Abstract

ObjectivesCurrent research suggests significant disruptions in functional brain networks in individuals with mood disorder, and in those at familial risk. Studies of structural brain networks provide important insights into synchronized maturational change but have received less attention. We aimed to investigate developmental relationships of large‐scale brain networks in mood disorder using structural covariance (SC) analyses.MethodsWe conducted SC analysis of baseline structural imaging data from 121 at the time of scanning unaffected high risk (HR) individuals (29 later developed mood disorder after a median time of 4.95 years), and 89 healthy controls (C‐well) with no familial risk from the Scottish Bipolar Family Study (age 15‐27, 64% female). Voxel‐wise analyses of covariance were conducted to compare the associations between each seed region in visual, auditory, motor, speech, semantic, executive‐control, salience and default‐mode networks and the whole brain signal. SC maps were compared for (a) HR(all) versus C‐well individuals, and (b) between those who remained well (HR‐well), versus those who subsequently developed mood disorder (HR‐MD), and C‐well.ResultsThere were no significant differences between HR(all) and C‐well individuals. On splitting the HR group based on subsequent clinical outcome, the HR‐MD group however displayed greater baseline SC in the salience and executive‐control network, and HR‐well individuals showed less SC in the salience network, compared to C‐well, respectively (P < .001).ConclusionsThese findings indicate differences in network‐level inter‐regional relationships, especially within the salience network, which precede onset of mood disorder in those at familial risk.

Highlights

  • Bipolar disorder (BD) is a highly heritable affective disorder characterized by intense fluctuations in mood, and is one of the leading causes of disability worldwide.[1]

  • We found no significant differences in structural covariance (SC) when comparing all individuals with a family history of mood disorder and C-well, and when comparing those at familial risk who developed mood disorder with those who did not over the follow up

  • We found no significant differences in unaffected individuals at familial risk of mood disorder compared to controls

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Summary

Introduction

Bipolar disorder (BD) is a highly heritable affective disorder characterized by intense fluctuations in mood, and is one of the leading causes of disability worldwide.[1]. Our group previously demonstrated subtle but significant changes in structural brain networks prior to psychosis onset in ultra-high risk individuals using this approach.[12] While in adult depression there have been indications of decreased SC in the salience network (SN)[13] and default-mode network (DMN), and higher levels of SC in the emotion regulation network versus controls,[14] it is unclear, if these are present prior to onset of disorder

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