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@ARTICLE{Konitsioti:1052352,
author = {Konitsioti, Agni M. and Schweitzer, Finja and Johannis,
Wibke and Steffen, Falk and Bittner, Stefan and Fink, Gereon
R. and Schroeter, Michael and Warnke, Clemens},
title = {{S}erum neurofilament light chain as a biomarker of disease
control in multiple sclerosis: a real-world cross-sectional
analysis of therapeutic regimens},
journal = {Journal of neurology},
volume = {273},
number = {1},
issn = {0367-004X},
address = {[Darmstadt]},
publisher = {Steinkopff},
reportid = {FZJ-2026-00954},
pages = {34},
year = {2026},
note = {Funding: Open Access funding enabled and organized by
Projekt DEAL. The study was supported by an unrestricted
grant from Novartis.},
abstract = {BackgroundSerum neurofilament light chain (sNfL) is an
established biomarker of disease activity and progression in
persons with multiple sclerosis (PwMS), with studies showing
elevated sNfL levels during relapses and positive
associations with disability scores.Objective To assess sNfL
levels in PwMS receiving different disease-modifying
therapies (DMTs), with a particular focus on
extended-interval dosing (EID) regimens in real-world
clinical practice.MethodsIn this two-center cross-sectional
study, 172 PwMS without relapses in the preceding three
months were included (University Hospital Cologne,
n = 125; University Hospital Mainz, n = 47).
Patients were categorized into the following groups: (1)
low-efficacy DMT (leDMT; n = 8), (2) natalizumab
standard-interval dosing (SID; every 4 weeks; n = 7),
(3) natalizumab EID (every 6–8 weeks; n = 53), (4)
ofatumumab (n = 17), (5) ocrelizumab SID (every 6
months; n = 48), (6) ocrelizumab EID (every 9 months;
n = 17), and (7) no DMT (n = 19). sNfL levels were
measured once in a cross-sectional design using an
electrochemiluminescence immunoassay.Results No significant
differences in sNfL levels were observed across DMT
subgroups in the ANCOVA analysis after adjusting for age and
the presence of new T2 lesions on the most recent cranial
MRI. However, PwMS receiving DMTs showed lower sNfL levels
compared with untreated patients. Notably EID of ocrelizumab
(every 9 months; 1.56 pg/mL, $95\%$ CI 1.26–1.85) and
natalizumab (every 8 weeks; 1.46 pg/mL, $95\%$ CI
1.29–1.64) was not associated with higher sNfL levels
compared to standard interval dosing (SID) of ocrelizumab
(1.45 pg/mL, $95\%$ CI 1.27–1.63) or natalizumab (1.13
pg/mL, $95\%$ CI 0.68–1.58).Conclusion EID regimens were
not associated with increased sNfL levels, suggesting that
they may effectively limit neuroaxonal damage. Larger
studies that assess the added value sNfL monitoring for
safely personalizing treatment intervals in PwMS with
initially active disease are needed.},
cin = {INM-3},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406},
pnm = {5251 - Multilevel Brain Organization and Variability
(POF4-525)},
pid = {G:(DE-HGF)POF4-5251},
typ = {PUB:(DE-HGF)16},
doi = {10.1007/s00415-025-13573-4},
url = {https://juser.fz-juelich.de/record/1052352},
}