TY - JOUR
T1 - The neurobiology of personal control during reward learning and its relation to mood
AU - Romaniuk, Liana
AU - Sandu, Anca-larisa
AU - Waiter, Gordon D.
AU - Mcneil, Christopher J.
AU - Xueyi, Shen
AU - Harris, Matthew A.
AU - Macfarlane, Jennifer A.
AU - Lawrie, Stephen M.
AU - Deary, Ian J.
AU - Murray, Alison D.
AU - Delgado, Mauricio R.
AU - Steele, J Douglas
AU - Mcintosh, Andrew M.
AU - Whalley, Heather C.
N1 - Copyright © 2018 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.
PY - 2019/2
Y1 - 2019/2
N2 - Background
The majority of reward learning neuroimaging studies have not focussed on the motivational aspects of behaviour, such as the inherent value placed on choice itself. The experience and affective value of personal control may have particular relevance for psychiatric disorders including depression.
Methods/Design
In this study, we adapted an fMRI reward task that probed the value placed on exerting control over one’s decisions, termed ‘choice value’, in 122 healthy participants. We examined activation associated with choice value; personally-chosen versus passively-received rewards; and reinforcement learning metrics such as prediction error. Relationships were tested between measures of motivational orientation (categorised as Autonomy, Control and Impersonal), and subclinical depressive symptomatology.
Results
Anticipating personal choice activated left insula, cingulate, right inferior frontal cortex and ventral striatum (P<0.05 FWE-corrected). Ventral striatal activations to choice were diminished in those with subclinical depressive symptomatology. Personally-chosen rewards were associated with greater activation of the insula/IFG, cingulate cortex, hippocampus, thalamus and substantia nigra compared to rewards that were passively received. In people who felt little control over their own behaviour (Impersonal orientation), prediction error signals in nucleus accumbens were stronger during passive trials.
Discussion
Previous finding regarding personal choice have been verified, and taken forward through the use of both reinforcement learning models, and correlations with psychopathology. Personal choice has an impact on the extended reward network, potentially allowing these clinically-important areas to be addressed in ways more relevant to personality styles, self-esteem and symptoms such as motivational anhedonia.
AB - Background
The majority of reward learning neuroimaging studies have not focussed on the motivational aspects of behaviour, such as the inherent value placed on choice itself. The experience and affective value of personal control may have particular relevance for psychiatric disorders including depression.
Methods/Design
In this study, we adapted an fMRI reward task that probed the value placed on exerting control over one’s decisions, termed ‘choice value’, in 122 healthy participants. We examined activation associated with choice value; personally-chosen versus passively-received rewards; and reinforcement learning metrics such as prediction error. Relationships were tested between measures of motivational orientation (categorised as Autonomy, Control and Impersonal), and subclinical depressive symptomatology.
Results
Anticipating personal choice activated left insula, cingulate, right inferior frontal cortex and ventral striatum (P<0.05 FWE-corrected). Ventral striatal activations to choice were diminished in those with subclinical depressive symptomatology. Personally-chosen rewards were associated with greater activation of the insula/IFG, cingulate cortex, hippocampus, thalamus and substantia nigra compared to rewards that were passively received. In people who felt little control over their own behaviour (Impersonal orientation), prediction error signals in nucleus accumbens were stronger during passive trials.
Discussion
Previous finding regarding personal choice have been verified, and taken forward through the use of both reinforcement learning models, and correlations with psychopathology. Personal choice has an impact on the extended reward network, potentially allowing these clinically-important areas to be addressed in ways more relevant to personality styles, self-esteem and symptoms such as motivational anhedonia.
U2 - 10.1016/j.bpsc.2018.09.015
DO - 10.1016/j.bpsc.2018.09.015
M3 - Article
C2 - 30470583
SN - 2451-9022
VL - 4
SP - 190
EP - 199
JO - Biological psychiatry. Cognitive neuroscience and neuroimaging
JF - Biological psychiatry. Cognitive neuroscience and neuroimaging
IS - 2
ER -