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Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease
Negative and positive emotions are known to shape decision-making toward more or less impulsive responses, respectively. Decision-making and emotion processing are underpinned by shared brain regions including the ventromedial prefrontal cortex (vmPFC) and the amygdala. How these processes interact...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393308/ https://www.ncbi.nlm.nih.gov/pubmed/32613246 http://dx.doi.org/10.1093/scan/nsaa085 |
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author | Manuel, Aurélie L Roquet, Daniel Landin-Romero, Ramon Kumfor, Fiona Ahmed, Rebekah M Hodges, John R Piguet, Olivier |
author_facet | Manuel, Aurélie L Roquet, Daniel Landin-Romero, Ramon Kumfor, Fiona Ahmed, Rebekah M Hodges, John R Piguet, Olivier |
author_sort | Manuel, Aurélie L |
collection | PubMed |
description | Negative and positive emotions are known to shape decision-making toward more or less impulsive responses, respectively. Decision-making and emotion processing are underpinned by shared brain regions including the ventromedial prefrontal cortex (vmPFC) and the amygdala. How these processes interact at the behavioral and brain levels is still unclear. We used a lesion model to address this question. Study participants included individuals diagnosed with behavioral-variant frontotemporal dementia (bvFTD, n = 18), who typically present deficits in decision-making/emotion processing and atrophy of the vmPFC, individuals with Alzheimer’s disease (AD, n = 12) who present with atrophy in limbic structures and age-matched healthy controls (CTRL, n = 15). Prior to each choice on the delay discounting task participants were cued with a positive, negative or neutral picture and asked to vividly imagine witnessing the event. As hypothesized, our findings showed that bvFTD patients were more impulsive than AD patients and CTRL and did not show any emotion-related modulation of delay discounting rate. In contrast, AD patients showed increased impulsivity when primed by negative emotion. This increased impulsivity was associated with reduced integrity of bilateral amygdala in AD but not in bvFTD. Altogether, our results indicate that decision-making and emotion interact at the level of the amygdala supporting findings from animal studies. |
format | Online Article Text |
id | pubmed-7393308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-73933082020-08-04 Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease Manuel, Aurélie L Roquet, Daniel Landin-Romero, Ramon Kumfor, Fiona Ahmed, Rebekah M Hodges, John R Piguet, Olivier Soc Cogn Affect Neurosci Original Manuscript Negative and positive emotions are known to shape decision-making toward more or less impulsive responses, respectively. Decision-making and emotion processing are underpinned by shared brain regions including the ventromedial prefrontal cortex (vmPFC) and the amygdala. How these processes interact at the behavioral and brain levels is still unclear. We used a lesion model to address this question. Study participants included individuals diagnosed with behavioral-variant frontotemporal dementia (bvFTD, n = 18), who typically present deficits in decision-making/emotion processing and atrophy of the vmPFC, individuals with Alzheimer’s disease (AD, n = 12) who present with atrophy in limbic structures and age-matched healthy controls (CTRL, n = 15). Prior to each choice on the delay discounting task participants were cued with a positive, negative or neutral picture and asked to vividly imagine witnessing the event. As hypothesized, our findings showed that bvFTD patients were more impulsive than AD patients and CTRL and did not show any emotion-related modulation of delay discounting rate. In contrast, AD patients showed increased impulsivity when primed by negative emotion. This increased impulsivity was associated with reduced integrity of bilateral amygdala in AD but not in bvFTD. Altogether, our results indicate that decision-making and emotion interact at the level of the amygdala supporting findings from animal studies. Oxford University Press 2020-07-01 /pmc/articles/PMC7393308/ /pubmed/32613246 http://dx.doi.org/10.1093/scan/nsaa085 Text en © The Author(s) 2020. Published by Oxford University Press. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Manuscript Manuel, Aurélie L Roquet, Daniel Landin-Romero, Ramon Kumfor, Fiona Ahmed, Rebekah M Hodges, John R Piguet, Olivier Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title | Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title_full | Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title_fullStr | Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title_full_unstemmed | Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title_short | Interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and Alzheimer’s disease |
title_sort | interactions between decision-making and emotion in behavioral-variant frontotemporal dementia and alzheimer’s disease |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7393308/ https://www.ncbi.nlm.nih.gov/pubmed/32613246 http://dx.doi.org/10.1093/scan/nsaa085 |
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