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dc.contributor.authorRoberts, H
dc.contributor.authorSchreiner, MW
dc.contributor.authorPocius, S
dc.contributor.authorDillahunt, AK
dc.contributor.authorFarstead, B
dc.contributor.authorFeldman, D
dc.contributor.authorBessette, KL
dc.contributor.authorKaufman, EA
dc.contributor.authorSlattery, W
dc.contributor.authorJacobs, RH
dc.contributor.authorJago, D
dc.contributor.authorCrowell, SE
dc.contributor.authorWatkins, ER
dc.contributor.authorLangenecker, SA
dc.date.accessioned2024-01-17T16:13:11Z
dc.date.issued2024-01-10
dc.date.updated2024-01-17T14:31:48Z
dc.description.abstractBackground: Trait rumination is a habitual response to negative experiences that can emerge during adolescence, increasing risk of depression. Trait rumination is correlated with poor inhibitory control (IC) and altered default mode network (DMN) and cognitive control network (CCN) engagement. Provoking state rumination in high ruminating youth permits investigation of rumination and IC at the neural level, highlighting potential treatment targets. Methods: Fifty-three high-ruminating youth were cued with an unresolved goal that provoked state rumination, then completed a modified Sustained Attention to Response Task (SART) that measures IC (commissions on no-go trials) in a functional MRI study. Thought probes measured state rumination about that unresolved goal and task-focused thoughts during the SART. Results: Greater state rumination during the SART was correlated with more IC failures. CCN engagement increased during rumination (relative to task-focus), including left dorsolateral prefrontal cortex and dorsal-medial prefrontal cortex. Relative to successful response suppression, DMN engagement increased during IC failures amongst individuals with higher state and trait rumination. Exploratory analyses suggested more bothersome unresolved goals predicted higher left DLPFC activation during rumination. Limitations: The correlational research design did not permit a direct contrast of causal accounts of the relationship between rumination and IC. Conclusions: State rumination was associated with impaired IC and disrupted modulation of DMN and CCN. Increased CCN engagement during rumination suggested effortful suppression of negative thoughts, and this was greater for more bothersome unresolved goals. Relative task disengagement was observed during rumination-related errors. DMN-CCN dysregulation in high-ruminating youth may be an important treatment target.en_GB
dc.description.sponsorshipNational Institute of Mental Healthen_GB
dc.identifier.citationVol. 16, article 100729en_GB
dc.identifier.doihttps://doi.org/10.1016/j.jadr.2024.100729
dc.identifier.grantnumberMH116080en_GB
dc.identifier.urihttp://hdl.handle.net/10871/135045
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rights© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)en_GB
dc.subjectRuminationen_GB
dc.subjectDepressionen_GB
dc.subjectExecutive functionsen_GB
dc.subjectDefault-mode networken_GB
dc.subjectCognitive control networken_GB
dc.subjectAdolescenceen_GB
dc.titleState rumination predicts inhibitory control failures and dysregulation of default, salience, and cognitive control networks in youth at risk of depressive relapse: Findings from the RuMeChange trialen_GB
dc.typeArticleen_GB
dc.date.available2024-01-17T16:13:11Z
dc.identifier.issn2666-9153
exeter.article-number100729
dc.descriptionThis is the final version. Available on open access from Elsevier via the DOI in this record. en_GB
dc.identifier.journalJournal of Affective Disorders Reportsen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2024-01-09
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2024-01-10
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2024-01-17T16:05:29Z
refterms.versionFCDVoR
refterms.dateFOA2024-01-17T16:13:20Z
refterms.panelAen_GB
refterms.dateFirstOnline2024-01-10


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© 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
Except where otherwise noted, this item's licence is described as © 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)