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Relapses and disability accumulation in progressive multiple sclerosis

. 2015 Jan 06 ; 84 (1) : 81-8. [epub] 20141114

Language English Country United States Media print-electronic

Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't

Grant support
R01 GM092993 NIGMS NIH HHS - United States
R01 NS058698 NINDS NIH HHS - United States
R01 NS032129 NINDS NIH HHS - United States
R01 NS024180 NINDS NIH HHS - United States
R21 NS073684 NINDS NIH HHS - United States
CA 1060A11 NCI NIH HHS - United States
UL1 TR000135 NCATS NIH HHS - United States
R01 NS049577 NINDS NIH HHS - United States
2P50NS038667 NINDS NIH HHS - United States
R01 NS048357 NINDS NIH HHS - United States
NS065829 NINDS NIH HHS - United States
R01 NS060881 NINDS NIH HHS - United States
UL1RR024150 NCRR NIH HHS - United States

Links

PubMed 25398229
PubMed Central PMC4336097
DOI 10.1212/wnl.0000000000001094
PII: WNL.0000000000001094
Knihovny.cz E-resources

OBJECTIVE: 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.

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