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Intrinsic neural circuitry of depression in adolescent females
Author(s) -
Jin Jingwen,
Van Snellenberg Jared X.,
Perlman Greg,
DeLorenzo Christine,
Klein Daniel N.,
Kotov Roman,
Mohanty Aprajita
Publication year - 2020
Publication title -
journal of child psychology and psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.652
H-Index - 211
eISSN - 1469-7610
pISSN - 0021-9630
DOI - 10.1111/jcpp.13123
Subject(s) - psychology , amygdala , prefrontal cortex , striatum , ventromedial prefrontal cortex , neuroscience , ventral striatum , depression (economics) , posterior cingulate , anterior cingulate cortex , biological neural network , cognition , dopamine , economics , macroeconomics
Background Adolescence is characterized by affective and cognitive changes that increase vulnerability to depression, especially in females. Neurodevelopmental models attribute adolescent depression to abnormal responses in amygdala, striatum, and prefrontal cortex (PFC). We examined whether the strength of functional brain networks involving these regions predicts depression symptoms in adolescent females. Methods In this longitudinal study, we recorded resting‐state functional connectivity (RSFC) in 174 adolescent females. Using a cross‐validation strategy, we related RSFC profiles that included (a) a network consisting of amygdala, striatum, and PFC ( within‐circuit model), (b) connectivity of this network to the whole brain ( extended‐circuit model), and (c) a network consisting of the entire brain ( whole‐brain model) to depression symptoms assessed concurrently and 18 months later. Results In testing subsets, the within‐circuit RSFC profiles were associated with depression symptoms concurrently and 18 months later, while the extended‐circuit and whole‐brain model did not explain any additional variance in depression symptoms. Connectivity related to anterior cingulate and ventromedial prefrontal cortex contributed most to the association. Conclusions Our results demonstrate that RSFC‐based brain networks that include amygdala, striatum, and PFC are stable neural signatures of concurrent and future depression symptoms, representing a significant step toward identifying the neural mechanism of depression in adolescence.

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