Abstract

A recently developed risk calculator for bipolar disorder (BD) accounts for clinical and parental psychopathology. Yet, it is understood that both familial predisposition and early life adversity contribute to the development of BD. How the interplay between these two factors influence emotion and reward processing networks in youth at risk for BD remains unclear. In this exploratory analysis, offspring of BD parents performed emotion and reward processing tasks while undergoing a fMRI scan. Risk calculator score was used to assess risk for developing BD in the next 5 years. Environmental risk was tabulated using the Stressful Life Events Schedule (SLES). Emotion and reward processing networks were investigated for genetic and/or environment interactions. Interaction effects were found between risk calculator scores, negative SLES score and activity in right amygdala and bilateral fusiform gyri during the emotion processing task, as well as activity in the fronto-, striatal, and parietal regions during the reward processing task. Our findings are preliminary; however, they support the unique and interactive contributions of both familial and environmental risk factors on emotion and reward processing within OBP. They also identify potential neural targets to guide development of interventions for youth at greatest risk for psychiatric disorders.

Highlights

  • Neurodevelopmental models for Bipolar Disorder (BD) posit the involvement of both genetic predisposition, such as having a parent diagnosed with BD, and life stressors, such as early life adversity [1]

  • Our main findings support our hypothesis that OBP at highest risk of developing BD in the 5 years, based on predictive risk calculator score, and greater number of recent negative stressful life events (SLEs) showed the greatest alterations within the functioning of these emotion and reward processing circuits

  • Higher probability for developing BD in the future was associated with more positive associations between greater exposure to negative SLEs was associated with greater activity in right amygdala, and bilateral fusiform

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Summary

Introduction

Neurodevelopmental models for Bipolar Disorder (BD) posit the involvement of both genetic predisposition, such as having a parent diagnosed with BD, and life stressors, such as early life adversity [1]. OBP showed differential patterns of pregenual ACC-vlPFC connectivity: reduced during reward anticipation, and increased during loss anticipation, relative to healthy control youth [47] Taken together, these studies indicate aberrant activity and connectivity in emotion and reward processing neural circuits in OBP, which may represent neural markers of risk for future BD. We hypothesized that relative to healthy youth offspring of healthy parents, the greatest magnitude of abnormal functioning of emotion and reward processing circuits, in particular in amygdala, VS and prefrontal cortical regions would be observed in OBP with highest predictive risk, as assessed by the risk calculator, and with the greatest exposure to negative SLEs

Methods
Participants
Results
Functional Connectivity during Emotion Processing task
Discussion
Full Text
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