Cargando…

Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control

OBJECTIVE: Functional connectivity MRI (fcMRI) studies of individuals currently diagnosed with major depressive disorder (MDD) document hyperconnectivities within the default mode network (DMN) and between the DMN and salience networks (SN) with regions of the cognitive control network (CCN). Studie...

Descripción completa

Detalles Bibliográficos
Autores principales: Jacobs, Rachel H., Jenkins, Lisanne M., Gabriel, Laura B., Barba, Alyssa, Ryan, Kelly A., Weisenbach, Sara L., Verges, Alvaro, Baker, Amanda M., Peters, Amy T., Crane, Natania A., Gotlib, Ian H., Zubieta, Jon-Kar, Phan, K. Luan, Langenecker, Scott A., Welsh, Robert C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146466/
https://www.ncbi.nlm.nih.gov/pubmed/25162661
http://dx.doi.org/10.1371/journal.pone.0104366
_version_ 1782332346951794688
author Jacobs, Rachel H.
Jenkins, Lisanne M.
Gabriel, Laura B.
Barba, Alyssa
Ryan, Kelly A.
Weisenbach, Sara L.
Verges, Alvaro
Baker, Amanda M.
Peters, Amy T.
Crane, Natania A.
Gotlib, Ian H.
Zubieta, Jon-Kar
Phan, K. Luan
Langenecker, Scott A.
Welsh, Robert C.
author_facet Jacobs, Rachel H.
Jenkins, Lisanne M.
Gabriel, Laura B.
Barba, Alyssa
Ryan, Kelly A.
Weisenbach, Sara L.
Verges, Alvaro
Baker, Amanda M.
Peters, Amy T.
Crane, Natania A.
Gotlib, Ian H.
Zubieta, Jon-Kar
Phan, K. Luan
Langenecker, Scott A.
Welsh, Robert C.
author_sort Jacobs, Rachel H.
collection PubMed
description OBJECTIVE: Functional connectivity MRI (fcMRI) studies of individuals currently diagnosed with major depressive disorder (MDD) document hyperconnectivities within the default mode network (DMN) and between the DMN and salience networks (SN) with regions of the cognitive control network (CCN). Studies of individuals in the remitted state are needed to address whether effects derive from trait, and not state or chronic burden features of MDD. METHOD: fcMRI data from two 3.0 Tesla GE scanners were collected from 30 unmedicated (47% medication naïve) youth (aged 18–23, modal depressive episodes = 1, mean age of onset = 16.2, SD = 2.6) with remitted MDD (rMDD; modal years well = 4) and compared with data from 23 healthy controls (HCs) using four bilateral seeds in the DMN and SN (posterior cingulate cortex (PCC), subgenual anterior cingulate (sgACC), and amygdala), followed by voxel-based comparisons of the whole brain. RESULTS: Compared to HCs, rMDD youth exhibited hyperconnectivities from both PCC and sgACC seeds with lateral, parietal, and frontal regions of the CCN, extending to the dorsal medial wall. A factor analysis reduced extracted data and a PCC factor was inversely correlated with rumination among rMDD youth. Two factors from the sgACC hyperconnectivity clusters were related to performance in cognitive control on a Go/NoGo task, one positively and one inversely. CONCLUSIONS: Findings document hyperconnectivities of the DMN and SN with the CCN (BA 8/10), which were related to rumination and sustained attention. Given these cognitive markers are known predictors of response and relapse, hyperconnectivities may increase relapse risk or represent compensatory mechanisms.
format Online
Article
Text
id pubmed-4146466
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-41464662014-08-29 Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control Jacobs, Rachel H. Jenkins, Lisanne M. Gabriel, Laura B. Barba, Alyssa Ryan, Kelly A. Weisenbach, Sara L. Verges, Alvaro Baker, Amanda M. Peters, Amy T. Crane, Natania A. Gotlib, Ian H. Zubieta, Jon-Kar Phan, K. Luan Langenecker, Scott A. Welsh, Robert C. PLoS One Research Article OBJECTIVE: Functional connectivity MRI (fcMRI) studies of individuals currently diagnosed with major depressive disorder (MDD) document hyperconnectivities within the default mode network (DMN) and between the DMN and salience networks (SN) with regions of the cognitive control network (CCN). Studies of individuals in the remitted state are needed to address whether effects derive from trait, and not state or chronic burden features of MDD. METHOD: fcMRI data from two 3.0 Tesla GE scanners were collected from 30 unmedicated (47% medication naïve) youth (aged 18–23, modal depressive episodes = 1, mean age of onset = 16.2, SD = 2.6) with remitted MDD (rMDD; modal years well = 4) and compared with data from 23 healthy controls (HCs) using four bilateral seeds in the DMN and SN (posterior cingulate cortex (PCC), subgenual anterior cingulate (sgACC), and amygdala), followed by voxel-based comparisons of the whole brain. RESULTS: Compared to HCs, rMDD youth exhibited hyperconnectivities from both PCC and sgACC seeds with lateral, parietal, and frontal regions of the CCN, extending to the dorsal medial wall. A factor analysis reduced extracted data and a PCC factor was inversely correlated with rumination among rMDD youth. Two factors from the sgACC hyperconnectivity clusters were related to performance in cognitive control on a Go/NoGo task, one positively and one inversely. CONCLUSIONS: Findings document hyperconnectivities of the DMN and SN with the CCN (BA 8/10), which were related to rumination and sustained attention. Given these cognitive markers are known predictors of response and relapse, hyperconnectivities may increase relapse risk or represent compensatory mechanisms. Public Library of Science 2014-08-27 /pmc/articles/PMC4146466/ /pubmed/25162661 http://dx.doi.org/10.1371/journal.pone.0104366 Text en © 2014 Jacobs et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jacobs, Rachel H.
Jenkins, Lisanne M.
Gabriel, Laura B.
Barba, Alyssa
Ryan, Kelly A.
Weisenbach, Sara L.
Verges, Alvaro
Baker, Amanda M.
Peters, Amy T.
Crane, Natania A.
Gotlib, Ian H.
Zubieta, Jon-Kar
Phan, K. Luan
Langenecker, Scott A.
Welsh, Robert C.
Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title_full Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title_fullStr Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title_full_unstemmed Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title_short Increased Coupling of Intrinsic Networks in Remitted Depressed Youth Predicts Rumination and Cognitive Control
title_sort increased coupling of intrinsic networks in remitted depressed youth predicts rumination and cognitive control
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4146466/
https://www.ncbi.nlm.nih.gov/pubmed/25162661
http://dx.doi.org/10.1371/journal.pone.0104366
work_keys_str_mv AT jacobsrachelh increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT jenkinslisannem increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT gabriellaurab increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT barbaalyssa increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT ryankellya increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT weisenbachsaral increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT vergesalvaro increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT bakeramandam increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT petersamyt increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT cranenataniaa increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT gotlibianh increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT zubietajonkar increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT phankluan increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT langeneckerscotta increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol
AT welshrobertc increasedcouplingofintrinsicnetworksinremitteddepressedyouthpredictsruminationandcognitivecontrol