Evidence map›Paper›PMID 37672593›Full record

ArticleHuman brain mapping2023

Depression recurrence is accompanied by longer periods in default mode and more frequent attentional and reward processing dynamic brain-states during resting-state activity.

Sonsoles Alonso, Anna Tyborowska, Nessa Ikani, Roel J T Mocking, Caroline A Figueroa, Aart H Schene, Gustavo Deco, Morten L Kringelbach, Joana Cabral, Henricus G Ruhé

Abstract read
In one paragraph

Article in Human brain mapping, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

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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

10 authors.

Sonsoles AlonsoDepartment of Biomedical Sciences of Cells and Systems, Cognitive Neuroscience Center, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.ORCID 0000-0001-9631-6664
Anna TyborowskaDepartment of Psychiatry, Radboud University Medical Centre, Nijmegen, the Netherlands.ORCID 0000-0002-7621-3497
Nessa IkaniDepartment of Psychiatry, Radboud University Medical Centre, Nijmegen, the Netherlands.ORCID 0000-0002-4466-5421
Roel J T MockingDepartment of Psychiatry, Amsterdam UMC, Location AMC, Amsterdam, the Netherlands.ORCID 0000-0003-3543-3810
Caroline A FigueroaDepartment of Psychiatry, University Medical Centre Utrecht, Utrecht, the Netherlands.ORCID 0000-0003-0692-2244
Aart H ScheneDepartment of Psychiatry, Radboud University Medical Centre, Nijmegen, the Netherlands.
Gustavo DecoDepartment of Information and Communication Technologies, Center for Brain and Cognition, Computational Neuroscience Group, Universitat Pompeu Fabra, Barcelona, Spain.ORCID 0000-0002-8995-7583
Morten L KringelbachCentre for Eudaimonia and Human Flourishing, Linacre College, University of Oxford, Oxford, UK.ORCID 0000-0002-3908-6898
Joana CabralCentre for Eudaimonia and Human Flourishing, Linacre College, University of Oxford, Oxford, UK.ORCID 0000-0002-6715-0826
Henricus G RuhéDepartment of Psychiatry, Radboud University Medical Centre, Nijmegen, the Netherlands.ORCID 0000-0001-6072-0358

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recurrence in major depressive disorder (MDD) is common, but neurobiological models capturing vulnerability for recurrences are scarce. Disturbances in multiple resting-state networks have been linked to MDD, but most approaches focus on stable (vs. dynamic) network characteristics. We investigated how the brain's dynamical repertoire changes after patients transition from remission to recurrence of a new depressive episode. Sixty two drug-free, MDD-patients with ≥2 episodes underwent a baseline resting-state fMRI scan when in remission. Over 30-months follow-up, 11 patients with a recurrence and 17 matched-remitted MDD-patients without a recurrence underwent a second fMRI scan. Recurrent patterns of functional connectivity were characterized by applying Leading Eigenvector Dynamics Analysis (LEiDA). Differences between baseline and follow-up were identified for the 11 non-remitted patients, while data from the 17 matched-remitted patients was used as a validation dataset. After the transition into a depressive state, basal ganglia-anterior cingulate cortex (ACC) and visuo-attentional networks were detected significantly more often, whereas default mode network activity was found to have a longer duration. Additionally, the fMRI signal in the basal ganglia-ACC areas underlying the reward network, were significantly less synchronized with the rest of the brain after recurrence (compared to a state of remission). No significant changes were observed in the matched-remitted patients who were scanned twice while in remission. These findings characterize changes that may be associated with the transition from remission to recurrence and provide initial evidence of altered dynamical exploration of the brain's repertoire of functional networks when a recurrent depressive episode occurs.

Indexed as

Major Depressive DisorderBrainBrain MappingDepressionHumansMagnetic Resonance ImagingRewarddynamic functional connectivityMDDrecurrenceresting-state fMRI

Identifiers

PMID37672593
PMCPMC10619399

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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.