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dc.contributor.authorHirshfeld-Becker, Dina
dc.contributor.authorBiederman, Joseph
dc.contributor.authorUchida, Mai
dc.contributor.authorKenworthy, Tara
dc.contributor.authorBrown, Ariel
dc.contributor.authorKagan, Elana
dc.contributor.authorChai, Xiaoqian
dc.contributor.authorDoehrmann, Oliver
dc.contributor.authorLeonard, Julia
dc.contributor.authorSalvatore, John J.
dc.contributor.authorde los Angeles, Carlo S
dc.contributor.authorGabrieli, John D. E.
dc.contributor.authorWhitfield-Gabrieli, Susan
dc.date.accessioned2017-12-08T15:53:49Z
dc.date.available2017-12-08T15:53:49Z
dc.date.issued2015-12
dc.date.submitted2015-12
dc.identifier.issn0006-3223
dc.identifier.urihttp://hdl.handle.net/1721.1/112654
dc.description.abstractBackground Neuroimaging studies of patients with major depression have revealed abnormal intrinsic functional connectivity measured during the resting state in multiple distributed networks. However, it is unclear whether these findings reflect the state of major depression or reflect trait neurobiological underpinnings of risk for major depression. Methods We compared resting-state functional connectivity, measured with functional magnetic resonance imaging, between unaffected children of parents who had documented histories of major depression (at-risk, n = 27; 8–14 years of age) and age-matched children of parents with no lifetime history of depression (control subjects, n = 16). Results At-risk children exhibited hyperconnectivity between the default mode network and subgenual anterior cingulate cortex/orbital frontal cortex, and the magnitude of connectivity positively correlated with individual symptom scores. At-risk children also exhibited 1) hypoconnectivity within the cognitive control network, which also lacked the typical anticorrelation with the default mode network; 2) hypoconnectivity between left dorsolateral prefrontal cortex and subgenual anterior cingulate cortex; and 3) hyperconnectivity between the right amygdala and right inferior frontal gyrus, a key region for top-down modulation of emotion. Classification between at-risk children and control subjects based on resting-state connectivity yielded high accuracy with high sensitivity and specificity that was superior to clinical rating scales. Conclusions Children at familial risk for depression exhibited atypical functional connectivity in the default mode, cognitive control, and affective networks. Such task-independent functional brain measures of risk for depression in children could be used to promote early intervention to reduce the likelihood of developing depression.en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.BIOPSYCH.2015.12.003en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleAltered Intrinsic Functional Brain Architecture in Children at Familial Risk of Major Depressionen_US
dc.typeArticleen_US
dc.identifier.citationChai, Xiaoqian J. et al. “Altered Intrinsic Functional Brain Architecture in Children at Familial Risk of Major Depression.” Biological Psychiatry 80, 11 (December 2016): 849–858 © 2016 Society of Biological Psychiatryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.mitauthorChai, Xiaoqian
dc.contributor.mitauthorDoehrmann, Oliver
dc.contributor.mitauthorLeonard, Julia
dc.contributor.mitauthorSalvatore, John J.
dc.contributor.mitauthorde los Angeles, Carlo S
dc.contributor.mitauthorGabrieli, John D. E.
dc.contributor.mitauthorWhitfield-Gabrieli, Susan
dc.relation.journalBiological Psychiatryen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2017-12-07T19:38:01Z
dspace.orderedauthorsChai, Xiaoqian J.; Hirshfeld-Becker, Dina; Biederman, Joseph; Uchida, Mai; Doehrmann, Oliver; Leonard, Julia A.; Salvatore, John; Kenworthy, Tara; Brown, Ariel; Kagan, Elana; de los Angeles, Carlo; Gabrieli, John D.E.; Whitfield-Gabrieli, Susanen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-5946-1069
dc.identifier.orcidhttps://orcid.org/0000-0001-8099-2721
dc.identifier.orcidhttps://orcid.org/0000-0003-1158-5692
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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