Relapses and disability accumulation in progressive multiple sclerosis

dc.contributor.authorSoldán, Mateo Paz
dc.contributor.authorNovotna, Martina
dc.contributor.authorAbou-Zeid, Nuhad E.
dc.contributor.authorKale, Nilüfer
dc.contributor.authorTutuncu, Melih
dc.contributor.authorCrusan, Daniel J.
dc.contributor.authorAtkinson, Elizabeth J.
dc.contributor.authorSiva, Aksel
dc.contributor.authorKeegan, Brian Mark
dc.contributor.authorPirko, Istvan
dc.contributor.authorPittock, Sean Joseph
dc.contributor.authorLucchinetti, Claudia Francesca
dc.contributor.authorWeinshenker, Brian G.
dc.contributor.authorRodriguez, Moses
dc.contributor.authorKantarci, Orhun H.
dc.contributor.departmentNeurology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:07:28Z
dc.date.available2025-01-24T12:07:28Z
dc.date.issued2015
dc.description.abstractObjective: We examined the effect of relapses-before and after progression onset-on the rate of postprogression disability accrual in a progressive multiple sclerosis (MS) cohort. Methods: We studied patients with primary progressive MS (n = 322) and bout-onset progressive MS (BOPMS) including single-attack progressive MS (n = 112) and secondary progressive MS (n = 421). The effect of relapses on time to Expanded Disability Status Scale (EDSS) score of 6 was studied using multivariate Cox regression analysis (sex, age at progression, and immunomodulation modeled as covariates). Kaplan-Meier analysis was performed using EDSS 6 as endpoint. Results: Preprogression relapses (hazard ratio [HR]: 1.63; 95% confidence interval [CI]: 1.34- 1.98), postprogression relapses (HR: 1.37; 95% CI: 1.11-1.70), female sex (HR: 1.19; 95% CI: 1.00-1.43), and progression onset after age 50 years (HR: 1.47; 95% CI: 1.21-1.78) were associated with shorter time to EDSS 6. Postprogression relapses occurred in 29.5% of secondary progressive MS, 10.7% of single-attack progressive MS, and 3.1% of primary progressive MS. Most occurred within 5 years (91.6%) after progressive disease onset and/or before age 55 (95.2%). Immunomodulation after onset of progressive disease course (HR: 0.64; 95% CI: 0.52-0.78) seemingly lengthened time to EDSS 6 (for BOPMS with ongoing relapses) when analyzed as a dichotomous variable, but not as a time-dependent variable. Conclusions: Pre- and postprogression relapses accelerate time to severe disability in progressive MS. Continuing immunomodulation for 5 years after the onset of progressive disease or until 55 years of age may be reasonable to consider in patients with BOPMS who have ongoing relapses. © 2014 American Academy of Neurology.
dc.identifier.doihttps://doi.org/10.1212/WNL.0000000000001094
dc.identifier.eid2-s2.0-84925936255
dc.identifier.pmid25398229
dc.identifier.urihttp://hdl.handle.net/10938/31524
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofNeurology
dc.sourceScopus
dc.subjectAdult
dc.subjectDisability evaluation
dc.subjectDisease progression
dc.subjectFemale
dc.subjectHumans
dc.subjectImmunologic factors
dc.subjectKaplan-meier estimate
dc.subjectMale
dc.subjectMiddle aged
dc.subjectMultiple sclerosis, chronic progressive
dc.subjectMultivariate analysis
dc.subjectProportional hazards models
dc.subjectRecurrence
dc.subjectSeverity of illness index
dc.subjectTreatment outcome
dc.subjectYoung adult
dc.subjectImmunologic factor
dc.subjectArticle
dc.subjectBout onset progressive multiple sclerosis
dc.subjectControlled study
dc.subjectDisability
dc.subjectDisease assessment
dc.subjectExpanded disability status scale
dc.subjectHuman
dc.subjectImmunomodulation
dc.subjectMajor clinical study
dc.subjectMultiple sclerosis
dc.subjectOnset age
dc.subjectPriority journal
dc.subjectRelapse
dc.subjectSex difference
dc.subjectSingle attack progressive multiple sclerosis
dc.subjectDisease course
dc.subjectKaplan meier method
dc.subjectPathophysiology
dc.subjectProportional hazards model
dc.subjectRecurrent disease
dc.titleRelapses and disability accumulation in progressive multiple sclerosis
dc.typeArticle

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