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A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
Published on: December 9, 2015
Disability progression in relapse-free multiple sclerosis patients on fingolimod versus interferon-beta/glatiramer
Viktor von Wyl1, Pascal Benkert2, André Moser3
1Department of Epidemiology, Biostatistics and Prevention Institute, University of Zürich, Zürich, Switzerland/ Swiss Multiple Sclerosis Registry, Epidemiology, Biostatistics and Prevention Institute, University of Zürich, Zürich, Switzerland.
Background:
Disability progression independent of relapses (PIRA) has been described as a frequent phenomenon in relapsing-remitting multiple sclerosis (RRMS).
Objective:
To compare the occurrence of disability progression in relapse-free RRMS patients on interferon-beta/glatiramer acetate (IFN/GA) versus fingolimod.
Methods:
This study is based on data from the Swiss association for joint tasks of health insurers. Time to relapse and 12-month confirmed disability progression were compared between treatment groups using multivariable Cox regression analysis with confounder adjustment. Inverse-probability weighting was applied to correct for the bias that patients on fingolimod have a higher chance to remain relapse-free than patients on IFN/GA.
Results:
We included 1640 patients (64% IFN/GA, 36% fingolimod, median total follow-up time = 4-5 years). Disease-modifying treatment (DMT) groups were well balanced with regard to potential confounders. Disability progression was observed in 155 patients (8.8%) on IFN/GA and 51 (7.6%) on fingolimod, of which 44 and 23 were relapse-free during the initial DMT, respectively. Adjusted standard regression analysis on all patients indicated that those on fingolimod experience less frequently disability progression compared with IFN/GA (hazard ratio = 0.53 (95% confidence interval = 0.37-0.76)). After bias correction, this was also true for patients without relapses (hazard ratio=0.56 (95% confidence interval = 0.32-0.98).
Conclusion:
Our analysis indicates that fingolimod is superior to IFN/GA in preventing disability progression in both relapsing and relapse-free, young, newly diagnosed RRMS patients.
Insights
Fingolimod significantly reduces disability progression in relapsing-remitting multiple sclerosis (RRMS) compared to interferon-beta/glatiramer acetate (IFN/GA). This benefit was observed in both relapsing and relapse-free patients, highlighting fingolimod
Area of Science:
- Neurology
- Immunology
- Clinical Trials
Background:
- Disability progression independent of relapses (PIRA) is a frequent occurrence in relapsing-remitting multiple sclerosis (RRMS).
- Understanding factors influencing PIRA is crucial for optimizing treatment strategies in RRMS.
Purpose of the Study:
- To compare the incidence of disability progression in relapse-free RRMS patients treated with interferon-beta/glatiramer acetate (IFN/GA) versus fingolimod.
- To evaluate the efficacy of fingolimod in preventing disability progression, considering both relapsing and relapse-free disease courses.
Main Methods:
- Retrospective analysis of 1640 RRMS patients from Swiss health insurance data.
- Comparison of time to relapse and 12-month confirmed disability progression using multivariable Cox regression.
- Application of inverse-probability weighting to correct for biases in treatment group selection.
Main Results:
- Fingolimod use was associated with a significantly lower frequency of disability progression compared to IFN/GA (HR=0.53).
- This protective effect of fingolimod remained significant even after bias correction and in relapse-free patients (HR=0.56).
- Disability progression was observed in 8.8% of IFN/GA patients and 7.6% of fingolimod patients.
Conclusions:
- Fingolimod demonstrates superior efficacy over IFN/GA in preventing disability progression in young, newly diagnosed RRMS patients.
- The benefits of fingolimod extend to both relapsing and relapse-free disease states, suggesting a broad impact on disease course.
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