Related Experiment Video
Updated: Sep 9, 2025

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The Multiple Sclerosis Performance Test MSPT: An iPad-Based Disability Assessment Tool
Published on: June 30, 2014
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Persistent progression independent of relapse activity in multiple sclerosis
Chao Zhu1, Zhen Zhou2, Tomas Kalincik3,4
1Department of Neuroscience, School of Translational Medicine, Monash University, Melbourne, VIC 3004, Australia.
Brain Communications
|September 5, 2025
Summary
Disability progression in relapsing-remitting multiple sclerosis (RRMS) can reverse in one-third of patients. Younger age, lower baseline disability, and high-efficacy treatments predict this regression, reducing long-term disability risk.
Area of Science:
- Neurology
- Clinical Research
- Epidemiology
Background:
- Disability progression independent of relapse activity (PIRA) in relapsing-remitting multiple sclerosis (RRMS) can precede secondary progressive multiple sclerosis (SPMS).
- Understanding PIRA persistence is crucial for defining RRMS to SPMS transitions and informing treatment strategies.
- PIRA events may spontaneously regress, necessitating investigation into factors influencing persistence and non-persistence.
Purpose of the Study:
- To identify risk factors associated with the persistence and non-persistence of PIRA events in RRMS patients.
- To compare the long-term disability progression risks between patients with persistent and non-persistent PIRA.
- To examine the impact of baseline characteristics and treatment on PIRA regression.
Main Methods:
- A cohort study utilizing the MSBase registry (1995-2024) including 4713 RRMS patients with a PIRA event.
- Analysis of time to 6-month confirmed non-persistence of PIRA, time to Expanded Disability Status Scale (EDSS) 6, and time to SPMS.
- Propensity score matching was employed to compare outcomes between persistent and non-persistent PIRA groups, using stratified Cox regression models.
Main Results:
- Approximately one-third of RRMS patients experienced PIRA regression over a median follow-up of 8.7 years.
- Younger age, lower baseline EDSS, and use of high-efficacy disease-modifying therapies (DMTs) at baseline were associated with non-persistent PIRA (regression).
- Patients with non-persistent PIRA had significantly lower risks of reaching EDSS 6 (HR 0.19) and SPMS (HR 0.18) compared to those with persistent PIRA.
Conclusions:
- PIRA events can regress, with younger age, lower baseline disability, and high-efficacy DMT use predicting regression.
- Persistent PIRA is a significant risk factor for accelerated disability accumulation and progression to SPMS.
- These findings refine the understanding of PIRA dynamics and have implications for monitoring and managing RRMS patients.
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