Clinically relevant increases in serum neurofilament light chain and glial fibrillary acidic protein in patients with Susac syndrome

Author:

Plantone Domenico1ORCID,Sabatelli Eleonora2,Locci Sara1,Marrodan Mariano3ORCID,Laakso Sini M.45,Mateen Farrah J.6ORCID,Feresiadou Amalia78,Buelens Tom9,Bianco Assunta2ORCID,Fiol Marcela P.3ORCID,Correale Jorge310ORCID,Tienari Pentti1112ORCID,Calabresi Paolo213,De Stefano Nicola1,Iorio Raffaele213ORCID

Affiliation:

1. Department of Medicine, Surgery and Neuroscience University of Siena Siena Italy

2. Neurology Unit Fondazione Policlinico Universitario ‘A.Gemelli’ IRCCS Rome Italy

3. Neurology Department Fleni Buenos Aires Argentina

4. Clinical Neurosciences, Neurology University of Helsinki and Helsinki University Hospital Helsinki Finland

5. Translational Immunology Research Program, Faculty of Medicine University of Helsinki Helsinki Finland

6. Department of Neurology Massachusetts General Hospital Boston Massachusetts USA

7. Department of Neurology Uppsala University Hospital Uppsala Sweden

8. Department of Medical Sciences, Section of Neurology Uppsala University Uppsala Sweden

9. Department of Ophthalmology CHU St Pierre and Brugmann Brussels Belgium

10. Institute of Biological Chemistry and Biophysics (IQUIFIB) CONICET University of Buenos Aires Buenos Aires Argentina

11. Department of Neurology, Neurocenter Helsinki University Hospital Helsinki Finland

12. Research Program of Translational Immunology, Faculty of Medicine University of Helsinki Helsinki Finland

13. Department of Neuroscience Università Cattolica del Sacro Cuore Rome Italy

Abstract

AbstractBackground and purposeSerum levels of neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) are promising neuro‐axonal damage and astrocytic activation biomarkers. Susac syndrome (SS) is an increasingly recognized neurological condition and biomarkers that can help assess and monitor disease evolution are highly needed for the adequate management of these patients. sNfL and sGFAP levels were evaluated in patients with SS and their clinical relevance in the relapse and remission phase of the disease was assessed.MethodsAs part of a multicentre study that enrolled patients diagnosed with SS from six international centres, sNfL and sGFAP levels were assessed in 22 SS patients (nine during a relapse and 13 in remission) and 59 age‐ and sex‐matched healthy controls using SimoaTM assay Neurology 2‐Plex B Kit.ResultsSerum NfL levels were higher than those of healthy controls (p < 0.001) in SS patients and in both subgroups of patients in relapse and in remission (p < 0.001 for both), with significantly higher levels in relapse than in remission (p = 0.008). sNfL levels showed a negative correlation with time from the last relapse (r = −0.663; p = 0.001). sGFAP levels were slightly higher in the whole group of patients than in healthy controls (p = 0.046) and were more pronounced in relapse than in remission (p = 0.013).ConclusionIn SS patients, both sNFL and sGFAP levels increased compared with healthy controls. Both biomarkers had higher levels during clinical relapse and much lower levels in remission. sNFL was shown to be time sensitive to clinical changes and can be useful to monitor neuro‐axonal damage in SS.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Toward a serum biomarker of disease activity in Susac syndrome;European Journal of Neurology;2023-07-24

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