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Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis

BACKGROUND: Depression is characterised partly by blunted reactions to reward. However, tasks probing this deficiency have not distinguished insensitivity to reward from insensitivity to the prediction errors for reward that determine learning and are putatively reported by the phasic activity of do...

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Autores principales: Huys, Quentin JM, Pizzagalli, Diego A, Bogdan, Ryan, Dayan, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701611/
https://www.ncbi.nlm.nih.gov/pubmed/23782813
http://dx.doi.org/10.1186/2045-5380-3-12
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author Huys, Quentin JM
Pizzagalli, Diego A
Bogdan, Ryan
Dayan, Peter
author_facet Huys, Quentin JM
Pizzagalli, Diego A
Bogdan, Ryan
Dayan, Peter
author_sort Huys, Quentin JM
collection PubMed
description BACKGROUND: Depression is characterised partly by blunted reactions to reward. However, tasks probing this deficiency have not distinguished insensitivity to reward from insensitivity to the prediction errors for reward that determine learning and are putatively reported by the phasic activity of dopamine neurons. We attempted to disentangle these factors with respect to anhedonia in the context of stress, Major Depressive Disorder (MDD), Bipolar Disorder (BPD) and a dopaminergic challenge. METHODS: Six behavioural datasets involving 392 experimental sessions were subjected to a model-based, Bayesian meta-analysis. Participants across all six studies performed a probabilistic reward task that used an asymmetric reinforcement schedule to assess reward learning. Healthy controls were tested under baseline conditions, stress or after receiving the dopamine D(2) agonist pramipexole. In addition, participants with current or past MDD or BPD were evaluated. Reinforcement learning models isolated the contributions of variation in reward sensitivity and learning rate. RESULTS: MDD and anhedonia reduced reward sensitivity more than they affected the learning rate, while a low dose of the dopamine D(2) agonist pramipexole showed the opposite pattern. Stress led to a pattern consistent with a mixed effect on reward sensitivity and learning rate. CONCLUSION: Reward-related learning reflected at least two partially separable contributions. The first related to phasic prediction error signalling, and was preferentially modulated by a low dose of the dopamine agonist pramipexole. The second related directly to reward sensitivity, and was preferentially reduced in MDD and anhedonia. Stress altered both components. Collectively, these findings highlight the contribution of model-based reinforcement learning meta-analysis for dissecting anhedonic behavior.
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spelling pubmed-37016112013-07-10 Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis Huys, Quentin JM Pizzagalli, Diego A Bogdan, Ryan Dayan, Peter Biol Mood Anxiety Disord Research BACKGROUND: Depression is characterised partly by blunted reactions to reward. However, tasks probing this deficiency have not distinguished insensitivity to reward from insensitivity to the prediction errors for reward that determine learning and are putatively reported by the phasic activity of dopamine neurons. We attempted to disentangle these factors with respect to anhedonia in the context of stress, Major Depressive Disorder (MDD), Bipolar Disorder (BPD) and a dopaminergic challenge. METHODS: Six behavioural datasets involving 392 experimental sessions were subjected to a model-based, Bayesian meta-analysis. Participants across all six studies performed a probabilistic reward task that used an asymmetric reinforcement schedule to assess reward learning. Healthy controls were tested under baseline conditions, stress or after receiving the dopamine D(2) agonist pramipexole. In addition, participants with current or past MDD or BPD were evaluated. Reinforcement learning models isolated the contributions of variation in reward sensitivity and learning rate. RESULTS: MDD and anhedonia reduced reward sensitivity more than they affected the learning rate, while a low dose of the dopamine D(2) agonist pramipexole showed the opposite pattern. Stress led to a pattern consistent with a mixed effect on reward sensitivity and learning rate. CONCLUSION: Reward-related learning reflected at least two partially separable contributions. The first related to phasic prediction error signalling, and was preferentially modulated by a low dose of the dopamine agonist pramipexole. The second related directly to reward sensitivity, and was preferentially reduced in MDD and anhedonia. Stress altered both components. Collectively, these findings highlight the contribution of model-based reinforcement learning meta-analysis for dissecting anhedonic behavior. BioMed Central 2013-06-19 /pmc/articles/PMC3701611/ /pubmed/23782813 http://dx.doi.org/10.1186/2045-5380-3-12 Text en Copyright © 2013 Huys et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Huys, Quentin JM
Pizzagalli, Diego A
Bogdan, Ryan
Dayan, Peter
Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title_full Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title_fullStr Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title_full_unstemmed Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title_short Mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
title_sort mapping anhedonia onto reinforcement learning: a behavioural meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701611/
https://www.ncbi.nlm.nih.gov/pubmed/23782813
http://dx.doi.org/10.1186/2045-5380-3-12
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