• Ingrid Anne Lie, Sezgi Kaçar, Kristin Wesnes, Iman Brouwer, Silje S Kvistad, Stig Wergeland, Trygve Holmøy, Rune Midgard, Alla Bru, Astrid Edland, Randi Eikeland, Sonia Gosal, Hanne F Harbo, Grethe Kleveland, Yvonne S Sørenes, Nina Øksendal, Kristin N Varhaug, Christian A Vedeler, Frederik Barkhof, Charlotte E Teunissen, Lars Bø, Øivind Torkildsen, Kjell-Morten Myhr, and Hugo Vrenken.
• Department of Clinical Medicine, University of Bergen, Bergen, Norway ingrid.lie@uib.no.
• J. Neurol. Neurosurg. Psychiatr. 2022 Jun 1; 93 (8): 849857849-57.

BackgroundThe predictive value of serum neurofilament light chain (sNfL) on long-term prognosis in multiple sclerosis (MS) is still unclear.ObjectiveInvestigate the relation between sNfL levels over a 2-year period in patients with relapsing-remitting MS, and clinical disability and grey matter (GM) atrophy after 10 years.Methods85 patients, originally enrolled in a multicentre, randomised trial of ω-3 fatty acids, participated in a 10-year follow-up visit. sNfL levels were measured by Simoa quarterly until month 12, and then at month 24. The appearance of new gadolinium-enhancing (Gd+) lesions was assessed monthly between baseline and month 9, and then at months 12 and 24. At the 10-year follow-up visit, brain atrophy measures were obtained using FreeSurfer.ResultsHigher mean sNfL levels during early periods of active inflammation (Gd+ lesions present or recently present) predicted lower total (β=-0.399, p=0.040) and deep (β=-0.556, p=0.010) GM volume, lower mean cortical thickness (β=-0.581, p=0.010) and higher T2 lesion count (β=0.498, p=0.018). Of the clinical outcomes, higher inflammatory sNfL levels were associated with higher disability measured by the dominant hand Nine-Hole Peg Test (β=0.593, p=0.004). Mean sNfL levels during periods of remission (no Gd+ lesions present or recently present) did not predict GM atrophy or disability progression.ConclusionHigher sNfL levels during periods of active inflammation predicted more GM atrophy and specific aspects of clinical disability 10 years later. The findings suggest that subsequent long-term GM atrophy is mainly due to neuroaxonal degradation within new lesions.© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

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