P123 – Neurochemical signs of astrocytic and neuronal injury in acute COVID-19 normalizes during long-term follow-up

13. Övrigt

Nelly Kanberg1, Joel Simrén2, 3, Arvid Edén1, Lars-Magnus Andersson1, Staffan Nilsson4, Nicholas J Ashton3, Per-Daniel Sundvall5, Bengt Nellgård6, Kaj Blennow2, 3, Henrik Zetterberg2, 3, Magnus Gisslén1

1 Department of Infectious Diseases, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
2 Department of Psychiatry and Neurochemistry, Institute of Neuroscience & Physiology, The Sahlgrenska Academy at the University of Gothenburg, Mölndal, Sweden
3 Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden
4 Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
5 Research, Education, Development & Innovation, Primary Health Care, Region Västra Götaland, Sweden
6 Department of Anaesthesiology and Intensive care, Institution of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden

Bakgrund: Neurologic manifestations are well-recognized features of coronavirus disease 2019(COVID-19). However, the longitudinal association of biomarkers reflecting CNS impact and neurological symptoms is not known. We sought to determine whether plasma biomarkers of CNS injury were associated with neurologic sequelae after COVID-19.

Metod: Patients with confirmed acute COVID-19 were studied prospectively. Neurological symptoms were recorded during the acute phase of the disease and at six months follow-up, and blood samples were collected longitudinally. Healthy age-matched individuals were included as controls. We analysed plasma concentrations of neurofilament light-chain (NfL), glial fibrillary acidic protein (GFAp), and growth differentiation factor 15 (GDF-15).

Resultat: One hundred patients with mild (n=24), moderate (n=28), and severe (n=48) COVID-19 were followed for a median (IQR) of 225 (187–262) days.  In the acute phase, patients with severe COVID-19 had higher concentrations of NfL than all other groups (all p<0∙001), and higher GFAp than controls (p<0∙001). GFAp was also significantly increased in moderate disease (p<0∙05) compared with controls. NfL (r=0∙53, p<0∙001) and GFAp (r=0∙39, p<0∙001) correlated with GDF-15 during the acute phase. After six months, NfL and GFAp concentrations had normalized, with no persisting group differences. Despite this, 50 patients reported persistent neurological symptoms, most commonly fatigue (n=40), “brain-fog” (n=29), and changes in cognition (n=25). We found no correlation between persistent neurological symptoms and CNS injury biomarkers in the acute phase.

Slutsats: The normalization of CNS injury biomarkers in all individuals, regardless of previous disease severity or persisting neurological symptoms, indicates that post COVID-19 neurological sequelae are not accompanied by ongoing CNS injury.