Progression independent of relapsing biology in multiple sclerosis: a real-word study

Progression independent of relapse activity (PIRA) implies disability progression in people with relapsing-remitting multiple sclerosis (RRMS) secondary to neurodegeneration. Mechanistically and biologically PIRA could impact the traditional distinction between progressive and relapsing-MS. Herein, we estimated progression independent of relapsing biology (PIRB) in a cohort of 823 participants with clinically-isolated syndrome/RRMS in Calgary, Canada using a modified criterion [excluding relapses, inflammatory MRI activity, interim disability worsening/improvement over the observation period, and progression secondary to alternative causes including formal conversion to secondary-progressive MS]. PIRB was rare and rates remained consistent across disease-modifying therapies (3.75% dimethyl fumarate, 3.67% fingolimod, 3.72% ocrelizumab, 3.52% minocycline) despite varied rates of disability progression. PIRB may offer a practical alternative to the concept of PIRA.

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Publication Details

Journal
Frontiers in Neurology
Published
2025-05-29
DOI
https://doi.org/10.3389/fneur.2025.1595929
Citations
2
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
2.94
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article

Progression independent of relapsing biology in multiple sclerosis: a real-word study

Carlos R. Cámara-Lemarroy, Heather Yong
2 citations
Frontiers in Neurology
Multiple Sclerosis Research Studies
2.94
article

Progression independent of relapsing biology in multiple sclerosis: a real-word study

Carlos R. Cámara-Lemarroy, Heather Yong
article en
2 citations

Abstract

Progression independent of relapse activity (PIRA) implies disability progression in people with relapsing-remitting multiple sclerosis (RRMS) secondary to neurodegeneration. Mechanistically and biologically PIRA could impact the traditional distinction between progressive and relapsing-MS. Herein, we estimated progression independent of relapsing biology (PIRB) in a cohort of 823 participants with clinically-isolated syndrome/RRMS in Calgary, Canada using a modified criterion [excluding relapses, inflammatory MRI activity, interim disability worsening/improvement over the observation period, and progression secondary to alternative causes including formal conversion to secondary-progressive MS]. PIRB was rare and rates remained consistent across disease-modifying therapies (3.75% dimethyl fumarate, 3.67% fingolimod, 3.72% ocrelizumab, 3.52% minocycline) despite varied rates of disability progression. PIRB may offer a practical alternative to the concept of PIRA.

Frontiers in NeurologyVol. 16
University of Calgary (CA)
Openalex Percentile: Top 10%
Multiple Sclerosis Research Studies
2.94
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