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Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage

The amygdala is believed to play a major role in orienting attention towards threat-related stimuli. However, behavioral studies on amygdala-damaged patients have given inconsistent results—variously reporting decreased, persisted, and increased attention towards threat. Here we aimed to characteriz...

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Autores principales: Pishnamazi, Morteza, Tafakhori, Abbas, Loloee, Sogol, Modabbernia, Amirhossein, Aghamollaii, Vajiheh, Bahrami, Bahador, Winston, Joel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Masson 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962776/
https://www.ncbi.nlm.nih.gov/pubmed/27173975
http://dx.doi.org/10.1016/j.cortex.2016.04.012
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author Pishnamazi, Morteza
Tafakhori, Abbas
Loloee, Sogol
Modabbernia, Amirhossein
Aghamollaii, Vajiheh
Bahrami, Bahador
Winston, Joel S.
author_facet Pishnamazi, Morteza
Tafakhori, Abbas
Loloee, Sogol
Modabbernia, Amirhossein
Aghamollaii, Vajiheh
Bahrami, Bahador
Winston, Joel S.
author_sort Pishnamazi, Morteza
collection PubMed
description The amygdala is believed to play a major role in orienting attention towards threat-related stimuli. However, behavioral studies on amygdala-damaged patients have given inconsistent results—variously reporting decreased, persisted, and increased attention towards threat. Here we aimed to characterize the impact of developmental amygdala damage on emotion perception and the nature and time-course of spatial attentional bias towards fearful faces. We investigated SF, a 14-year-old with selective bilateral amygdala damage due to Urbach–Wiethe disease (UWD), and ten healthy controls. Participants completed a fear sensitivity questionnaire, facial expression classification task, and dot-probe task with fearful or neutral faces for spatial cueing. Three cue durations were used to assess the time-course of attentional bias. SF expressed significantly lower fear sensitivity, and showed a selective impairment in classifying fearful facial expressions. Despite this impairment in fear recognition, very brief (100 msec) fearful cues could orient SF's spatial attention. In healthy controls, the attentional bias emerged later and persisted longer. SF's attentional bias was due solely to facilitated engagement to fear, while controls showed the typical phenomenon of difficulty in disengaging from fear. Our study is the first to demonstrate the separable effects of amygdala damage on engagement and disengagement of spatial attention. The findings indicate that multiple mechanisms contribute in biasing attention towards fear, which vary in their timing and dependence on amygdala integrity. It seems that the amygdala is not essential for rapid attention to emotion, but probably has a role in assessment of biological relevance.
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spelling pubmed-49627762016-08-03 Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage Pishnamazi, Morteza Tafakhori, Abbas Loloee, Sogol Modabbernia, Amirhossein Aghamollaii, Vajiheh Bahrami, Bahador Winston, Joel S. Cortex Research Report The amygdala is believed to play a major role in orienting attention towards threat-related stimuli. However, behavioral studies on amygdala-damaged patients have given inconsistent results—variously reporting decreased, persisted, and increased attention towards threat. Here we aimed to characterize the impact of developmental amygdala damage on emotion perception and the nature and time-course of spatial attentional bias towards fearful faces. We investigated SF, a 14-year-old with selective bilateral amygdala damage due to Urbach–Wiethe disease (UWD), and ten healthy controls. Participants completed a fear sensitivity questionnaire, facial expression classification task, and dot-probe task with fearful or neutral faces for spatial cueing. Three cue durations were used to assess the time-course of attentional bias. SF expressed significantly lower fear sensitivity, and showed a selective impairment in classifying fearful facial expressions. Despite this impairment in fear recognition, very brief (100 msec) fearful cues could orient SF's spatial attention. In healthy controls, the attentional bias emerged later and persisted longer. SF's attentional bias was due solely to facilitated engagement to fear, while controls showed the typical phenomenon of difficulty in disengaging from fear. Our study is the first to demonstrate the separable effects of amygdala damage on engagement and disengagement of spatial attention. The findings indicate that multiple mechanisms contribute in biasing attention towards fear, which vary in their timing and dependence on amygdala integrity. It seems that the amygdala is not essential for rapid attention to emotion, but probably has a role in assessment of biological relevance. Masson 2016-08 /pmc/articles/PMC4962776/ /pubmed/27173975 http://dx.doi.org/10.1016/j.cortex.2016.04.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Report
Pishnamazi, Morteza
Tafakhori, Abbas
Loloee, Sogol
Modabbernia, Amirhossein
Aghamollaii, Vajiheh
Bahrami, Bahador
Winston, Joel S.
Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title_full Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title_fullStr Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title_full_unstemmed Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title_short Attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
title_sort attentional bias towards and away from fearful faces is modulated by developmental amygdala damage
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962776/
https://www.ncbi.nlm.nih.gov/pubmed/27173975
http://dx.doi.org/10.1016/j.cortex.2016.04.012
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