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Published on: December 9, 2015
Disease-modifying therapy usage in patients with multiple sclerosis in France: A 6-year population-based study
S Leblanc1, J Roux1, H Tillaut1
1Univ Rennes, EHESP, REPERES (Pharmacoepidemiology and health services research) - EA 7449, 15, avenue du Professeur Léon Bernard, CS 74312, 35000 Rennes, France.
French health data reveals disease-modifying therapy (DMT) use in multiple sclerosis (MS) patients. Over half received DMTs, with usage decreasing with age and varying by comorbidities and healthcare access.
Area of Science:
- Neurology
- Public Health
- Pharmacovigilance
Background:
- Limited data on disease-modifying therapy (DMT) use in multiple sclerosis (MS) often stems from biased clinical series.
- French national health administrative data offers comprehensive MS population coverage and DMT prescription information.
Purpose of the Study:
- To characterize DMT usage patterns across the entire French MS patient population between 2010 and 2015.
- To analyze longitudinal therapeutic sequences and classify patients based on treatment patterns.
Main Methods:
- Utilized French national health data system (covering 97% of the population) to identify MS patients over six years.
- Employed state sequence analysis to longitudinally track patients initiating DMTs in 2010 and categorize them into distinct therapeutic pattern groups.
- Compared characteristics of treated versus untreated patients and analyzed healthcare service utilization.
Main Results:
- Identified 112,415 MS patients; 54.0% received at least one DMT. Treatment probability decreased with age.
- Four patient clusters emerged from state sequence analysis: primarily first-line DMT users (57.0%), second-line DMT users (13.1%), off-label users (7.3%), and minimally treated (22.6%).
- Treatment group classification correlated with age, disease duration, pregnancy, disability, care utilization, and mortality.
Conclusions:
- Exhaustive French national health data enabled a detailed, national-level description of MS DMT use.
- State sequence analysis successfully identified four homogeneous patient groups based on longitudinal treatment data.
- First-line treatments remain predominant, though specific agents may have evolved post-2015.
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