TY - JOUR
T1 - Steps toward the implementation of neurofilaments in multiple sclerosis
T2 - patient profiles to be prioritized in clinical practice
AU - Centonze, Diego
AU - Di Sapio, Alessia
AU - Brescia Morra, Vincenzo
AU - Colombo, Elena
AU - Inglese, Matilde
AU - Paolicelli, Damiano
AU - Salvetti, Marco
AU - Furlan, Roberto
N1 - Publisher Copyright:
Copyright © 2025 Centonze, Di Sapio, Brescia Morra, Colombo, Inglese, Paolicelli, Salvetti and Furlan.
PY - 2025
Y1 - 2025
N2 - Multiple sclerosis (MS) is a chronic central nervous system disease characterized by neurodegeneration and inflammation. Neurofilament light chain (NfL), a protein released during axonal injury, has gained recognition as a potential biomarker for monitoring MS progression and treatment response. Evidence indicates that blood NfL (bNfL) offers a minimally invasive, cost-effective tool for tracking neuroaxonal damage. Regular bNfL assessments can identify subclinical disease activity, guide treatment intensification, and support individualized care. However, bNfL level evaluation is currently not optimized in Italian clinical practice. This work examines the utility of bNfL monitoring in clinical practice, focusing on optimizing its use within specific patient profiles, especially in resource-limited settings. bNfL testing, particularly in targeted MS patient profiles, including stable patients exhibiting subclinical signs of disease activity, such as fatigue, and patients off-treatment, represents a promising adjunct for personalized disease management. Its integration into clinical practice, alongside MRI and clinical assessments, can enhance decision-making and improve care efficiency, especially in settings with limited MRI resources. Further research is needed to standardize testing protocols and establish disease-specific cutoffs.
AB - Multiple sclerosis (MS) is a chronic central nervous system disease characterized by neurodegeneration and inflammation. Neurofilament light chain (NfL), a protein released during axonal injury, has gained recognition as a potential biomarker for monitoring MS progression and treatment response. Evidence indicates that blood NfL (bNfL) offers a minimally invasive, cost-effective tool for tracking neuroaxonal damage. Regular bNfL assessments can identify subclinical disease activity, guide treatment intensification, and support individualized care. However, bNfL level evaluation is currently not optimized in Italian clinical practice. This work examines the utility of bNfL monitoring in clinical practice, focusing on optimizing its use within specific patient profiles, especially in resource-limited settings. bNfL testing, particularly in targeted MS patient profiles, including stable patients exhibiting subclinical signs of disease activity, such as fatigue, and patients off-treatment, represents a promising adjunct for personalized disease management. Its integration into clinical practice, alongside MRI and clinical assessments, can enhance decision-making and improve care efficiency, especially in settings with limited MRI resources. Further research is needed to standardize testing protocols and establish disease-specific cutoffs.
KW - MS biomarker
KW - blood NfL
KW - clinical practice
KW - multiple sclerosis
KW - neurofilament light chain
UR - https://www.scopus.com/pages/publications/105002459945
U2 - 10.3389/fneur.2025.1571605
DO - 10.3389/fneur.2025.1571605
M3 - Article
AN - SCOPUS:105002459945
SN - 1664-2295
VL - 16
JO - Frontiers in Neurology
JF - Frontiers in Neurology
M1 - 1571605
ER -