Evidence map›Paper›PMID 37072219›Full record

Trial reportNeurology2023

Longitudinal Changes in Cognitive Test Scores in Patients With Relapsing-Remitting Multiple Sclerosis: An Analysis of the DECIDE Dataset.

Nina Castrogiovanni, Jop Mostert, Pavle Repovic, James D Bowen, Bernard M J Uitdehaag, Eva M M Strijbis, Gary R Cutter, Marcus W Koch

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01064401 (Multicenter, Double-blind, Randomized, Parallel-group, Monotherapy, Active-control Study to Determine the Efficacy and Safety of Daclizumab High Yield Process), which is not on this map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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.

NCT01064401 phase3completednot on this map

Multicenter, Double-blind, Randomized, Parallel-group, Monotherapy, Active-control Study to Determine the Efficacy and Safety of Daclizumab High Yield Process (DAC HYP) Versus Avonex® (Interferon β 1a) in Patients With Relapsing-Remitting Multiple Sclerosis

TypeinterventionalSponsorBiogenRan2010 to 2014Enrolled1,841ConditionsRelapsing-Remitting Multiple SclerosisArmsBIIB019 (Daclizumab High Yield Process), Interferon beta-1a Placebo, Interferon beta-1a, Daclizumab High Yield Process Placebo
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Intranasal insulin for improving cognitive function in multiple sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Plateau of practice effects and noise with repeat SDMT testing in multiple sclerosis.Multiple sclerosis (Houndmills, Basingstoke, England) · 2025
    Article
  9. Article
  10. Article
  11. Cognitive impairment in multiple sclerosis: from phenomenology to neurobiological mechanisms.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Review
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  13. Article
  14. Article
  15. Review
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  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Nina CastrogiovanniFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Jop MostertFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Pavle RepovicFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.ORCID 0000-0001-7358-6872
James D BowenFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Bernard M J UitdehaagFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Eva M M StrijbisFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Gary R CutterFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada.
Marcus W KochFrom the Department of Clinical Neurosciences (N.C., M.W.K.), University of Calgary, Canada; Department of Neurology (J.M.), Rijnstate Hospital, Arnhem, The Netherlands; Multiple Sclerosis Center (P.R., J.D.B.), Swedish Neuroscience Institute, Seattle, WA; Department of Neurology (B.M.J.U., E.M.M.S.), MS Center Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands; Department of Biostatistics (G.R.C.), University of Alabama at Birmingham; Department of Community Health Sciences (M.W.K.), University of Calgary, Canada. mwkoch@ucalgary.ca.ORCID 0000-0002-1693-6829

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesCognitive impairment is a common and impactful symptom of relapsing-remitting multiple sclerosis (RRMS). Cognitive outcome measures are often used in cross-sectional studies, but their performance as longitudinal outcome measures in clinical trials is not widely researched. In this study, we used data from a large clinical trial to describe change on the Symbol Digit Modalities Test (SDMT) and the Paced Auditory Serial Addition Test (PASAT) over up to 144 weeks of follow-up.

methodsWe used the data set from DECIDE (clinicaltrials.gov identifier NCT01064401), a large randomized controlled RRMS trial to describe change on the SDMT and PASAT over 144 weeks of follow-up. We compared change on these cognitive outcomes with change on the timed 25-foot walk (T25FW), a well-established physical outcome measure. We investigated several definitions for clinically meaningful change: any change, 4-point change, 8-point change, and 20% change for the SDMT, any change, 4-point change, and 20% change for the PASAT, and 20% change for the T25FW.

resultsDECIDE included 1,814 trial participants. SDMT and PASAT scores steadily improved throughout follow-up: the SDMT from a mean 48.2 (SD, 16.1) points at baseline to 52.6 (SD 15.2) at 144 weeks and the PASAT from 47.0 (SD 11.3) at baseline to 50.0 (SD 10.8) at 144 weeks. This improvement in scores is most likely due to a practice effect. Throughout the trial, participants were more likely to experience improvement than worsening of their SDMT and PASAT performance, whereas the number of worsening events on the T25FW steadily increased. Changing the definition of clinically meaningful change for the SDMT and PASAT or using a 6-month confirmation changed the overall number of worsening or improvement events but did not affect the overall behavior of these measures. DISCUSSION: Our findings suggest that the SDMT and PASAT scores do not accurately reflect the steady cognitive decline that people with RRMS experience. Both outcomes show postbaseline increases in scores, which complicates the interpretation of these outcome measures in clinical trials. More research into the size of these changes is needed before recommending a general threshold for clinically meaningful longitudinal change.

Indexed as

Cognitive DysfunctionMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingCross-Sectional StudiesHumansNeuropsychological Tests

Identifiers

PMID37072219
PMCPMC10351309

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Registered trials

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.