Evidence map›Paper›PMID 32795963›Full record

ArticleNeuroImage. Clinical2020

Microstructural changes in the reward system are associated with post-stroke depression.

Lena K L Oestreich, Paul Wright, Michael J O'Sullivan

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

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  14. Pathomechanisms of Vascular Depression in Older Adults.International journal of molecular sciences · 2021
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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

3 authors at 3 institutions in 2 countries.

Lena K L OestreichUQ Centre for Clinical Research, The University of Queensland, Brisbane, Australia; Centre for Advanced Imaging, The University of Queensland, Brisbane, Australia. Electronic address: l.oestreich@uq.edu.au.
Paul WrightDepartment of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK.
Michael J O'SullivanUQ Centre for Clinical Research, The University of Queensland, Brisbane, Australia; Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK; Department of Neurology, Royal Brisbane and Women's Hospital, Brisbane, Australia; Herston Imaging Research Facility, Royal Brisbane and Women's Hospital, Brisbane, Australia.
ARC Centre of Excellence in Advanced Molecular Imaging · AUKing's College London · GBUniversity of Queensland · AU

Funding

Medical Research Council MR/K022113/1
6 · The paper itself

Abstract

backgroundStudies of lesion location have been unsuccessful in identifying mappings between single brain regions and post-stroke depression (PSD). Based on studies implicating the reward system in major depressive disorder without stroke, we investigated structural correlates within this system and their associations with PSD.

methodsThe study enrolled 16 healthy controls, 12 stroke patients with PSD and 34 stroke patients free of PSD. Participants underwent 3T structural and diffusion MRI. Graph theoretical measures were used to examine global topology and whole-brain connectome analyses were employed to assess differences in the interregional connectivity matrix between groups. Structural correlates specific to the reward system were examined from grey matter volumes and by reconstructing its main white matter pathways, namely the medial forebrain bundle and cingulum connections, using deterministic tractography. Fractional anisotropy (FA) was derived as a measure of microstructural organization, and extracellular free-water (FW) as a possible proxy of neuroinflammation.

resultsSubnetworks of decreased FA-weighted and increased FW-weighted connectivity were observed in patients with PSD relative to healthy controls. These networks subsumed the majority of regions constituting the reward system. Within the reward system, FA and FW of major connection pathways and grey matter volume were collectively predictive of PSD, explaining 37.8% of the variance in depression severity.

conclusionsPSD is associated with grey matter volume loss, reduced FA and increased extracellular FW in the reward system, similar to features observed in major depression without stroke. Structural characterization of the reward system is a promising biomarker of vulnerability to depression after stroke.

Indexed as

Major Depressive DisorderRewardStrokeWhite MatterAgedDepressionDiffusion Tensor ImagingFemaleHumansMaleMiddle AgedConnectomeGrey matterMagnetic resonance imaging (MRI)NeuroinflammationPost-stroke depression (PSD)White matter

Identifiers

PMID32795963
PMCPMC7426585
OpenAlexW3044852739

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.