Evidence map›Paper›PMID 38751221›Full record

ArticleMultiple sclerosis (Houndmills, Basingstoke, England)2024

Improving explanation of motor disability with diffusion-based graph metrics at onset of the first demyelinating event.

Michael A Foster, Ferran Prados, Sara Collorone, Baris Kanber, Niamh Cawley, Indran Davagnanam, Marios C Yiannakas, Lola Ogunbowale, Ailbhe Burke, Frederik Barkhof and 4 more

Abstract read
In one paragraph

Article in Multiple sclerosis (Houndmills, Basingstoke, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Michael A FosterQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.ORCID 0000-0001-7201-7475
Ferran PradosQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Sara ColloroneQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.ORCID 0000-0003-1506-8983
Baris KanberQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Niamh CawleyQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Indran DavagnanamDepartment of Brain Repair & Rehabilitation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Marios C YiannakasQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Lola OgunbowaleStrabismus and Neuro-Ophthalmology Service, Moorfields Eye Hospital NHS Foundation Trust, London, UK.
Ailbhe BurkeStrabismus and Neuro-Ophthalmology Service, Moorfields Eye Hospital NHS Foundation Trust, London, UK.
Frederik BarkhofQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Claudia Am Gandini Wheeler-KingshottQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Olga CiccarelliQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Wallace BrownleeQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
Ahmed T ToosyQueen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.ORCID 0000-0002-4441-3750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConventional magnetic resonance imaging (MRI) does not account for all disability in multiple sclerosis.

objectiveThe objective was to assess the ability of graph metrics from diffusion-based structural connectomes to explain motor function beyond conventional MRI in early demyelinating clinically isolated syndrome (CIS).

methodsA total of 73 people with CIS underwent conventional MRI, diffusion-weighted imaging and clinical assessment within 3 months from onset. A total of 28 healthy controls underwent MRI. Structural connectomes were produced. Differences between patients and controls were explored; clinical associations were assessed in patients. Linear regression models were compared to establish relevance of graph metrics over conventional MRI.

resultsLocal efficiency (

conclusionGraph metrics are relevant early in demyelination. They show differences between patients and controls and have relationships with clinical outcomes. Segregation (local efficiency, clustering, transitivity) was particularly relevant. Combining graph metrics with conventional MRI better explained disability.

Indexed as

ConnectomeDemyelinating DiseasesAdultBrainDiffusion Magnetic Resonance ImagingDisability EvaluationFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedMultiple SclerosisYoung Adultclinically isolated CNS demyelinating syndromeconnectomediffusion MRIMRIMultiple sclerosis

Identifiers

PMID38751221
PMCPMC11134971

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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.