured by the Modified Rankin Scale. G-CSF, IL-17a, IL-1b, IFN-γ, MCP3 and TNF-α and antibodies against neural antigens were undetectable or negligible in the serum and CSF in healthy controls and COVID-19 patients. The authors conclude that while there is an inflammatory response in these patients, only markers of neuronal damage predict long-term functional outcome.
Guasp M, Muñoz-Sánchez G, Martínez-Hernández E, Santana D, Carbayo Á, Naranjo L, Bolós U, Framil M, Saiz A, Balasa M, Ruiz-García R, Sánchez-Valle R and The Barcelona Neuro-COVID Study Group (2022) CSF Biomarkers in COVID-19 Associated Encephalopathy and Encephalitis Predict Long-Term Outcome. Front. Immunol. 13:866153.
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Observational study: prospective longitudinal cohort