Dorsal ACC activation reduced in youths with disruptive behaviour disorder during reward anticipation

13 Apr 2021
Dorsal ACC activation reduced in youths with disruptive behaviour disorder during reward anticipation

Adolescents with disruptive behaviour disorder (DBD), with and without callous-unemotional (CU) traits, have reduced dorsal anterior cingulate cortex (ACC) activation during reward anticipation relative to typically developing youths, a study has shown.

The investigators obtained data from the Adolescent Brain and Cognitive Development Study (mean age 9.51 years, 49 percent female). They examined reward-related activation during the monetary incentive delay task across 16 brain regions, including the amygdala, ACC, nucleus accumbens (NAcc), and orbitofrontal cortex (OFC). Network-level coactivation was examined using latent variable modeling.

The investigators compared the following diagnostic groups: typically developing youths (n=693) and youths with DBDs (n=995), subdivided into those with CU traits (DBD+CU, N=198) and without CU traits (DBD only, N=276).

Youths in the overall DBD group, with and without CU traits, demonstrated decreased dorsal ACC activation compared with typically developing individuals during reward anticipation. The DBD-only group had reduced ventral and dorsal striatal activity relative to the DBD+CU and typically developing groups.

During reward receipt, adolescents with DBDs exhibited increased cortical (eg, OFC) and subcortical (eg, NAcc) regional activation compared with typically developing youths. The DBD+CU group also showed greater activation in several regions than those in the typically developing (eg, amygdala) and DBD-only (eg, dorsal ACC) groups.

At the network level, the DBD-only group demonstrated decreased anticipatory reward activation relative to the typically developing and DBD+CU groups. On the other hand, those in the DBD+CU group had increased activation during reward receipt as opposed to typically developing youths.

“These findings advance our understanding of unique neuro-aetiologic pathways to DBDs and CU traits,” the investigators said.

Am J Psychiatry 2021;178:333-342