Evidence map›Paper›PMID 41920324›Full record

ArticleJournal of neurology2026

Long-term disability after initiation of platform versus high-efficacy disease-modifying therapy in relapsing-onset multiple sclerosis.

Jie Guo, Tomas Olsson, Eva Johansson, Lars Alfredsson, Anna Karin Hedström

Abstract read
In one paragraph

Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jie GuoDepartment of Nutrition and Health, China Agricultural University, Beijing, China.
Tomas OlssonDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Eva JohanssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Lars AlfredssonInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Anna Karin HedströmDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden. anna.hedstrom@ki.se.ORCID http://orcid.org/0000-0002-6612-4749

Funding

Forskningsrådet om Hälsa, Arbetsliv och Välfärd 2015-00195Forskningsrådet om Hälsa, Arbetsliv och Välfärd 2019-00697Swedish Brain Foundation FO2020-0077Swedish Brain Foundation FO2022-0123Swedish Brain Foundation FO2024-0344Vetenskapsrådet 2016-02349Vetenskapsrådet 2017-00777Vetenskapsrådet 2020-01998Vetenskapsrådet 2024-02565
6 · The paper itself

Abstract

backgroundSeveral observational studies have compared high-efficacy and platform disease-modifying therapies (DMTs) with respect to long-term disability in relapsing-onset multiple sclerosis (MS), yet it remains unclear whether observed differences reflect relapse-associated worsening (RAW), progression independent of relapse activity (PIRA), or both.

methodsWe included 2,563 DMT-naïve individuals with relapsing-onset MS enrolled in a population-based study linked to the Swedish MS registry (40 clinics, 2005-2019). The exposure was initial DMT efficacy class (platform versus high-efficacy therapy), with platform as the reference. Cox models estimated hazard ratios (HRs) with 95% confidence intervals (CIs) for RAW, PIRA, and time to EDSS 3 and 4. EDSS trajectories were modeled using mixed-effects models. Follow-up started at DMT initiation and was censored at treatment switch, discontinuation, death, drop-out, or study end.

resultsAt treatment initiation, 1,987 participants started a platform DMT and 576 a high-efficacy DMT. High-efficacy therapy was associated with a lower risk of RAW (HR 0.60, 95% CI 0.38-0.92), while the risk of PIRA did not differ between treatment groups (HR 1.05, 95% CI 0.79-1.39). Risks of reaching EDSS 3 and EDSS 4 were also lower with high-efficacy DMT (EDSS 3: HR 0.26, 95% CI 0.17-0.38; EDSS 4: HR 0.32, 95% CI 0.18-0.54). EDSS trajectories increased more steeply among platform-treated participants, with partial convergence toward the high-efficacy group over time.

conclusionsOur findings suggest that inflammatory and relapse-independent components of MS disability respond differently to current therapies and highlight the need for complementary neuroprotective strategies.

Indexed as

Immunologic FactorsMultiple Sclerosis, Relapsing-RemittingAdultDisability EvaluationDisease ProgressionFemaleFollow-Up StudiesHumansMaleMiddle AgedRegistriesSwedenTreatment OutcomeImmunologic FactorsDisease-modifying therapyExpanded disability status scaleMultiple sclerosisProgression independent of relapse activityRelapse-associated worsening

Identifiers

PMID41920324
PMCPMC13043616

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.