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Changes in the Risk of Reaching Multiple Sclerosis Disability Milestones In Recent Decades: A Nationwide Population-Based Cohort Study in Sweden

Overview
Journal JAMA Neurol
Date 2019 Mar 19
PMID 30882868
Citations 28
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Abstract

Importance: Clinicians' experience and findings from recent natural history studies suggest that multiple sclerosis (MS) may now be running a more slowly progressing course than before.

Objective: To investigate whether the risk of reaching MS disability milestones has changed over the last decade in Sweden.

Design, Setting, And Participants: A nationwide population-based retrospective cohort study. By April 2017, 12 512 patients with available information on demographics, MS phenotype, and date of MS onset and diagnosis were registered in the Swedish MS Registry of which 7331 patients with at least 2 recorded Expanded Disability Status Scale scores (EDSS) and diagnosed between January 1995 and December 2010 were included. No further exclusion criteria were applied. Patients were followed up until December 2016 with a median duration follow-up of 8.5 (interquartile range, 4.7-13.8) years. Statistical analysis began in April 2017.

Main Outcomes And Measures: Patients were followed up from MS onset date to the date of sustained EDSS 3.0, 4.0, and 6.0. To handle interval-censored observations, a Weibull model was fit, and the change in the risk of EDSS 3.0, 4.0, and 6.0 over calendar years was estimated and hazard ratios (HRs) with corresponding CIs were calculated.

Results: Of 7331 patients, 5196 (70.9%) were women, and the mean (SD) age at diagnosis was 38.3 (11.7) years. Adjusting for sex, number of clinic visits, diagnostic delay, and onset age, a 3% decrease per calendar year of diagnosis for the risk of sustained EDSS 3.0 (HR, 0.97; 95% CI, 0.96-0.97), a 6% decrease for the risk of EDSS 4.0 (HR, 0.94; 95% CI, 0.93-0.95), and a 7% decrease for the risk of EDSS 6.0 (HR, 0.93; 95% CI, 0.91-0.94) among patients with relapsing-onset MS was found. The trends were not significant for patients with progressive-onset MS (EDSS 3.0: HR, 1.01; 95% CI, 0.98-1.03; EDSS 4.0: HR, 1.00; 95% CI, 0.98-1.02; EDSS 6.0: HR, 1.00; 95% CI, 0.98-1.02).

Conclusions And Relevance: Risk of reaching major disability milestones has significantly decreased over the last decade in patients with relapsing-onset MS in Sweden. Several factors could potentially be responsible for this observation. However, given that no change was seen in disability accrual of patients with progressive-onset MS and the absence of efficacious treatment option in this group, increased use of more efficacious disease-modifying treatments could be a possible driver of this change.

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References
1.
Freilich J, Manouchehrinia A, Trusheim M, Baird L, Desbiens S, Berndt E . Characterization of annual disease progression of multiple sclerosis patients: A population-based study. Mult Scler. 2017; 24(6):786-794. DOI: 10.1177/1352458517706252. View

2.
Ontaneda D, Cohen J . EDSS improvement: recovery of function or noise?. Mult Scler. 2012; 18(11):1520-1. DOI: 10.1177/1352458512441689. View

3.
Kragt J, Nielsen J, van der Linden F, Polman C, Uitdehaag B . Disease progression in multiple sclerosis: combining physicians' and patients' perspectives?. Mult Scler. 2010; 17(2):234-40. DOI: 10.1177/1352458510385505. View

4.
Burkill S, Montgomery S, Hajiebrahimi M, Hillert J, Olsson T, Bahmanyar S . Mortality trends for multiple sclerosis patients in Sweden from 1968 to 2012. Neurology. 2017; 89(6):555-562. DOI: 10.1212/WNL.0000000000004216. View

5.
Kister I, Chamot E, Cutter G, Bacon T, Jokubaitis V, Hughes S . Increasing age at disability milestones among MS patients in the MSBase Registry. J Neurol Sci. 2012; 318(1-2):94-9. DOI: 10.1016/j.jns.2012.03.017. View