Evidence map›Paper›PMID 27513853›Full record

ArticlePloS one2016

The Relationship between Gray Matter Quantitative MRI and Disability in Secondary Progressive Multiple Sclerosis.

René-Maxime Gracien, Alina Jurcoane, Marlies Wagner, Sarah C Reitz, Christoph Mayer, Steffen Volz, Stephanie-Michelle Hof, Vinzenz Fleischer, Amgad Droby, Helmuth Steinmetz and 4 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2016. 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
0.7field-weighted citation impact, top 27% 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, 18 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

14 authors at 3 institutions in 2 countries.

René-Maxime GracienDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Alina JurcoaneDepartment of Neuroradiology, Goethe University, Frankfurt/Main, Germany.
Marlies WagnerDepartment of Neuroradiology, Goethe University, Frankfurt/Main, Germany.
Sarah C ReitzDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Christoph MayerDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Steffen VolzBrain Imaging Center, Goethe University, Frankfurt/Main, Germany.
Stephanie-Michelle HofDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Vinzenz FleischerDepartment of Neurology, Johannes Gutenberg University, Mainz, Germany.
Amgad DrobyDepartment of Neurology, Johannes Gutenberg University, Mainz, Germany.
Helmuth SteinmetzDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Frauke ZippDepartment of Neurology, Johannes Gutenberg University, Mainz, Germany.
Elke HattingenDepartment of Neuroradiology, Goethe University, Frankfurt/Main, Germany.
Ralf DeichmannBrain Imaging Center, Goethe University, Frankfurt/Main, Germany.
Johannes C KleinDepartment of Neurology, Goethe University, Frankfurt/Main, Germany.
Goethe University Frankfurt · DEJohannes Gutenberg University Mainz · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn secondary progressive Multiple Sclerosis (SPMS), global neurodegeneration as a driver of disability gains importance in comparison to focal inflammatory processes. However, clinical MRI does not visualize changes of tissue composition outside MS lesions. This quantitative MRI (qMRI) study investigated cortical and deep gray matter (GM) proton density (PD) values and T1 relaxation times to explore their potential to assess neuronal damage and its relationship to clinical disability in SPMS. MATERIALS AND

methods11 SPMS patients underwent quantitative T1 and PD mapping. Parameter values across the cerebral cortex and deep GM structures were compared with 11 healthy controls, and correlation with disability was investigated for regions exhibiting significant group differences.

resultsPD was increased in the whole GM, cerebral cortex, thalamus, putamen and pallidum. PD correlated with disability in the whole GM, cerebral cortex, putamen and pallidum. T1 relaxation time was prolonged and correlated with disability in the whole GM and cerebral cortex.

conclusionOur study suggests that the qMRI parameters GM PD (which likely indicates replacement of neural tissue with water) and cortical T1 (which reflects cortical damage including and beyond increased water content) are promising qMRI candidates for the assessment of disease status, and are related to disability in SPMS.

Indexed as

AdultCase-Control StudiesCerebral CortexFemaleGray MatterHumansIntellectual DisabilityMagnetic Resonance ImagingMaleMultiple Sclerosis, Chronic Progressive

Identifiers

PMID27513853
PMCPMC4981438
OpenAlexW2514453661

What OpenQuestion holds

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LicenceCC BY
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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.