Distinct functional connectivity phenotypes in preadolescent children with binge eating disorder by BMI status

Trevor Steward1, Kay Jann2, Stuart B Murray3

  • 1Melbourne School of Psychological Sciences, The University of Melbourne, Parkville, Victoria, Australia.

PubMed

Insights

Binge eating disorder (BED) in children shows altered brain connectivity, particularly between reward and default mode networks. These changes are linked to BED itself, not just weight status, impacting emotion regulation.

Area of Science:

  • Neuroscience
  • Child Psychiatry
  • Brain Imaging

Background:

  • Neurobiological mechanisms of pediatric binge eating disorder (BED) are unclear.
  • Alterations may stem from BED, obesity, or both.
  • Understanding these mechanisms is crucial for early intervention.

Purpose of the Study:

  • To investigate functional connectivity (FC) in inhibitory control and reward networks in children with and without BED.
  • To differentiate FC patterns based on Body Mass Index (BMI) within the BED group.
  • To clarify the specific neurobiological underpinnings of BED in preadolescence.

Main Methods:

  • Resting-state functional connectivity (FC) analysis using seed regions in prefrontal cortex, anterior cingulate cortex, posterior cingulate cortex, orbitofrontal cortex, nucleus accumbens, and amygdala.
  • Seed-to-voxel analyses compared FC in children with BED (high vs. low BMI) and controls.
  • Utilized data from the Adolescent Brain Cognitive Development (ABCD) Study.

Main Results:

  • Children with BED exhibited reduced connectivity between the reward network and default mode network regions, independent of BMI.
  • Hypoconnectivity was observed in fronto-amygdalar circuits in BED, linked to impaired emotion regulation.
  • These FC alterations appear specific to BED rather than obesity.

Conclusions:

  • Functional connectivity differences between reward and default mode networks are associated with BED in children.
  • These findings suggest BED, not weight status, is the primary driver of observed FC alterations.
  • The results highlight potential targets for understanding and treating pediatric BED.
Abstract

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