Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/40471
Title: Disability accrual in primary and secondary progressive multiple sclerosis
Authors: Harding-Forrester, Sam
Roos, Izanne
Nguyen, Ai-Lan
Malpas, Charles B.
Diouf, Ibrahima
Moradi, Nahid
Sharmin , Sifat
Izquierdo, Guillermo
Eichau, Sara
Patti, Francesco
Horakova, Dana
Kubala Havrdova, Eva
Prat, Alexandre
Girard, Marc
Duquette, Pierre
Maison, Francois Grand
Onofrj, Marco
Lugaresi, Alessandra
Grammond, Pierre
Ozakbas, Serkan
Amato, Maria Pia
Gerlach, Oliver
Sola, Patrizia
Ferraro, Diana
Buzzard, Katherine
Skibina, Olga
Lechner-Scott, Jeannette
Alroughani, Raed
Boz, Cavit
Van Pesch, Vincent
Cartechini, Elisabetta
Terzi, Murat
Maimone, Davide
Ramo-Tello, Cristina
Yamout, Bassem
Khoury, Samia Joseph
La Spitaleri, Daniele
Sa, Maria Jose
Blanco, Yolanda
Granella, Franco
Slee, Mark
Butler, Ernest
Sidhom, Youssef
Gouider, Riadh
Bergamaschi, Roberto
Karabudak, Rana
Ampapa, Radek
Sanchez-Menoyo, Jose Luis
Prevost, Julie
Castillo-Trivino, Tamara
McCombe, Pamela A.
Macdonell, Richard
Laureys, Guy
Van Hijfte, Liesbeth
Oh, Jiwon
Altintas, Ayse
de Gans, Koen
Turkoglu, Recai
van der Walt, Anneke
Butzkueven, Helmut
Vucic, Steve
Barnett, Michael
Cristiano, Edgardo
Hodgkinson, Suzanne
Iuliano, Gerardo
Kappos, Ludwig
Kuhle, Jens
Shaygannejad, Vahid
Soysal, Aysun
Weinstock-Guttman, Bianca
VAN WIJMEERSCH, Bart 
Kalincik, Tomas
Issue Date: 2023
Publisher: BMJ PUBLISHING GROUP
Source: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 94 (9)
Abstract: BackgroundSome studies comparing primary and secondary progressive multiple sclerosis (PPMS, SPMS) report similar ages at onset of the progressive phase and similar rates of subsequent disability accrual. Others report later onset and/or faster accrual in SPMS. Comparisons have been complicated by regional cohort effects, phenotypic differences in sex ratio and management and variable diagnostic criteria for SPMS. MethodsWe compared disability accrual in PPMS and operationally diagnosed SPMS in the international, clinic-based MSBase cohort. Inclusion required PPMS or SPMS with onset at age >= 18 years since 1995. We estimated Andersen-Gill hazard ratios for disability accrual on the Expanded Disability Status Scale (EDSS), adjusted for sex, age, baseline disability, EDSS score frequency and drug therapies, with centre and patient as random effects. We also estimated ages at onset of the progressive phase (Kaplan-Meier) and at EDSS milestones (Turnbull). Analyses were replicated with physician-diagnosed SPMS. ResultsIncluded patients comprised 1872 with PPMS (47% men; 50% with activity) and 2575 with SPMS (32% men; 40% with activity). Relative to PPMS, SPMS had older age at onset of the progressive phase (median 46.7 years (95% CI 46.2-47.3) vs 43.9 (43.3-44.4); p<0.001), greater baseline disability, slower disability accrual (HR 0.86 (0.78-0.94); p<0.001) and similar age at wheelchair dependence. ConclusionsWe demonstrate later onset of the progressive phase and slower disability accrual in SPMS versus PPMS. This may balance greater baseline disability in SPMS, yielding convergent disability trajectories across phenotypes. The different rates of disability accrual should be considered before amalgamating PPMS and SPMS in clinical trials.
Notes: Kalincik, T (corresponding author), Univ Melbourne, Dept Med, CORe, Melbourne, Vic, Australia.
tomas.kalincik@unimelb.edu.au
Keywords: multiple sclerosis
Document URI: http://hdl.handle.net/1942/40471
ISSN: 0022-3050
e-ISSN: 1468-330X
DOI: 10.1136/jnnp-2022-330726
ISI #: 000989489100001
Rights: Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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