Ageing and remyelination failure in people with multiple sclerosis

One of the most promising strategies to delay, prevent, or reverse disability progression in multiple sclerosis is enhancing endogenous remyelination. While preclinical research has established a strong connection between ageing and remyelination failure, evidence for this same link in people with multiple sclerosis remains less secure. As clinical trials for remyelinating therapies progress, clarifying this relationship is essential. A deeper understanding could guide the selection of therapeutic candidates, refine patient selection, and optimize the timing of treatment delivery. In this review, we describe the available evidence that has investigated the impact of age on remyelination in people with multiple sclerosis. We categorize these into pathological, imaging and clinical studies. We explore the challenges in measuring remyelination in humans and determine the implications for the connection between remyelination and age. Current evidence suggests that there is reduced capacity for remyelination with advancing age in people with multiple sclerosis. However, these findings are at times inconsistent, and the precise contribution of ageing to remyelination failure is unclear. There does not appear to be an age cut-off beyond which remyelination is not possible, as there are pathological data supporting remyelination occurring, to some extent, across all ages. Interestingly, the impact of age may vary by lesion location. Further targeted research, specifically exploring the relationship between ageing and remyelination, is needed. With emerging evidence that ageing processes might be malleable, we conclude that targeting the biology of ageing might also be an important strategy to therapeutically enhance remyelination.

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Publication Details

Journal
Brain
Published
2025-10-02
DOI
https://doi.org/10.1093/brain/awaf373
Citations
1
Primary Topic
Multiple Sclerosis Research Studies
Type
article
Field-Weighted Citation Impact
1.47

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article

Ageing and remyelination failure in people with multiple sclerosis

J William L Brown, Robin J.M. Franklin, Nick Cunniffe, Alasdair Coles et al.
1 citations
Brain
Multiple Sclerosis Research Studies
1.47
article

Ageing and remyelination failure in people with multiple sclerosis

J William L Brown, Robin J.M. Franklin, Nick Cunniffe, Alasdair Coles, Trisha Mukherjee, Gioia Riboni-Verri, Christopher E McMurran, Jonathon Holland, Cyrus Daruwalla
article en
1 citations

Abstract

One of the most promising strategies to delay, prevent, or reverse disability progression in multiple sclerosis is enhancing endogenous remyelination. While preclinical research has established a strong connection between ageing and remyelination failure, evidence for this same link in people with multiple sclerosis remains less secure. As clinical trials for remyelinating therapies progress, clarifying this relationship is essential. A deeper understanding could guide the selection of therapeutic candidates, refine patient selection, and optimize the timing of treatment delivery. In this review, we describe the available evidence that has investigated the impact of age on remyelination in people with multiple sclerosis. We categorize these into pathological, imaging and clinical studies. We explore the challenges in measuring remyelination in humans and determine the implications for the connection between remyelination and age. Current evidence suggests that there is reduced capacity for remyelination with advancing age in people with multiple sclerosis. However, these findings are at times inconsistent, and the precise contribution of ageing to remyelination failure is unclear. There does not appear to be an age cut-off beyond which remyelination is not possible, as there are pathological data supporting remyelination occurring, to some extent, across all ages. Interestingly, the impact of age may vary by lesion location. Further targeted research, specifically exploring the relationship between ageing and remyelination, is needed. With emerging evidence that ageing processes might be malleable, we conclude that targeting the biology of ageing might also be an important strategy to therapeutically enhance remyelination.

BrainVol. 149(1)
University of Cambridge (GB), Granta Design (United Kingdom) (GB)
Action Medical Research, National Institute for Health and Care Research, Guarantors of Brain, Cambridge Trust, Patrick Berthoud Charitable Trust, Medical Research Council, NIHR Cambridge Biomedical Research Centre
Openalex Percentile: Top 15%
Multiple Sclerosis Research Studies
1.47
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