Neurological symptoms and axonal damage in COVID-19 survivors: are there sequelae?
The persistence of neurological symptoms after SARS-CoV-2 infection, as well as the presence of late axonal damage, is still unknown. We performed extensive systemic and neurological follow-up evaluations in 107 out of 193 consecutive patients admitted to the COVID-19 medical unit, University Hospit...
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| Veröffentlicht in: | Immunologic research Jg. 69; H. 6; S. 553 - 557 |
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| Hauptverfasser: | , , , , , , , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
New York
Springer US
01.12.2021
Springer Nature B.V |
| Schlagworte: | |
| ISSN: | 0257-277X, 1559-0755, 1559-0755 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | The persistence of neurological symptoms after SARS-CoV-2 infection, as well as the presence of late axonal damage, is still unknown. We performed extensive systemic and neurological follow-up evaluations in 107 out of 193 consecutive patients admitted to the COVID-19 medical unit, University Hospital of Verona, Italy between March and June 2020. We analysed serum neurofilament light chain (NfL) levels in all cases including a subgroup (
n
= 29) of patients with available onset samples. Comparisons between clinical and biomarker data were then performed. Neurological symptoms were still present in a significant number (
n
= 49) of patients over the follow-up. The most common reported symptoms were hyposmia (
n
= 11), fatigue (
n
= 28), myalgia (
n
= 14), and impaired memory (
n
= 11) and were more common in cases with severe acute COVID-19. Follow-up serum NfL values (15.2 pg/mL, range 2.4–62.4) were within normal range in all except 5 patients and did not differentiate patients with vs without persistent neurological symptoms. In patients with available onset and follow-up samples, a significant (
p
< 0.001) decrease of NfL levels was observed and was more evident in patients with a severe acute disease. Despite the common persistence of neurological symptoms, COVID-19 survivors do not show active axonal damage, which seems a peculiar feature of acute SARS-CoV-2 infection. |
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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| ISSN: | 0257-277X 1559-0755 1559-0755 |
| DOI: | 10.1007/s12026-021-09220-5 |