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Neural response during explicit and implicit face processing varies developmentally in bipolar disorder.

Christen M Deveney1, Melissa A Brotman2, Laura A Thomas2

  • 1Emotion and Development Branch, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA, Section on the Neurobiology and Treatment of Mood Disorders, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA, and Scientific and Statistical Computing Core, Department of Health and Human Services, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA cdeveney@wellesley.edu.

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Summary

Children and adults with bipolar disorder (BD) show similar face emotion processing deficits and amygdala dysfunction. These neural abnormalities may serve as biomarkers for BD across development.

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Area of Science:

  • Neuroscience
  • Psychiatry
  • Developmental Psychology

Background:

  • Bipolar disorder (BD) affects both children and adults, presenting with challenges in recognizing facial emotions and altered neural responses.
  • Direct comparisons between pediatric and adult BD populations are limited, hindering understanding of BD's developmental course.

Purpose of the Study:

  • To directly compare face emotion processing and neural circuitry function in children and adults with BD versus healthy controls.
  • To investigate the developmental trajectory of neural abnormalities associated with BD.

Main Methods:

  • Functional magnetic resonance imaging (fMRI) was used to compare 41 individuals with BD (19 children, 22 adults) and 44 healthy controls (25 children, 19 adults).
  • Participants performed explicit and implicit judgments on angry and happy face morphs varying in emotional intensity.

Main Results:

  • Individuals with BD, regardless of age, demonstrated a failure to recruit the amygdala in response to increasing anger intensity.
  • Subgenual anterior cingulate modulation deficits were present in both child and adult BD patients, linked to implicit and explicit processing, respectively.
  • The observed amygdala response difference was not significant in euthymic youth or those without ADHD, possibly due to reduced statistical power.

Conclusions:

  • Face emotion labeling deficits and associated neural circuitry dysfunction, particularly involving the amygdala and subgenual anterior cingulate, are present in bipolar disorder across development.
  • These abnormalities may represent potential neuroimaging biomarkers for BD, detectable from childhood through adulthood.