4.4 Article

A graph theory-based whole brain approach to assess mood state differences in adolescents and young adults with bipolar disorder

Journal

BIPOLAR DISORDERS
Volume 24, Issue 4, Pages 412-423

Publisher

WILEY
DOI: 10.1111/bdi.13144

Keywords

adolescent; bipolar disorder; depression; fMRI; functional connectivity; mood state

Funding

  1. Brain and Behavior Research Foundation
  2. National Center for Advancing Translational Sciences [TL1TR001864]
  3. International Bipolar Foundation
  4. National Institute of Mental Health [RC1MH088366, R01MH070902, R01MH69747, R61MH111929, UG3MH111929]
  5. Klingenstein Third Generation Foundation
  6. American Foundation for Suicide Prevention [SRG-1-10-119, SRG-0-017-13]
  7. John and Hope Furth Endowment
  8. AIM Youth Mental Health

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Using a whole-brain Intrinsic Connectivity Distribution approach, hubs of brain dysfunction were identified in adolescents and young adults with Bipolar I Disorder, particularly showing higher connectivity in depressed states, which were closely related to mood symptoms and could be potential targets for early intervention.
Objectives Identifying hubs of brain dysfunction in adolescents and young adults with Bipolar I Disorder (BDAYA) could provide targets for early detection, prevention, and treatment. Previous neuroimaging studies across mood states of BDAYA are scarce and often examined limited brain regions potentially prohibiting detection of other important regions. We used a data-driven whole-brain Intrinsic Connectivity Distribution (ICD) approach to investigate dysconnectivity hubs across mood states in BDAYA. Methods Functional magnetic resonance imaging whole-brain ICD data were investigated for differences across four groups: BDAYA-depressed (n = 22), BDAYA-euthymic (n = 45), BDAYA-elevated (n = 24), and healthy controls (HC, n = 111). Clusters of ICD differences were assessed for regional dysconnectivity and mood symptom relationships. Analyses were also performed for BDAYA overall (vs. HC) ICD differences persisting across mood states. Results ICD was higher in the BDAYA- depressed group than other groups in bilateral ventral/rostral/dorsal prefrontal cortex (PFC) and right lenticular nucleus (LN) (p(corrected) <0.05). In BDAYA-depressed, functional connectivity (FC) was increased between these regions with their contralateral homologues and PFC-medial temporal FC was more negative (p < 0.005). PFC-related findings correlated with depression scores (p < 0.05). The overall BDAYA group showed ICD increases in more ventral left PFC and right cerebellum, present across euthymia and acute mood states. Conclusions This ICD approach supports a PFC hub of inter- and intra-hemispheric frontotemporal dysconnectivity in BDAYA with potential trait features and disturbances of higher magnitude during depression. Hubs were also revealed in LN and cerebellum, less common foci of BD research. The hubs are potential targets for early interventions to detect, prevent, and treat BD.

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