Evidence map›Paper›PMID 25893491›Full record

ArticleJournal of neuroimaging : official journal of the American Society of Neuroimaging

Correlation of Brain Atrophy, Disability, and Spinal Cord Atrophy in a Murine Model of Multiple Sclerosis.

M Mateo Paz Soldán, Mekala R Raman, Jeffrey D Gamez, Anne K Lohrey, Yi Chen, Istvan Pirko, Aaron J Johnson

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of neuroimaging : official journal of the American Society of Neuroimaging. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 19 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

7 authors at 2 institutions in 1 country.

M Mateo Paz SoldánDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Mekala R RamanDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Jeffrey D GamezDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Anne K LohreyDepartment of Neurology, University of Cincinnati, Cincinnati, Ohio.
Yi ChenDepartment of Neurology, University of Cincinnati, Cincinnati, Ohio.
Istvan PirkoDepartment of Neurology, Mayo Clinic, Rochester, Minnesota.
Aaron J JohnsonDepartment of Immunology, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · USUniversity of Cincinnati · US

Funding

CD 8 T Cell Mediated Disruption of Blood Brain Tight JunctionR01NS060881 · NINDS · UNIVERSITY OF CINCINNATI · PI JOHNSON, AARON J · 2009 to 2013
$1.7M
CD8+ T cells in formation of T1 black holes in animal model of multiple sclerosisR01NS058698 · NINDS · UNIVERSITY OF CINCINNATI · PI PIRKO, ISTVAN · 2008 to 2011
$1.2M
NINDS NIH HHS R01 NS058698NINDS NIH HHS R01 NS060881NINDS NIH HHS R01NS58698NINDS NIH HHS R01NS60881
6 · The paper itself

Abstract

backgroundDisability progression in multiple sclerosis (MS) remains incompletely understood. Unlike lesional measures, central nervous system atrophy has a strong correlation with disability. Theiler's murine encephalomyelitis virus infection in SJL/J mice is an established model of progressive MS. We utilized in vivo MRI to quantify brain and spinal cord atrophy in this model and analyzed the temporal relationship between atrophy and disability.

methodsInfected and control mice were followed for 12 months. Disability was assessed periodically using rotarod assay. Volumetric MRI datasets were acquired at 7 Tesla. Ventricular volume and C4-5 spinal cord cross-sectional area measurements were performed using Analyze 10.

resultsAt 3 months, brain atrophy reached statistical significance (P = .005). In contrast, disability did not differ until 4 months post-infection (P = .0005). Cord atrophy reached significance by 9 months (P = 0.009). By 12 months, brain atrophy resulted in 111.8% increased ventricular volume (P = .00003), while spinal cord cross-sectional area was 25.6% reduced (P = .001) among cases.

conclusionsOur results suggest that significant brain atrophy precedes and predicts the development of disability, while spinal cord atrophy occurs late and correlates with severe disability. The observed temporal relationship establishes a framework for mechanisms of disability progression and enables further investigations of their underlying substrate.

Indexed as

AnimalsAtrophyBrainDisease ProgressionMagnetic Resonance ImagingMiceMovement DisordersMultiple Sclerosis, Chronic ProgressiveSpinal CordStatistics as Topicatrophydisabilitymagnetic resonance imagingMultiple sclerosis

Identifiers

PMID25893491
PMCPMC4506196
OpenAlexW2128459314

What OpenQuestion holds

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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.