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Opportunity cost determines free-operant action initiation latency and predicts apathy

BACKGROUND: Apathy, a disabling and poorly understood neuropsychiatric symptom, is characterised by impaired self-initiated behaviour. It has been hypothesised that the opportunity cost of time (OCT) may be a key computational variable linking self-initiated behaviour with motivational status. OCT r...

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Autores principales: Nair, Akshay, Niyogi, Ritwik K., Shang, Fei, Tabrizi, Sarah J., Rees, Geraint, Rutledge, Robb B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106307/
https://www.ncbi.nlm.nih.gov/pubmed/37310334
http://dx.doi.org/10.1017/S0033291721003469
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author Nair, Akshay
Niyogi, Ritwik K.
Shang, Fei
Tabrizi, Sarah J.
Rees, Geraint
Rutledge, Robb B.
author_facet Nair, Akshay
Niyogi, Ritwik K.
Shang, Fei
Tabrizi, Sarah J.
Rees, Geraint
Rutledge, Robb B.
author_sort Nair, Akshay
collection PubMed
description BACKGROUND: Apathy, a disabling and poorly understood neuropsychiatric symptom, is characterised by impaired self-initiated behaviour. It has been hypothesised that the opportunity cost of time (OCT) may be a key computational variable linking self-initiated behaviour with motivational status. OCT represents the amount of reward which is foregone per second if no action is taken. Using a novel behavioural task and computational modelling, we investigated the relationship between OCT, self-initiation and apathy. We predicted that higher OCT would engender shorter action latencies, and that individuals with greater sensitivity to OCT would have higher behavioural apathy. METHODS: We modulated the OCT in a novel task called the ‘Fisherman Game’, Participants freely chose when to self-initiate actions to either collect rewards, or on occasion, to complete non-rewarding actions. We measured the relationship between action latencies, OCT and apathy for each participant across two independent non-clinical studies, one under laboratory conditions (n = 21) and one online (n = 90). ‘Average-reward’ reinforcement learning was used to model our data. We replicated our findings across both studies. RESULTS: We show that the latency of self-initiation is driven by changes in the OCT. Furthermore, we demonstrate, for the first time, that participants with higher apathy showed greater sensitivity to changes in OCT in younger adults. Our model shows that apathetic individuals experienced greatest change in subjective OCT during our task as a consequence of being more sensitive to rewards. CONCLUSIONS: Our results suggest that OCT is an important variable for determining free-operant action initiation and understanding apathy.
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spelling pubmed-101063072023-04-17 Opportunity cost determines free-operant action initiation latency and predicts apathy Nair, Akshay Niyogi, Ritwik K. Shang, Fei Tabrizi, Sarah J. Rees, Geraint Rutledge, Robb B. Psychol Med Original Article BACKGROUND: Apathy, a disabling and poorly understood neuropsychiatric symptom, is characterised by impaired self-initiated behaviour. It has been hypothesised that the opportunity cost of time (OCT) may be a key computational variable linking self-initiated behaviour with motivational status. OCT represents the amount of reward which is foregone per second if no action is taken. Using a novel behavioural task and computational modelling, we investigated the relationship between OCT, self-initiation and apathy. We predicted that higher OCT would engender shorter action latencies, and that individuals with greater sensitivity to OCT would have higher behavioural apathy. METHODS: We modulated the OCT in a novel task called the ‘Fisherman Game’, Participants freely chose when to self-initiate actions to either collect rewards, or on occasion, to complete non-rewarding actions. We measured the relationship between action latencies, OCT and apathy for each participant across two independent non-clinical studies, one under laboratory conditions (n = 21) and one online (n = 90). ‘Average-reward’ reinforcement learning was used to model our data. We replicated our findings across both studies. RESULTS: We show that the latency of self-initiation is driven by changes in the OCT. Furthermore, we demonstrate, for the first time, that participants with higher apathy showed greater sensitivity to changes in OCT in younger adults. Our model shows that apathetic individuals experienced greatest change in subjective OCT during our task as a consequence of being more sensitive to rewards. CONCLUSIONS: Our results suggest that OCT is an important variable for determining free-operant action initiation and understanding apathy. Cambridge University Press 2023-04 2021-10-12 /pmc/articles/PMC10106307/ /pubmed/37310334 http://dx.doi.org/10.1017/S0033291721003469 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
Nair, Akshay
Niyogi, Ritwik K.
Shang, Fei
Tabrizi, Sarah J.
Rees, Geraint
Rutledge, Robb B.
Opportunity cost determines free-operant action initiation latency and predicts apathy
title Opportunity cost determines free-operant action initiation latency and predicts apathy
title_full Opportunity cost determines free-operant action initiation latency and predicts apathy
title_fullStr Opportunity cost determines free-operant action initiation latency and predicts apathy
title_full_unstemmed Opportunity cost determines free-operant action initiation latency and predicts apathy
title_short Opportunity cost determines free-operant action initiation latency and predicts apathy
title_sort opportunity cost determines free-operant action initiation latency and predicts apathy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10106307/
https://www.ncbi.nlm.nih.gov/pubmed/37310334
http://dx.doi.org/10.1017/S0033291721003469
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