Effect of Natalizumab on sNfL and sGFAP Levels in Multiple Sclerosis Patients

Natalizumab is a highly effective therapy for multiple sclerosis (MS). The aim of this study was to evaluate serum neurofilament light chain (sNfL) and serum glial fibrillary acidic protein (sGFAP) in patients with relapsing-remitting MS treated with Natalizumab. sNfL and sGFAP were analyzed at baseline, 6 and 12 months post treatment using the single-molecule array (SiMoA) technique. We recruited matched healthy controls for comparison. The study included 54 patients, with a median age of 33 years (Interquartile range (IQR), 29-41), with 32 women (60%) and 76 healthy controls. A decrease in sNfL was observed at 6 (67%, <i>p</i> = 0.005) and 12 (72%, <i>p</i> < 0.0001) months compared to baseline. After two years, six patients experienced evidence of disease activity (EDA-3). The remaining ones had no evidence of disease activity (NEDA-3). NEDA-3 presented a remarkable reduction in sNfL (<i>p</i> < 0.0001) and sGFAP (<i>p</i> = 0.01) after 6 months of treatment that continued to be observed after 12 months compared to baseline. EDA-3 only reached a significant decrease in sNfL after 12 months; there were no significant changes in sGFAP values. Natalizumab leads to a decrease in sNfL, which is higher and occurs earlier in NEDA-3 patients. Patients also showed a significant reduction in sGFAP levels, which was not observed in the EDA-3 group.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2024-12-07
DOI
https://doi.org/10.3390/ijms252313153
Citations
4
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
1.70

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article

Effect of Natalizumab on sNfL and sGFAP Levels in Multiple Sclerosis Patients

Jaime Masjuán, Juan Luis Chico‐García, Enric Monreal, José Ignacio Fernández-Velasco et al.
4 citations
International Journal of Molecular Sciences
Multiple Sclerosis Research Studies
1.70
article

Effect of Natalizumab on sNfL and sGFAP Levels in Multiple Sclerosis Patients

Jaime Masjuán, Juan Luis Chico‐García, Enric Monreal, José Ignacio Fernández-Velasco, Alexander Rodero-Romero, Noelia Villarrubia, Fernando Rodríguez‐Jorge, Lucienne Costa‐Frossard, Raquel Sainz-Amo, Luisa María Villar, Susana Sainz de la Maza, José Luís Veiga-González
article en
4 citations

Abstract

Natalizumab is a highly effective therapy for multiple sclerosis (MS). The aim of this study was to evaluate serum neurofilament light chain (sNfL) and serum glial fibrillary acidic protein (sGFAP) in patients with relapsing-remitting MS treated with Natalizumab. sNfL and sGFAP were analyzed at baseline, 6 and 12 months post treatment using the single-molecule array (SiMoA) technique. We recruited matched healthy controls for comparison. The study included 54 patients, with a median age of 33 years (Interquartile range (IQR), 29-41), with 32 women (60%) and 76 healthy controls. A decrease in sNfL was observed at 6 (67%, <i>p</i> = 0.005) and 12 (72%, <i>p</i> < 0.0001) months compared to baseline. After two years, six patients experienced evidence of disease activity (EDA-3). The remaining ones had no evidence of disease activity (NEDA-3). NEDA-3 presented a remarkable reduction in sNfL (<i>p</i> < 0.0001) and sGFAP (<i>p</i> = 0.01) after 6 months of treatment that continued to be observed after 12 months compared to baseline. EDA-3 only reached a significant decrease in sNfL after 12 months; there were no significant changes in sGFAP values. Natalizumab leads to a decrease in sNfL, which is higher and occurs earlier in NEDA-3 patients. Patients also showed a significant reduction in sGFAP levels, which was not observed in the EDA-3 group.

International Journal of Molecular SciencesVol. 25(23)
Instituto de Salud Carlos III (ES), Spanish Multiple Sclerosis Network (ES), Instituto Ramón y Cajal de Investigación Sanitaria (ES), Hospital Universitario Ramón y Cajal (ES)
European Commission, Instituto de Salud Carlos III
Good health and well-being
Openalex Percentile: Top 15%
Multiple Sclerosis Research Studies
1.70
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