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Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study

PURPOSE: To explore the characteristics of the impairment of eye emotional recognition and related clinical factors in children with benign childhood epilepsy with centrotemporal spikes (BECT). METHODS: The Eye Basic Emotion Discrimination Task and Eye Complex Emotion Discrimination Task were used t...

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Autores principales: Wu, Lulu, Yang, Xinyu, Zhang, Kaili, Wang, Xiaocui, Yang, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213938/
https://www.ncbi.nlm.nih.gov/pubmed/33942564
http://dx.doi.org/10.1002/brb3.2154
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author Wu, Lulu
Yang, Xinyu
Zhang, Kaili
Wang, Xiaocui
Yang, Bin
author_facet Wu, Lulu
Yang, Xinyu
Zhang, Kaili
Wang, Xiaocui
Yang, Bin
author_sort Wu, Lulu
collection PubMed
description PURPOSE: To explore the characteristics of the impairment of eye emotional recognition and related clinical factors in children with benign childhood epilepsy with centrotemporal spikes (BECT). METHODS: The Eye Basic Emotion Discrimination Task and Eye Complex Emotion Discrimination Task were used to study emotion discrimination in 33 recently diagnosed BECT patients and 33 BECT patients after complete remission compared to respective age‐ and gender‐matched comparison participants. RESULTS: The scores for discrimination of sadness, fear, and disgust were significantly lower in the newly diagnosed BECT group than in the comparison group (p = .004, p = .019, and p = .044, respectively), while scores for recognizing happiness, anger, and surprise were not significantly different between the two groups (p = .248, p = .586, and p = .540, respectively). Our analysis revealed that the BECT onset age influences the scores for recognition of sadness, fear, and disgust (OR = 1.795, 95% CI: 1.097 to 2.936, p = .020; OR=1.846, 95% CI: 1.124 to 3.034, p = .016; OR = 1.851, 95% CI: 1.131–3.029, p = .014). After remission, the scores for discrimination of happiness, anger, sadness, fear, disgust, and surprise of the BECT group were not significantly different from the comparison group (p = .588, p = .765, p = .752, p = .984, p = .328, and p = .339, respectively). CONCLUSIONS: In our study, newly diagnosed BECT patients exhibited emotion discrimination dysfunction, mainly related to sadness, fear, and disgust, and this dysfunction was more severe the younger the age of onset was. However, after BECT remission, the ability to discriminate emotions returned to normal.
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spelling pubmed-82139382021-06-28 Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study Wu, Lulu Yang, Xinyu Zhang, Kaili Wang, Xiaocui Yang, Bin Brain Behav Original Research PURPOSE: To explore the characteristics of the impairment of eye emotional recognition and related clinical factors in children with benign childhood epilepsy with centrotemporal spikes (BECT). METHODS: The Eye Basic Emotion Discrimination Task and Eye Complex Emotion Discrimination Task were used to study emotion discrimination in 33 recently diagnosed BECT patients and 33 BECT patients after complete remission compared to respective age‐ and gender‐matched comparison participants. RESULTS: The scores for discrimination of sadness, fear, and disgust were significantly lower in the newly diagnosed BECT group than in the comparison group (p = .004, p = .019, and p = .044, respectively), while scores for recognizing happiness, anger, and surprise were not significantly different between the two groups (p = .248, p = .586, and p = .540, respectively). Our analysis revealed that the BECT onset age influences the scores for recognition of sadness, fear, and disgust (OR = 1.795, 95% CI: 1.097 to 2.936, p = .020; OR=1.846, 95% CI: 1.124 to 3.034, p = .016; OR = 1.851, 95% CI: 1.131–3.029, p = .014). After remission, the scores for discrimination of happiness, anger, sadness, fear, disgust, and surprise of the BECT group were not significantly different from the comparison group (p = .588, p = .765, p = .752, p = .984, p = .328, and p = .339, respectively). CONCLUSIONS: In our study, newly diagnosed BECT patients exhibited emotion discrimination dysfunction, mainly related to sadness, fear, and disgust, and this dysfunction was more severe the younger the age of onset was. However, after BECT remission, the ability to discriminate emotions returned to normal. John Wiley and Sons Inc. 2021-05-04 /pmc/articles/PMC8213938/ /pubmed/33942564 http://dx.doi.org/10.1002/brb3.2154 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Wu, Lulu
Yang, Xinyu
Zhang, Kaili
Wang, Xiaocui
Yang, Bin
Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title_full Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title_fullStr Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title_full_unstemmed Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title_short Impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: A neuropsychological study
title_sort impairment of eye emotion discrimination in benign childhood epilepsy with centrotemporal spikes: a neuropsychological study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8213938/
https://www.ncbi.nlm.nih.gov/pubmed/33942564
http://dx.doi.org/10.1002/brb3.2154
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