4.4 Article

Neural changes in youth at high risk for bipolar disorder undergoing family-focused therapy or psychoeducation

Journal

BIPOLAR DISORDERS
Volume 23, Issue 6, Pages 604-614

Publisher

WILEY
DOI: 10.1111/bdi.13045

Keywords

mood disorder; neuroimaging; psychotherapy; youth

Funding

  1. National Institute of Mental Health [K01MH097769, R01MH093666, R01MN093676]
  2. Brain and Behavior Research Foundation

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This study used fMRI to investigate the impact of FFT-HR treatment on emotion processing networks in youth at high risk for bipolar disorder. The results showed increased activation in the dorsolateral prefrontal cortex in the FFT-HR group post-treatment, while activation decreased in the EC group. Additionally, decreasing activation in the hippocampus and amygdala was correlated with improvement in hypomania, while increasing activation in the DLPFC was correlated with improvement in depression.
Background Patients with mood disorders may benefit from psychosocial interventions through changes in brain networks underlying emotion processing. In this study, we used functional magnetic resonance imaging (fMRI) to investigate treatment-related changes in emotion processing networks in youth at familial high risk for bipolar disorder (BD). Methods Youth, ages 9-17, were randomly assigned to family-focused therapy for high-risk youth (FFT-HR) or an active comparison treatment, Enhanced Care (EC). Before and after these 4-month treatments, participants underwent fMRI while viewing happy, fearful, and calm facial expressions. Twenty youth in FFT-HR and 20 in EC were included in analyses of pre- to post-treatment changes in activation across the whole brain. Significant clusters were assessed for correlation with mood symptom improvement. Results In the dorsolateral prefrontal cortex (DLPFC), activation increased from pre- to post-treatment in the FFT-HR group and decreased in the EC group. Insula activation decreased in the FFT-HR group and did not change in the EC group. Across both treatments, decreasing activation in the hippocampus and amygdala was correlated with pre- to post-treatment improvement in hypomania, while increasing activation in the DLPFC was correlated with pre- to post-treatment improvement in depression. Discussion Psychosocial treatment addresses abnormalities in emotion regulation networks in youth at high risk for BD. Increased prefrontal cortex activation suggests enhanced emotion regulation from pre- to post-treatment with FFT-HR. Improvements in family interactions may facilitate the development of prefrontal resources that provide protection against future mood episodes.

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