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dc.creatorAloizou A.-M., Liampas I., Provatas A., Brotis A., Siokas V., Bakritzis C., Liakos P., Tsouris Z., Dardiotis E.en
dc.date.accessioned2023-01-31T07:31:01Z
dc.date.available2023-01-31T07:31:01Z
dc.date.issued2022
dc.identifier10.1016/j.msard.2022.103940
dc.identifier.issn22110348
dc.identifier.urihttp://hdl.handle.net/11615/70457
dc.description.abstractBackground: Multiple Sclerosis (MS) is the most common autoimmune disease of the central nervous system. Up to this day, no single accurate prognostic biomarker has been established in this disease. Neurofilaments are neuronal scaffold proteins released upon axonal damage and have gained attention as potential biomarkers in MS. Methods: Neurofilament light-chain (NfL) levels were measured in the cerebrospinal fluid (CSF) of 83 MS patients at their first hospital admission. The patients were longitudinally followed up and EDSS assessments (MS disability) were performed. MSSS scores (MS severity) were also calculated. For disability, patients were allocated to a benign (EDSS≤3) and non-benign course (EDSS>3), and for severity, to benign, moderate, and severe disease courses (benign: 0–1.999, moderate: 2–6.999, severe: 7–10). Results: NfL levels ranged between 185.8 and 24,440.0 ng/dl (median=995.8 ng/dl, mean=2032.9 ng/dl ±3107.8). The mean follow-up was 12.3 years (±6.7), ranging between 2 and 41 years (median=11 years). No significant association was found between NfL levels and age of onset (p = 0.858), disability (OR benign vs. non-benign: 0.916, p = 0.725), or severity (OR moderate vs. benign: 1.077, p = 0.791, OR severe vs. benign: 1.163, p = 0.642). A significant association was found between older age of onset and disability (OR benign vs. non-benign: 1.073, p = 0.005), and severity (OR moderate vs. benign: 1.063, p = 0.039, OR severe vs. benign: 1.122, p = 0.001). Conclusions: CSF NfL do not seem to be the ideal prognostic marker in MS. More research in this direction, with large follow-up periods, is needed to confirm our findings. © 2022en
dc.language.isoenen
dc.sourceMultiple Sclerosis and Related Disordersen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85131439403&doi=10.1016%2fj.msard.2022.103940&partnerID=40&md5=1d99a8721dffa8d3ddf0ddc1f1123a64
dc.subjectbiological markeren
dc.subjectaxonen
dc.subjectbiological markeren
dc.subjectadulten
dc.subjectArticleen
dc.subjectcerebrospinal fluiden
dc.subjectdisabilityen
dc.subjectdisease courseen
dc.subjectdisease durationen
dc.subjectdisease exacerbationen
dc.subjectdisease severityen
dc.subjectenzyme linked immunosorbent assayen
dc.subjectfemaleen
dc.subjectfollow upen
dc.subjecthospital admissionen
dc.subjecthumanen
dc.subjectlimit of quantitationen
dc.subjectlongitudinal studyen
dc.subjectlumbar punctureen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmultiple sclerosisen
dc.subjectneurofilamenten
dc.subjectprognostic assessmenten
dc.subjectcerebrospinal fluiden
dc.subjectintermediate filamenten
dc.subjectmultiple sclerosisen
dc.subjectprognosisen
dc.subjectAxonsen
dc.subjectBiomarkersen
dc.subjectHumansen
dc.subjectIntermediate Filamentsen
dc.subjectMultiple Sclerosisen
dc.subjectPrognosisen
dc.subjectElsevier B.V.en
dc.titleBaseline neurofilament levels in cerebrospinal fluid do not correlate with long-term prognosis in multiple sclerosisen
dc.typejournalArticleen


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