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Biomarkers of response to ocrelizumab in relapsing-remitting multiple sclerosis

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dc.contributor.author Rodríguez-Jorge, Fernando
dc.contributor.author Fernández-Velasco, José-Ignacio
dc.contributor.author Villarrubia, Noelia
dc.contributor.author Gracia-Gil, Julia
dc.contributor.author Fernández, Eva
dc.contributor.author Meca-Lallana, Virginia
dc.contributor.author Díaz-Pérez, Carolina
dc.contributor.author Sainz-de-la-Maza, Susana
dc.contributor.author Pacheco, Eva-María
dc.contributor.author Quiroga, Ana
dc.contributor.author Ramio-Torrenta, Lluis
dc.contributor.author Martínez-Yélamos, Sergio
dc.contributor.author Bau, Laura
dc.contributor.author Monreal, Enric
dc.contributor.author López-Real, Ana-M
dc.contributor.author Rodero-Romero, Alexander
dc.contributor.author Borrega, Laura
dc.contributor.author Díaz, Santiago
dc.contributor.author Eguia, Pablo
dc.contributor.author Espino, Mercedes
dc.contributor.author Chico-García, Juan-Luis
dc.contributor.author Barrero, Francisco-Javier
dc.contributor.author Martínez-Gines, María-Luisa
dc.contributor.author García-Domínguez, José-Manuel
dc.contributor.author de-la-Fuente, Soraya
dc.contributor.author Moreno, Irene
dc.contributor.author Sainz-Amo, Raquel
dc.contributor.author Mane-Martínez, MAlba
dc.contributor.author Caminero, Ana
dc.contributor.author Castellanos, Fernando
dc.contributor.author Gómez-López, Ana
dc.contributor.author Labiano-Fontcuberta, Andrés
dc.contributor.author Ayuso, Lucía
dc.contributor.author Abreu, Rossana
dc.contributor.author Hernández, Miguel-Ángel
dc.contributor.author Meca-Lallana, José-Eustasio
dc.contributor.author Martín-Aguilar, Lorena
dc.contributor.author Muriel-García, Alfonso
dc.contributor.author Masjuan, Jaime
dc.contributor.author Costa-Frossard, Lucienne
dc.contributor.author Villar, Luisa-María
dc.date.accessioned 2025-11-21T08:48:23Z
dc.date.available 2025-11-21T08:48:23Z
dc.date.issued 2024-11
dc.identifier.citation Rodríguez-Jorge F, Fernández-Velasco JI, Villarrubia N, Gracia-Gil J, Fernández E, Meca-Lallana V, et al. Biomarkers of response to ocrelizumab in relapsing-remitting multiple sclerosis. Front Immunol. 12 de noviembre de 2024;15:1480676.
dc.identifier.issn 1664-3224
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/22020
dc.description.abstract OBJECTIVE: To ascertain the changes of serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) values in relapsing-remitting multiple sclerosis (RRMS) patients treated with ocrelizumab and their association with treatment response. METHODS: Multicenter prospective study including 115 RRMS patients initiating ocrelizumab treatment between February 2020 and March 2022 followed during a year. Serum samples were collected at baseline and every 3 months to measure sNfL and sGFAP levels using single-molecule array (SIMOA) technology. Based on age and body mass index, sNfL values were standardized using z-score. NEDA (non-evidence of disease activity)-3 status was defined for patients free of disease activity after a year of follow-up. Inflammation (INFL) was considered when new relapses occurred during follow-up or new MRI lesions were found at 1-year exploration. PIRA (progression independent of relapse activity) was defined as disability progression occurring in the absence of relapses or new MRI activity. RESULTS: After a year on ocrelizumab, 85 patients (73.9%) achieved NEDA-3. Thirty patients did not achieve NEDA: 20 (17.4%) because of INFL and 10 (8.7%) because of PIRA. Of INFL patients, 6 (30.0%) had relapses, and 17 (85.0%) had at least one new MRI lesion at the 12-month examination. At baseline, INFL patients had higher sNfL (p = 0.0003) and sGFAP (p = 0.03) than the NEDA-3 group. PIRA patients mostly exhibited low sNfL and heterogeneous sGFAP levels. After a year, NEDA-3 and INFL patients showed similar decreases in sNfL (p < 0.0001) and sGFAP (p < 0.0001 for NEDA-3 and p = 0.001 for INFL ones). However, the decrease occurred earlier in NEDA-3 patients. Accordingly, sNfL > 1.5 z-score 3 months after ocrelizumab initiation indicated a higher risk of inflammation (OR = 13.6; p < 0.0001). Decrease in sGFAP values occurred later in both groups, with significant reductions observed at 12 months for INFL and 6 and 12 months for NEDA-3. No significant changes in sNfL or sGFAP were observed in PIRA patients. CONCLUSION: Ocrelizumab induced normalization of sNfL and sGFAP in the majority of NEDA-3 and inflammatory patients but did not cause changes in the PIRA group. Our data suggest that normalization of sNfL and sGFAP is associated with the lack of inflammatory-associated disease progression but it may not affect non-inflammatory PIRA.
dc.language.iso eng
dc.publisher FRONTIERS MEDIA SA
dc.rights Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/4.0/es/  *
dc.subject.mesh Humans
dc.subject.mesh Multiple Sclerosis, Relapsing-Remitting/drug therapy/blood
dc.subject.mesh Female
dc.subject.mesh Male
dc.subject.mesh Adult
dc.subject.mesh Antibodies, Monoclonal, Humanized/therapeutic use/adverse effects
dc.subject.mesh Biomarkers/blood
dc.subject.mesh Neurofilament Proteins/blood
dc.subject.mesh Prospective Studies
dc.subject.mesh Glial Fibrillary Acidic Protein/blood
dc.subject.mesh Middle Aged
dc.subject.mesh Immunologic Factors/therapeutic use
dc.subject.mesh Treatment Outcome
dc.subject.mesh Disease Progression
dc.title Biomarkers of response to ocrelizumab in relapsing-remitting multiple sclerosis
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 39606235
dc.relation.publisherversion https://www.frontiersin.org/articles/10.3389/fimmu.2024.1480676/full
dc.identifier.doi 10.3389/fimmu.2024.1480676
dc.journal.title Frontiers in Immunology


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Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional Excepto si se señala otra cosa, la licencia del ítem se describe como Atribución/Reconocimiento-NoComercial-SinDerivados 4.0 Internacional

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