Neural mechanisms of inhibitory control in preadolescent irritability: Insights from the ABCD study

Biol Psychol. 2024 Oct:192:108856. doi: 10.1016/j.biopsycho.2024.108856. Epub 2024 Aug 16.

Abstract

Objective: Elevated pediatric irritability is a transdiagnostic symptom that predicts multiple mental health problems in adolescence and adulthood. Altered top-down regulatory networks, such as inhibitory control networks that suppress an impulse in favor of goal-directed behavior, are thought to contribute to high levels of youth irritability. Nevertheless, little work has examined links between youth irritability and neural processes supporting inhibitory control in large diverse samples, nor have they focused on the key period ramping up to adolescence (i.e., preadolescence).

Method: Functional MRI data from 5380 preadolescents (age M=9.97 years, SD=0.62) in the baseline Adolescent Brain and Cognitive Development (ABCD) Study were analyzed. Parents reported on their preadolescent's irritability. The stop signal task (SST) was leveraged to probe successful and failed inhibitory control. Activation and functional connectivity with amygdala, ventral striatum, and prefrontal seed regions were calculated during the SST and used in whole brain and region of interest (ROI) group-level analyses evaluating irritability effects.

Results: Preadolescents with higher levels of irritability displayed decreases in functional connectivity among amygdala, ventral striatum, and prefrontal cortex regions during both successful and failed inhibitory control conditions. These results remained after adjusting for co-occurring anxiety, depression, and attention-deficit/hyperactivity symptoms.

Conclusions: Findings suggest neural aberrations in inhibitory control play a role in the pathophysiology of preadolescent irritability and associations are not merely due to co-occurring symptoms. Neural mechanisms of inhibitory control associated with irritability may provide novel intervention targets.

Keywords: Brain; Inhibition; Irritability; Preadolescence; Psychopathology.

MeSH terms

  • Adolescent
  • Amygdala / diagnostic imaging
  • Amygdala / physiology
  • Amygdala / physiopathology
  • Brain / diagnostic imaging
  • Brain / physiology
  • Brain / physiopathology
  • Brain Mapping
  • Child
  • Executive Function / physiology
  • Female
  • Humans
  • Inhibition, Psychological*
  • Irritable Mood* / physiology
  • Magnetic Resonance Imaging*
  • Male
  • Neural Pathways / diagnostic imaging
  • Neural Pathways / physiology
  • Neural Pathways / physiopathology
  • Prefrontal Cortex / diagnostic imaging
  • Prefrontal Cortex / physiology
  • Prefrontal Cortex / physiopathology
  • Ventral Striatum / diagnostic imaging
  • Ventral Striatum / physiology
  • Ventral Striatum / physiopathology