Disability accrual in primary and secondary progressive multiple sclerosis

Author:

Harding-Forrester SamORCID,Roos IzanneORCID,Nguyen Ai-Lan,Malpas Charles BORCID,Diouf Ibrahima,Moradi Nahid,Sharmin SifatORCID,Izquierdo Guillermo,Eichau SaraORCID,Patti Francesco,Horakova Dana,Kubala Havrdova Eva,Prat Alexandre,Girard Marc,Duquette Pierre,Grand'Maison Francois,Onofrj MarcoORCID,Lugaresi Alessandra,Grammond Pierre,Ozakbas, Serkan,Amato Maria Pia,Gerlach Oliver,Sola Patrizia,Ferraro DianaORCID,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 JosephORCID,La Spitaleri Daniele,Sa Maria Jose,Blanco Yolanda,Granella Franco,Slee Mark,Butler Ernest,Sidhom Youssef,Gouider RiadhORCID,Bergamaschi Roberto,Karabudak Rana,Ampapa Radek,Sánchez-Menoyo José Luis,Prevost Julie,Castillo-Trivino TamaraORCID,McCombe Pamela AORCID,Macdonell Richard,Laureys Guy,Van Hijfte Liesbeth,Oh Jiwon,Altintas Ayse,de Gans Koen,Turkoglu Recai,van der Walt AnnekeORCID,Butzkueven Helmut,Vucic SteveORCID,Barnett Michael,Cristiano Edgardo,Hodgkinson Suzanne,Iuliano Gerardo,Kappos LudwigORCID,Kuhle Jens,Shaygannejad Vahid,Soysal Aysun,Weinstock-Guttman Bianca,Van Wijmeersch Bart,Kalincik TomasORCID

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.

Funder

National Health and Medical Research Council of Australia

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

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