Evidence map›Paper›PMID 40220155›Full record

Trial reportJournal of neurology2025

Measuring cognitive change in secondary progressive MS: an analysis of the ASCEND cognition substudy.

Victoria Leavitt, Jop Mostert, Jacynthe Comtois, Ester Moral, Luis Brieva, Pavle Repovic, James D Bowen, Bernard Uitdehaag, Eva Strijbis, Gary Cutter and 1 more

Abstract readRandomized Controlled TrialClinical Trial, Phase III
PubMed Publisher
In one paragraph

Trial report in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Victoria LeavittDepartment of Neurology, Columbia University Irving Medical Center, New York, USA. vl2337@cumc.columbia.edu.ORCID http://orcid.org/0000-0001-8937-6079
Jop MostertDepartment of Neurology, Rijnstate Hospital, Arnhem, The Netherlands.
Jacynthe ComtoisDepartment of Medicine, Neurology Service, Hôpital Cité-de-La-Santé de Laval, Laval, Canada.
Ester MoralDepartment of Neurology, Hospital Sant Joan Despí Moisès Broggi, Barcelona, Spain.
Luis BrievaNeuroimmunology Group, Department of Medicine, Department of Neurology, University of Lleida-IRBLleida, Hospital Universitari Arnau de Vilanova, Lleida, Spain.
Pavle RepovicMultiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, USA.
James D BowenMultiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, USA.
Bernard UitdehaagDepartment of Neurology, MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Eva StrijbisDepartment of Neurology, MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Gary CutterDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, USA.
Marcus W KochDepartment of Clinical Neurosciences, University of Calgary, Calgary, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCognitive impairment is common in multiple sclerosis (MS). Accurate measurement of cognitive change is essential for clinical trials.

methodsThe change in cognitive scores, clinical metrics of physical disability, and neuroradiological metrics was quantified in data from a phase-3 randomized controlled trial of natalizumab in secondary progressive MS (SPMS). The adults diagnosed with SPMS for ≥ 2 years and Expanded Disability Status Scale (EDSS) scores from 3 to 6.5 were randomized to receive natalizumab or placebo for 96 weeks. We evaluated change in Symbol Digit Modalities Test (SDMT), Paced Auditory Serial Addition Test (PASAT), Selective Reminding Test (SRT), Brief Visuospatial Memory Test (BVMT-R), two subjective cognitive measures, Beck Depression Inventory (BDI-FS), Timed 25-foot Walk Test, Nine Hole Peg Test, measures of brain volume, and T2 lesion volume.

resultsThe outcomes were evaluated at baseline, 48-, and 96-week follow-up. There were no significant differences in cognitive change between treatment arms. SDMT and PASAT scores improved over 96-weeks: mean SDMT scores by 4.5 points (SD 9.3), mean PASAT scores by 2.4 points (SD 9.4). Verbal and visuospatial memory test performance showed no consistent change. All MRI measures showed decreased brain volumes. NHPT scores worsened little and T25FW showed steadily worsening scores.

conclusionsImprovements in SDMT and PASAT performance were observed regardless of treatment arm. These findings are consistent with prior studies in MS. As it is unlikely that cognition improves over time in people with a chronic neurologic disease, these results support the need for cognitive outcomes that overcome practice and learning effects to accurately quantify change.

Indexed as

Cognitive DysfunctionImmunologic FactorsMultiple Sclerosis, Chronic ProgressiveAdultDouble-Blind MethodFemaleFollow-Up StudiesHumansMagnetic Resonance ImagingMaleMiddle AgedNatalizumabNeuropsychological TestsImmunologic FactorsNatalizumabClinical trialsCognitionMultiple sclerosisOutcome measures

Identifiers

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Registered trials

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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.