Literature DB >> 29322687

Abnormal fronto-striatal activation as a marker of threshold and subthreshold Bulimia Nervosa.

Marilyn Cyr1, Xiao Yang1, Guillermo Horga2, Rachel Marsh1.   

Abstract

This study aimed to determine whether functional disturbances in fronto-striatal control circuits characterize adolescents with Bulimia Nervosa (BN) spectrum eating disorders regardless of clinical severity. FMRI was used to assess conflict-related brain activations during performance of a Simon task in two samples of adolescents with BN symptoms compared with healthy adolescents. The BN samples differed in the severity of their clinical presentation, illness duration and age. Multi-voxel pattern analyses (MVPAs) based on machine learning were used to determine whether patterns of fronto-striatal activation characterized adolescents with BN spectrum disorders regardless of clinical severity, and whether accurate classification of less symptomatic adolescents (subthreshold BN; SBN) could be achieved based on patterns of activation in adolescents who met DSM5 criteria for BN. MVPA classification analyses revealed that both BN and SBN adolescents could be accurately discriminated from healthy adolescents based on fronto-striatal activation. Notably, the patterns detected in more severely ill BN compared with healthy adolescents accurately discriminated less symptomatic SBN from healthy adolescents. Deficient activation of fronto-striatal circuits can characterize BN early in its course, when clinical presentations are less severe, perhaps pointing to circuit-based disturbances as useful biomarker or risk factor for the disorder, and a tool for understanding its developmental trajectory, as well as the development of early interventions.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Bulimia Nervosa; Simon task; adolescents; conflict resolution; fronto-striatal circuits; functional magnetic resonance imaging; machine learning; multi-voxel pattern analysis; self-regulatory control

Mesh:

Year:  2018        PMID: 29322687      PMCID: PMC5847471          DOI: 10.1002/hbm.23955

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


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