Neuroimaging Evidence for Right Orbitofrontal Cortex Differences in Adolescents With Emotional and Behavioral Dysregulation

  • Philip A Spechler
  • Bader Chaarani
  • Catherine Orr
  • Scott Mackey
  • Stephen T Higgins
  • Tobias Banaschewski
  • Arun L W Bokde
  • Uli Bromberg
  • Christian Büchel
  • Erin Burke Quinlan
  • Patricia J Conrod
  • Sylvane Desrivières
  • Herta Flor
  • Vincent Frouin
  • Penny Gowland
  • Andreas Heinz
  • Bernd Ittermann
  • Jean-Luc Martinot
  • Frauke Nees
  • Dimitri Papadopoulos Orfanos
  • Luise Poustka
  • Juliane H Fröhner
  • Michael N Smolka
  • Henrik Walter
  • Robert Whelan
  • Gunter Schumann
  • Hugh Garavan
  • Robert R Althoff
  • IMAGEN Consortium

Related Research units

Abstract

OBJECTIVE: To characterize the structural and functional neurobiology of a large group of adolescents exhibiting a behaviorally and emotionally dysregulated phenotype.

METHOD: Adolescents aged 14 years from the IMAGEN study were investigated. Latent class analysis (LCA) on the Strengths and Difficulties Questionnaire (SDQ) was used to identify a class of individuals with elevated behavioral and emotional difficulties ("dysregulated"; n = 233) who were compared to a matched sample from a low symptom class (controls, n = 233). Whole-brain gray matter volume (GMV) images were compared using a general linear model with 10,000 random label permutations. Regional GMV findings were then probed for functional differences from three functional magnetic resonance imaging (fMRI) tasks. Significant brain features then informed mediation path models linking the likelihood of psychiatric disorders (DSM-IV) with dysregulation.

RESULTS: Whole-brain differences were found in the right orbitofrontal cortex (R.OFC; p < .05; k = 48), with dysregulated individuals exhibiting lower GMV. The dysregulated group also exhibited higher activity in this region during successful inhibitory control (F1,429 = 7.53, p < .05). Path analyses indicated significant direct effects between the likelihood of psychopathologies and dysregulation. Modeling the R.OFC as a mediator returned modest partial effects, suggesting that the path linking the likelihood of an anxiety or conduct disorder diagnoses to dysregulation is partially explained by this anatomical feature.

CONCLUSION: A large sample of dysregulated adolescents exhibited lower GMV in the R.OFC relative to controls. Dysregulated individuals also exhibited higher regional activations when exercising inhibitory control at performance levels comparable to those of controls. These findings suggest a neurobiological marker of dysregulation and highlight the role of the R.OFC in impaired emotional and behavioral control.

Bibliographical data

Original languageEnglish
ISSN0890-8567
DOIs
Publication statusPublished - 11.2019
PubMed 31004740