Literature DB >> 25416726

Mapping the relationship between subgenual cingulate cortex functional connectivity and depressive symptoms across adolescence.

Cherie Strikwerda-Brown1, Christopher G Davey2, Sarah Whittle1, Nicholas B Allen2, Michelle L Byrne1, Orli S Schwartz1, Julian G Simmons1, Dominic Dwyer1, Ben J Harrison3.   

Abstract

Changes in the functional connectivity of the subgenual anterior cingulate cortex (SGC) have been linked with depressive symptoms. The aim of this study was to map this relationship across mid to late adolescence. Employing a longitudinal functional magnetic resonance imaging (fMRI) design, associations between patterns of resting-state SGC functional connectivity and symptoms of depression were examined at two time points in an initial sample of 72 adolescents. Using a region-of-interest approach, these associations were evaluated cross-sectionally and longitudinally. Cross-sectionally, weaker SGC functional connectivity with the posterior cingulate cortex (PCC), angular gyrus and dorsal prefrontal cortex at baseline, and weaker SGC connectivity with the dorsomedial prefrontal cortex (DMPFC) and ventromedial prefrontal cortex at follow-up, were associated with higher depressive symptoms. Longitudinally, a decrease in SGC functional connectivity with DMPFC, PCC, angular gyrus and middle temporal gyrus was associated with higher depressive symptoms at follow-up. The observation of weaker SGC connectivity predicting increased symptoms contrasts with the majority of resting-state fMRI studies in clinically depressed populations. Taken together with these past studies, our findings suggest depression-related changes in SGC functional connectivity may differ across developmental and illness stages.
© The Author (2014). Published by Oxford University Press. For Permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  adolescence; depression; fMRI; functional connectivity; subgenual cingulate cortex

Mesh:

Year:  2014        PMID: 25416726      PMCID: PMC4483565          DOI: 10.1093/scan/nsu143

Source DB:  PubMed          Journal:  Soc Cogn Affect Neurosci        ISSN: 1749-5016            Impact factor:   3.436


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