Evidence map›Paper›PMID 26991559›Full record

ArticleHuman brain mapping2016

The effect of inflammation and its reduction on brain plasticity in multiple sclerosis: MRI evidence.

Valentina Tomassini, Alessandro d'Ambrosio, Nikolaos Petsas, Richard G Wise, Emilia Sbardella, Marek Allen, Francesca Tona, Fulvia Fanelli, Catherine Foster, Marco Carnì and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Human brain mapping, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
3.7field-weighted citation impact, top 7% of its field
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 32 citations in OpenAlex.

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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

13 authors at 4 institutions in 3 countries.

Valentina TomassiniInstitute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, United Kingdom.
Alessandro d'AmbrosioInstitute of Psychological Medicine and Clinical Neurosciences, Cardiff University School of Medicine, United Kingdom.
Nikolaos PetsasDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Richard G WiseCardiff University Brain Research Imaging Centre (CUBRIC), Cardiff University School of Psychology, United Kingdom.
Emilia SbardellaDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Marek AllenCardiff University Brain Research Imaging Centre (CUBRIC), Cardiff University School of Psychology, United Kingdom.
Francesca TonaDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Fulvia FanelliDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Catherine FosterCardiff University Brain Research Imaging Centre (CUBRIC), Cardiff University School of Psychology, United Kingdom.
Marco CarnìDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Antonio GalloDepartment of Medical, Surgical, Neurological, Metabolic and Aging Sciences, Second University of Naples, Italy.
Patrizia PantanoDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Carlo PozzilliDepartment of Neurology and Psychiatry, Sapienza University of Rome, Italy.
Sapienza University of Rome · ITCardiff University · GBUniversity of Naples Federico II · ITFondazione Santa Lucia · IT

Funding

Medical Research Council MR/L010305/1
6 · The paper itself

Abstract

Brain plasticity is the basis for systems-level functional reorganization that promotes recovery in multiple sclerosis (MS). As inflammation interferes with plasticity, its pharmacological modulation may restore plasticity by promoting desired patterns of functional reorganization. Here, we tested the hypothesis that brain plasticity probed by a visuomotor adaptation task is impaired with MS inflammation and that pharmacological reduction of inflammation facilitates its restoration. MS patients were assessed twice before (sessions 1 and 2) and once after (session 3) the beginning of Interferon beta (IFN beta), using behavioural and structural MRI measures. During each session, 2 functional MRI runs of a visuomotor task, separated by 25-minutes of task practice, were performed. Within-session between-run change in task-related functional signal was our imaging marker of plasticity. During session 1, patients were compared with healthy controls. Comparison of patients' sessions 2 and 3 tested the effect of reduced inflammation on our imaging marker of plasticity. The proportion of patients with gadolinium-enhancing lesions reduced significantly during IFN beta. In session 1, patients demonstrated a greater between-run difference in functional MRI activity of secondary visual areas and cerebellum than controls. This abnormally large practice-induced signal change in visual areas, and in functionally connected posterior parietal and motor cortices, was reduced in patients in session 3 compared with 2. Our results suggest that MS inflammation alters short-term plasticity underlying motor practice. Reduction of inflammation with IFN beta is associated with a restoration of this plasticity, suggesting that modulation of inflammation may enhance recovery-oriented strategies that rely on patients' brain plasticity. Hum Brain Mapp 37:2431-2445, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

Adaptation, PhysiologicalAdaptation, PsychologicalAdultBrainBrain MappingCohort StudiesContrast MediaFemaleGadoliniumHumansImmunologic FactorsInterferon beta-1aMagnetic Resonance ImagingMaleMotor ActivityMultiple SclerosisContrast MediaGadoliniumImmunologic FactorsInterferon beta-1abrain plasticityfunctional MRIinflammationinterferon betamultiple sclerosis

Identifiers

PMID26991559
PMCPMC5069650
OpenAlexW2299892810

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.