TY - JOUR
T1 - Corticosteroid treatment of multiple sclerosis relapses is associated with lower disability worsening over 5 years
AU - Roberts, Jodie I.
AU - Sharmin, Sifat
AU - Horakova, Dana
AU - Kubala Havrdova, Eva
AU - Ozakbas, Serkan
AU - Lugaresi, Alessandra
AU - Tomassini, Valentina
AU - Alroughani, Raed
AU - Buzzard, Katherine
AU - Skibina, Olga
AU - Boz, Cavit
AU - Turkoglu, Recai
AU - Maimone, Davide
AU - Yamout, Bassem
AU - Khoury, Samia Joseph
AU - Spitaleri, Daniele
AU - Lechner-Scott, Jeannette
AU - Girard, Marc
AU - Duquette, Pierre
AU - Al-Asmi, Abdullah
AU - Ampapa, Radek
AU - Foschi, Matteo
AU - Surcinelli, Andrea
AU - Patti, Francesco
AU - Van Pesch, Vincent
AU - Ramo-Tello, Cristina
AU - Sánchez-Menoyo, José Luis
AU - Altintas, Ayse
AU - Grammond, Pierre
AU - Cartechini, Elisabetta
AU - Csepany, Tunde
AU - Laureys, Guy
AU - Willekens, Barbara
AU - Roos, Izanne
AU - Kalincik, Tomas
AU - MSBase Study Group
AU - Grand'maison, Francois
AU - Cabrera-Gomez, Jose Antonio
AU - Roullet, Etienne
AU - Campbell, Jamie
AU - Zwanikken, Cees
AU - Braber-Moerland, Leontien Den
AU - Inshasi, Jihad
AU - Deri, Norma
AU - Firstenfeld, Alfredo
AU - Saladino, Maria Laura
AU - Cristiano, Edgardo
AU - Rojas, Juan Ingacio
AU - Vrech, Carlos
AU - Shaw, Cameron
AU - Shuey, Neil
AU - John, Nevin
AU - Hodgkinson, Suzanne
AU - Garber, Justin
AU - Slee, Mark
AU - Mccombe, Pamela
AU - Boggild, Mike
AU - Taylor, Bruce
AU - Walt, Anneke van der
AU - Butzkueven, Helmut
AU - Macdonell, Richard
AU - Hardy, Todd
AU - Vucic, Steve
AU - Mccombe, Pamela
AU - Decoo, Danny
AU - Wijmeersch, Bart Van
AU - Vasconcelos, Claudia
AU - Prevost, Julie
AU - Moore, Fraser
AU - Lapointe, Emmanuelle
AU - Oh, Jiwon
AU - Zakaria, Magd
AU - Shalaby, Nevin
AU - Olascoaga, Javier
AU - Oreja-Guevara, Celia
AU - Eichau, Sara
AU - Dominguez, Jose Andres
AU - Blanco, Yolanda
AU - Gray, Orla
AU - Grigoriadis, Nikolaos
AU - Piroska, Imre
AU - Simo, Magdolna
AU - Rajda, Cecilia
AU - Mcguigan, Chris
AU - Singhal, Bhim
AU - Khurana, Dheeraj
AU - Shaygannejad, Vahid
AU - Amato, Maria Pia
AU - Gregorio, Maria Di
AU - Solaro, Claudio
AU - Petkovska-Boskova, Tatjana
AU - Cauchi, Marija
AU - Gerlach, Oliver
AU - Hupperts, Raymond
AU - Gans, Koen de
AU - Verheul, Freek
AU - Sinnige, L. G.F.
AU - Mason, Deborah
AU - Schepel, Jan
AU - Alkhaboori, Jabir
AU - Sa, Maria Jose
AU - Mihaela, Simu
AU - Al-Harbi, Talal
AU - Gouider, Riadh
AU - Mrabet, Saloua
AU - Karabudak, Rana
AU - Marriott, Mark
AU - Kilpatrick, Trevor
AU - King, John
AU - Nguyen, Ai Lan
AU - Dwyer, Chris
AU - Monif, Mastura
AU - Taylor, Lisa
AU - Baker, Josephine
AU - Larochelle, Catherine
AU - Chisari, Clara
AU - D'amico, Emanuele
AU - Salvatore, Lo Fermo
AU - Diamanti, Matteo
AU - Sartori, Charlotte
AU - Farr, Pamela
AU - Moore, Rein
AU - Stupar, Dusko
AU - Tang, Cynthia
AU - Smirnova, Sonya
PY - 2025/12
Y1 - 2025/12
N2 - Background: Corticosteroid treatment of multiple sclerosis (MS) relapses is assumed to improve the speed of relapse recovery, without modifying long-term disability risk. We aimed to re-evaluate this assumption in a large cohort of individuals with MS. Methods: Individuals with clinically definite MS and ≥3 Expanded Disability Status Scale (EDSS) measurements over ≥12 months were identified within the international neuroimmunology registry MSBase. Individuals were required to have ≥1 relapse, with complete information on relapse treatment, phenotype and severity for all documented relapses. The primary outcome was disability worsening confirmed over 12 months. The association of the cumulative number of steroid-treated and untreated relapses (as a time-varying exposure) with disability worsening was evaluated with Cox proportional hazards. Results: In total, 3673 individuals met the inclusion criteria (71% female, mean age 38 years, mean disability EDSS step 2); 5809 relapses (4671 treated/1138 untreated) were captured (annualised relapse rate 0.19). Over the study period (total 30 175 person-years), 32.7% reached the outcome of confirmed disability worsening (median survival time 5.2 years). Non-treated relapses were associated with a higher risk of disability worsening (HR 1.72, 95% CI 1.57 to 1.88) than steroid-treated relapses (HR 1.50, 95% CI 1.43 to 1.57). This association was modified by the efficacy of disease-modifying therapy at the time of relapse. Conclusions: Our results suggest that a lack of steroid treatment of MS relapses is associated with a higher risk of future disability worsening. Hence, corticosteroid treatment of MS relapses may impact not only the speed of recovery but also the severity of residual structural damage.
AB - Background: Corticosteroid treatment of multiple sclerosis (MS) relapses is assumed to improve the speed of relapse recovery, without modifying long-term disability risk. We aimed to re-evaluate this assumption in a large cohort of individuals with MS. Methods: Individuals with clinically definite MS and ≥3 Expanded Disability Status Scale (EDSS) measurements over ≥12 months were identified within the international neuroimmunology registry MSBase. Individuals were required to have ≥1 relapse, with complete information on relapse treatment, phenotype and severity for all documented relapses. The primary outcome was disability worsening confirmed over 12 months. The association of the cumulative number of steroid-treated and untreated relapses (as a time-varying exposure) with disability worsening was evaluated with Cox proportional hazards. Results: In total, 3673 individuals met the inclusion criteria (71% female, mean age 38 years, mean disability EDSS step 2); 5809 relapses (4671 treated/1138 untreated) were captured (annualised relapse rate 0.19). Over the study period (total 30 175 person-years), 32.7% reached the outcome of confirmed disability worsening (median survival time 5.2 years). Non-treated relapses were associated with a higher risk of disability worsening (HR 1.72, 95% CI 1.57 to 1.88) than steroid-treated relapses (HR 1.50, 95% CI 1.43 to 1.57). This association was modified by the efficacy of disease-modifying therapy at the time of relapse. Conclusions: Our results suggest that a lack of steroid treatment of MS relapses is associated with a higher risk of future disability worsening. Hence, corticosteroid treatment of MS relapses may impact not only the speed of recovery but also the severity of residual structural damage.
KW - CLINICAL NEUROLOGY
KW - DEMYELINATING DISEASES
KW - EVIDENCE-BASED NEUROLOGY
KW - MULTIPLE SCLEROSIS
UR - https://www.scopus.com/pages/publications/105012431984
U2 - 10.1136/jnnp-2025-336343
DO - 10.1136/jnnp-2025-336343
M3 - Article
C2 - 40721309
AN - SCOPUS:105012431984
SN - 0022-3050
VL - 96
SP - 1185
EP - 1193
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 12
ER -