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Abstract Details

Early Treatment Can Postpone the Time to Disability Pension in Relapsing-Remitting Multiple Sclerosis
Multiple Sclerosis
P17 - Poster Session 17 (11:45 AM-12:45 PM)
12-002

To assess the association between early treatment and the risk of disability pension in patients with relapsing-remitting multiple sclerosis (RRMS). 

Early initiation of disease-modifying therapy (DMT) has shown beneficial effects on clinical outcomes in patients with RRMS, but the impact on socioeconomic outcomes remain unclear.

Using the nationwide Danish Multiple Sclerosis Registry, we included patients with an onset of RRMS from 1. January 1996 to 1. January 2016. After four years from onset, patients were categorized according to their first treatment start: Within 1 year of onset (early), between 1 and 4 years (intermediate) and from 4 to 8 years (late). Data on socioeconomic parameters were obtained by linkage to nationwide, population-based registries. We assessed the association between the timing of DMT start and the rate of disability pension using Cox regressions.

The cohort consisted of 5208 patients with 1922 early starters, 2126 intermediate starters and 1160 late starters. Age and sex were evenly distributed in all groups, mean age: 37 (SD: ±9) years and male-female ratio: 1:2. Mean EDSS at baseline differed slightly: Early: 1.5 (SD: ±1), Intermediate: 1.7 (SD: ±1) and Late: 1.9 (SD: ± 1). Baseline levels of education and cohabitation status were similar, but the share of patients receiving financial support differed: Early 34%, Intermediate 29% and Late 14%. Compared to early initiators, the rate of receiving disability pension was increased with increasing time from onset to start of DMT: Intermediate: HR 1.33 [95% CI: 1.09-1.63] and Late: HR 1.88 [95% CI: 1.48-2.39]. Further, the risk of receiving disability pension was associated with increasing EDSS, presence of chronic comorbidities and poor labor market affiliation.

Early treatment may postpone the time to disability pension. Our findings support guidelines with a focus on early treatment initiation and emphasizes the importance of early diagnosis.

Authors/Disclosures
Malthe F. Wandall-Holm, MD (Danish Multiple Sclerosis Registry, Department of Neurology, Copenhagen Universi)
PRESENTER
Mr. Wandall-Holm has nothing to disclose.
Mathias Buron Mathias Buron has nothing to disclose.
No disclosure on file
Finn Sellebjerg, MD (Copenhagen University Hospital Rigshospitalet) Dr. Sellebjerg has received personal compensation for serving as an employee of Danish Multiple Sclerosis Society. Dr. Sellebjerg has received personal compensation in the range of $10,000-$49,999 for serving as a Consultant for Novartis. Dr. Sellebjerg has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Sellebjerg has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Sellebjerg has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Roche. Dr. Sellebjerg has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi Genzyme. Dr. Sellebjerg has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Biogen. Dr. Sellebjerg has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Roche. Dr. Sellebjerg has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Novartis. Dr. Sellebjerg has received personal compensation in the range of $500-$4,999 for serving as an officer or member of the Board of Directors for Gangsted Foundation. Dr. Sellebjerg has received personal compensation in the range of $500-$4,999 for serving as an officer or member of the Board of Directors for Warwara Larsen Foundation. The institution of Dr. Sellebjerg has received research support from Biogen. The institution of Dr. Sellebjerg has received research support from Merck. The institution of Dr. Sellebjerg has received research support from Novartis. The institution of Dr. Sellebjerg has received research support from Sanofi Genzyme. Dr. Sellebjerg has received publishing royalties from a publication relating to health care.
Melinda Magyari, MD Dr. Magyari has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Roche. Dr. Magyari has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Merck. Dr. Magyari has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Magyari has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Merck. Dr. Magyari has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Novartis. Dr. Magyari has received personal compensation in the range of $10,000-$49,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sanofi. Dr. Magyari has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Alexion. Dr. Magyari has received personal compensation in the range of $0-$499 for serving on a Scientific Advisory or Data Safety Monitoring board for Bristol Myers Squibb. The institution of Dr. Magyari has received research support from The Danish MS Society. The institution of Dr. Magyari has received research support from Biogen. The institution of Dr. Magyari has received research support from Novartis. The institution of Dr. Magyari has received research support from Roche. The institution of Dr. Magyari has received research support from Merck. The institution of Dr. Magyari has received research support from Sanofi.