Evidence map›Paper›PMID 31467520›Full record

ArticleNeural plasticity2019

Correlated Resting-State Functional MRI Activity of Frontostriatal, Thalamic, Temporal, and Cerebellar Brain Regions Differentiates Stroke Survivors with High Compared to Low Depressive Symptom Scores.

Peter Goodin, Gemma Lamp, Rishma Vidyasagar, Alan Connelly, Stephen Rose, Bruce C V Campbell, Tamara Tse, Henry Ma, David Howells, Graeme J Hankey and 3 more

Open access · goldAbstract read
In one paragraph

Article in Neural plasticity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Observational
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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 8 institutions in 1 country.

Peter GoodinNeurorehabilitation and Recovery, Stroke, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.
Gemma LampNeurorehabilitation and Recovery, Stroke, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.
Rishma VidyasagarNeurorehabilitation and Recovery, Stroke, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.
Alan ConnellyAdvanced Imaging, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.
Stephen RoseAustralian e-Health Research Centre, CSIRO, Brisbane, Queensland, Australia.
Bruce C V CampbellDepartment of Medicine and Neurology, Melbourne Brain Centre, Royal Melbourne Hospital, Parkville, Melbourne, Victoria, Australia.
Tamara TseNeurorehabilitation and Recovery, Stroke, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.ORCID 0000-0002-7136-5037
Henry MaDepartment of Medicine, School of Clinical Sciences, Monash University, Clayton, Victoria, Australia.
David HowellsDepartment of Florey, University of Melbourne, Parkville, Victoria, Australia.
Graeme J HankeyMedical School, University of Western Australia, Perth, Western Australia, Australia.ORCID 0000-0002-6044-7328
Stephen DavisDepartment of Medicine and Neurology, Melbourne Brain Centre, Royal Melbourne Hospital, Parkville, Melbourne, Victoria, Australia.
Geoffrey DonnanDepartment of Florey, University of Melbourne, Parkville, Victoria, Australia.
Leeanne M CareyNeurorehabilitation and Recovery, Stroke, Florey Institute of Neuroscience and Mental Health, Melbourne Brain Centre-Austin Campus, Heidelberg, Victoria, Australia.ORCID 0000-0001-6376-8613
Florey Institute of Neuroscience and Mental Health · AUThe Royal Melbourne Hospital · AUThe University of Melbourne · AUCommonwealth Scientific and Industrial Research Organisation · AULa Trobe University · AUMonash University · AUThe University of Western Australia · AUUniversity of Tasmania · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: One in three survivors of stroke experience poststroke depression (PSD). PSD has been linked with poorer recovery of function and cognition, yet our understanding of potential mechanisms is currently limited. Alterations in resting-state functional MRI have been investigated to a limited extent. Fluctuations in low frequency signal are reported, but it is unknown if interactions are present between the level of depressive symptom score and intrinsic brain activity in varying brain regions. Objective: To investigate potential interaction effects between whole-brain resting-state activity and depressive symptoms in stroke survivors with low and high levels of depressive symptoms. Methods: A cross-sectional analysis of 63 stroke survivors who were assessed at 3 months poststroke for depression, using the Montgomery-Åsberg Depression Rating Scale (MÅDRS-SIGMA), and for brain activity using fMRI. A MÅDRS-SIGMA score of >8 was classified as high depressive symptoms. Fractional amplitude of frequency fluctuations (fALFF) data across three frequency bands (broadband, i.e., ~0.01-0.08; subbands, i.e., slow-5: ~0.01-0.027 Hz, slow-4: 0.027-0.07) was examined. Results: Of the 63 stroke survivors, 38 were classified as "low-depressive symptoms" and 25 as "high depressive symptoms." Six had a past history of depression. We found interaction effects across frequency bands in several brain regions that differentiated the two groups. The broadband analysis revealed interaction effects in the left insula and the left superior temporal lobe. The subband analysis showed contrasting fALFF response between the two groups in the left thalamus, right caudate, and left cerebellum. Across the three frequency bands, we found contrasting fALFF response in areas within the fronto-limbic-thalamic network and cerebellum. Conclusions: We provide evidence that fALFF is sensitive to changes in poststroke depressive symptom severity and implicates frontostriatal and cerebellar regions, consistent with previous studies. The use of multiband analysis could be an effective method to examine neural correlates of depression after stroke. The START-PrePARE trial is registered with the Australian New Zealand Clinical Trial Registry, number ACTRN12610000987066.

Indexed as

AgedBrainBrain MappingCross-Sectional StudiesDepressionDiagnosis, DifferentialFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedSeverity of Illness IndexStrokeSurvivors

Identifiers

PMID31467520
PMCPMC6701282
OpenAlexW2965675757

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.