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. 2017 Jul:216:36-45.
doi: 10.1016/j.jad.2016.11.042. Epub 2016 Dec 1.

Neural correlates of RDoC reward constructs in adolescents with diverse psychiatric symptoms: A Reward Flanker Task pilot study

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Neural correlates of RDoC reward constructs in adolescents with diverse psychiatric symptoms: A Reward Flanker Task pilot study

Kailyn A L Bradley et al. J Affect Disord. 2017 Jul.

Abstract

Background: There has been growing interest under the Research Domain Criteria initiative to investigate behavioral constructs and their underlying neural circuitry. Abnormalities in reward processes are salient across psychiatric conditions and may precede future psychopathology in youth. However, the neural circuitry underlying such deficits has not been well defined. Therefore, in this pilot, we studied youth with diverse psychiatric symptoms and examined the neural underpinnings of reward anticipation, attainment, and positive prediction error (PPE, unexpected reward gain). Clinically, we focused on anhedonia, known to reflect deficits in reward function.

Methods: Twenty-two psychotropic medication-free youth, 16 with psychiatric symptoms, exhibiting a full range of anhedonia, were scanned during the Reward Flanker Task. Anhedonia severity was quantified using the Snaith-Hamilton Pleasure Scale. Functional magnetic resonance imaging analyses were false discovery rate corrected for multiple comparisons.

Results: Anticipation activated a broad network, including the medial frontal cortex and ventral striatum, while attainment activated memory and emotion-related regions such as the hippocampus and parahippocampal gyrus, but not the ventral striatum. PPE activated a right-dominant fronto-temporo-parietal network. Anhedonia was only correlated with activation of the right angular gyrus during anticipation and the left precuneus during PPE at an uncorrected threshold.

Limitations: Findings are preliminary due to the small sample size.

Conclusions: This pilot characterized the neural circuitry underlying different aspects of reward processing in youth with diverse psychiatric symptoms. These results highlight the complexity of the neural circuitry underlying reward anticipation, attainment, and PPE. Furthermore, this study underscores the importance of RDoC research in youth.

Keywords: Adolescence; Anhedonia; Positive valence system; RDoC; fMRI.

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Figures

Figure 1
Figure 1
Reward Flanker Task (RFT). Depiction of an example trial on the RFT.
Figure 2
Figure 2
A) Neural activation during reward anticipation vs. reward attainment. B) Neural activation during reward attainment vs. reward anticipation. For 2A and 2B, p-value maps from the permutation testing with threshold-free cluster enhancement analyses are presented; p-values are false discovery rate (FDR) corrected for multiple comparisons (p < .05). C) Depiction of the p-value maps from 2A and 2B overlaid on one another to show differences between the contrasts, with blue (dark gray) = reward anticipation vs. reward attainment and yellow (light gray) = reward attainment vs. reward anticipation. VS = ventral striatum
Figure 2
Figure 2
A) Neural activation during reward anticipation vs. reward attainment. B) Neural activation during reward attainment vs. reward anticipation. For 2A and 2B, p-value maps from the permutation testing with threshold-free cluster enhancement analyses are presented; p-values are false discovery rate (FDR) corrected for multiple comparisons (p < .05). C) Depiction of the p-value maps from 2A and 2B overlaid on one another to show differences between the contrasts, with blue (dark gray) = reward anticipation vs. reward attainment and yellow (light gray) = reward attainment vs. reward anticipation. VS = ventral striatum
Figure 3
Figure 3
Neural activation during positive prediction error (PPE). PPE was defined as unexpected reward attainment (correct feedback from trials with an unknown cue ‘?’ worth 10¢ and 50¢) vs. expected reward attainment (correct feedback from trials with a known cue worth 10¢ and 50¢). Images depict p-value maps from the permutation testing with threshold-free cluster enhancement analyses; p-values are false discovery rate (FDR) corrected for multiple comparisons (p < .05).

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