Differentiating brain function of punishment versus reward processing in conduct disorder with and without attention deficit hyperactivity disorder
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
Abstract
OBJECTIVES: Conduct disorder (CD) and attention-deficit/hyperactivity disorder (ADHD) are reported to co-occur in about 30-50% of affected individuals. Research suggests that poor reinforcement-based decision-making may contribute to impaired social functioning in both youths with CD and ADHD. Considering its frequent co-occurrence this raises the question whether decision-making deficits in both disorders have a disorder-specific and/or shared neurobiological basis.
METHODS: 138 participants with CD, ADHD, or CD + ADHD, and typically developing controls (TDCs) aged 9-18 years (48% girls) were included in the study. Participants completed a reinforcement-based decision-making task in the fMRI scanner, investigating decision-making capabilities under different reinforcement contingencies (i.e. punishment vs. reward). Whole-brain and ROI analyses were used to test for potential group differences.
RESULTS: For punishment versus reward contingencies, relative to TDCs, youths with CD + ADHD displayed lower brain activity in dorsal striatum (incl. caudate), middle temporal gyrus (MTG), inferior frontal gyrus (IFG) and lateral occipital cortex, and they showed lower activity in dorsal striatum (incl. putamen), orbitofrontal cortex (OFC) and IFG relative to participants with ADHD. All other group comparisons were found to be non-significant.
CONCLUSIONS: Participants with comorbid CD + ADHD are neurobiologically the most severely impaired group regarding reinforcement-based decision-making, particularly in response to punishment.
Details
Original language | English |
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Pages (from-to) | 1-12 |
Number of pages | 12 |
Journal | World Journal of Biological Psychiatry |
Volume | 23 |
Issue number | 5 |
Publication status | E-pub ahead of print - 15 Nov 2021 |
Peer-reviewed | Yes |
External IDs
Scopus | 85119449343 |
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ORCID | /0000-0003-2408-2939/work/172085998 |