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A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value

In decision-making situations individuals rarely have complete information available to select the best option and often show decisional randomness, i.e. given the same amount of knowledge individuals choose different options at different times. Dysfunctional processes resulting in altered decisiona...

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Autores principales: Howlett, Jonathon R., Paulus, Martin P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377428/
https://www.ncbi.nlm.nih.gov/pubmed/32702026
http://dx.doi.org/10.1371/journal.pone.0233761
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author Howlett, Jonathon R.
Paulus, Martin P.
author_facet Howlett, Jonathon R.
Paulus, Martin P.
author_sort Howlett, Jonathon R.
collection PubMed
description In decision-making situations individuals rarely have complete information available to select the best option and often show decisional randomness, i.e. given the same amount of knowledge individuals choose different options at different times. Dysfunctional processes resulting in altered decisional randomness can be considered a target process for psychiatric disorders, yet these processes remain poorly understood. Advances in computational modeling of decision-making offer a potential explanation for decisional randomness by positing that decisions are implemented in the brain through accumulation of noisy evidence, causing a generally less preferred option to be chosen at times by chance. One such model, the linear ballistic accumulator (LBA), assumes that individuals accumulate information for each option independently over time and that the first option to reach a threshold will be selected. To investigate the mechanisms of decisional randomness, we applied the LBA to a decision-making task in which risk and expected value (EV) were explicitly signaled prior to making a choice, and estimated separate drift rates for each of the four task stimuli (representing high and low EV and high and low risk). We then used the fitted LBA parameters to predict subject response rates on held-out trials for each of the 6 possible stimulus pairs. We found that choices predicted by LBA were correlated with actual choices across subjects for all stimulus pairs. Taken together, these findings suggest that sequential sampling models can account for decisional randomness on an explicit probabilistic task, which may have implications for understanding decision-making in healthy individuals and in psychiatric populations.
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spelling pubmed-73774282020-07-27 A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value Howlett, Jonathon R. Paulus, Martin P. PLoS One Research Article In decision-making situations individuals rarely have complete information available to select the best option and often show decisional randomness, i.e. given the same amount of knowledge individuals choose different options at different times. Dysfunctional processes resulting in altered decisional randomness can be considered a target process for psychiatric disorders, yet these processes remain poorly understood. Advances in computational modeling of decision-making offer a potential explanation for decisional randomness by positing that decisions are implemented in the brain through accumulation of noisy evidence, causing a generally less preferred option to be chosen at times by chance. One such model, the linear ballistic accumulator (LBA), assumes that individuals accumulate information for each option independently over time and that the first option to reach a threshold will be selected. To investigate the mechanisms of decisional randomness, we applied the LBA to a decision-making task in which risk and expected value (EV) were explicitly signaled prior to making a choice, and estimated separate drift rates for each of the four task stimuli (representing high and low EV and high and low risk). We then used the fitted LBA parameters to predict subject response rates on held-out trials for each of the 6 possible stimulus pairs. We found that choices predicted by LBA were correlated with actual choices across subjects for all stimulus pairs. Taken together, these findings suggest that sequential sampling models can account for decisional randomness on an explicit probabilistic task, which may have implications for understanding decision-making in healthy individuals and in psychiatric populations. Public Library of Science 2020-07-23 /pmc/articles/PMC7377428/ /pubmed/32702026 http://dx.doi.org/10.1371/journal.pone.0233761 Text en © 2020 Howlett, Paulus http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Howlett, Jonathon R.
Paulus, Martin P.
A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title_full A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title_fullStr A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title_full_unstemmed A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title_short A parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
title_sort parallel accumulator model accounts for decision randomness when deciding on risky prospects with different expected value
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377428/
https://www.ncbi.nlm.nih.gov/pubmed/32702026
http://dx.doi.org/10.1371/journal.pone.0233761
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