Relapses and disability accumulation in progressive multiple sclerosis
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
PubMed
25398229
PubMed Central
PMC4336097
DOI
10.1212/wnl.0000000000001094
PII: WNL.0000000000001094
Knihovny.cz E-resources
- MeSH
- Multiple Sclerosis, Chronic Progressive drug therapy physiopathology MeSH
- Adult MeSH
- Immunologic Factors therapeutic use MeSH
- Kaplan-Meier Estimate MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Multivariate Analysis MeSH
- Disability Evaluation MeSH
- Disease Progression MeSH
- Proportional Hazards Models MeSH
- Recurrence MeSH
- Severity of Illness Index MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Immunologic Factors MeSH
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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Poor early relapse recovery affects onset of progressive disease course in multiple sclerosis