The Prognostic Significance of Early Blood Neurofilament Light Chain Concentration and Magnetic Resonance Imaging Variables in Relapse-onset Multiple Sclerosis
Overview
Authors
Affiliations
Background: Improved prognostication remains vital in multiple sclerosis to inform personalized treatment approaches. Blood neurofilament light (bNfL) is a promising prognostic biomarker, but to what extent it provides additional information, independent of established MRI metrics, is yet to be established.
Methods: We obtained all available bNfL data for 133 patients from a longitudinal observational cohort study. Patients were dichotomized into good or poor outcome groups based upon clinical and cognitive assessments performed 15 years after a clinically isolated syndrome. We performed longitudinal modeling of early NfL and MRI variables to examine differences between outcome groups.
Results: The bNfL dataset was incomplete, with one to three (mean 1.5) samples available per participant. Within 3 months of onset, bNfL was similar between groups. The bNfL concentration subsequently decreased in those with a good outcome, and remained persistently elevated in those with a poor outcome. By year 5, NfL in the poor outcome group was approximately double that of those with a good outcome (14.58 [10.40-18.77] vs. 7.71 [6.39-9.04] pg/ml, respectively). Differences were reduced after adjustment for longitudinal changes in T2LV, but trends persisted for a greater rate of increase in NfL in those with a poor outcome, independent of T2LV.
Conclusions: This analysis requires replication in cohorts with more complete bNfL datasets, but suggests that persistently elevated blood NfL may be more common in patients with a poor long-term outcome. Persistent elevation of blood NfL may provide additional prognostic information not wholly accounted for by standard monitoring techniques.
Ghezzi A, Neuteboom R Neurol Ther. 2023; 12(6):1867-1881.
PMID: 37682513 PMC: 10630260. DOI: 10.1007/s40120-023-00535-z.
Williams T, Heslegrave A, Zetterberg H, Miszkiel K, Barkhof F, Ciccarelli O Brain Behav. 2022; 12(9):e2700.
PMID: 35925940 PMC: 9480937. DOI: 10.1002/brb3.2700.