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Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder

BACKGROUND: New evidence suggests that the centromedial amygdala (CMA) and the basolateral amygdala (BLA) play different roles in threat processing. Our study aimed to investigate the effects of trauma and post‐traumatic stress disorder (PTSD) on the functional connectivity (FC) of the amygdala and...

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Autores principales: Liu, Tao, Ke, Jun, Qi, Rongfeng, Zhang, Li, Zhang, Zhiqiang, Xu, Qiang, Zhong, Yuan, Lu, Guangming, Chen, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821579/
https://www.ncbi.nlm.nih.gov/pubmed/33205889
http://dx.doi.org/10.1002/brb3.1952
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author Liu, Tao
Ke, Jun
Qi, Rongfeng
Zhang, Li
Zhang, Zhiqiang
Xu, Qiang
Zhong, Yuan
Lu, Guangming
Chen, Feng
author_facet Liu, Tao
Ke, Jun
Qi, Rongfeng
Zhang, Li
Zhang, Zhiqiang
Xu, Qiang
Zhong, Yuan
Lu, Guangming
Chen, Feng
author_sort Liu, Tao
collection PubMed
description BACKGROUND: New evidence suggests that the centromedial amygdala (CMA) and the basolateral amygdala (BLA) play different roles in threat processing. Our study aimed to investigate the effects of trauma and post‐traumatic stress disorder (PTSD) on the functional connectivity (FC) of the amygdala and its subregions. METHODS: Twenty‐seven patients with typhoon‐related PTSD, 33 trauma‐exposed controls (TEC), and 30 healthy controls (HC) were scanned with a 3‐Tesla magnetic resonance imaging scanner. The FCs of the BLA, the CMA, and the amygdala as a whole were examined using a seed‐based approach, and then, the analysis of variance was used to compare the groups. RESULTS: We demonstrated that the BLA had a stronger connectivity with the prefrontal cortices (PFCs) and angular gyrus in the PTSD group than in the TEC group. Additionally, compared with the PTSD and the HC groups, the TEC group exhibited decreased and increased BLA FC with the ventromedial PFC and postcentral gyrus (PoCG), respectively. Furthermore, the PTSD group showed abnormal FC between the salience network and default‐mode network, as well as the executive control network. Compared with the HC group, the TEC group and the PTSD group both showed decreased BLA FC with the superior temporal gyrus (STG). Finally, the FCs between the bilateral amygdala (as a whole) and the vmPFC, and between the BLA and the vmPFC have a negative correlation with the severity of PTSD. CONCLUSIONS: Decreased BLA‐vmPFC FC and increased BLA‐PoCG FC may reflect PTSD resilience factors. Trauma leads to decreased connectivity between the BLA and the STG, which could be further aggravated by PTSD.
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spelling pubmed-78215792021-01-29 Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder Liu, Tao Ke, Jun Qi, Rongfeng Zhang, Li Zhang, Zhiqiang Xu, Qiang Zhong, Yuan Lu, Guangming Chen, Feng Brain Behav Original Research BACKGROUND: New evidence suggests that the centromedial amygdala (CMA) and the basolateral amygdala (BLA) play different roles in threat processing. Our study aimed to investigate the effects of trauma and post‐traumatic stress disorder (PTSD) on the functional connectivity (FC) of the amygdala and its subregions. METHODS: Twenty‐seven patients with typhoon‐related PTSD, 33 trauma‐exposed controls (TEC), and 30 healthy controls (HC) were scanned with a 3‐Tesla magnetic resonance imaging scanner. The FCs of the BLA, the CMA, and the amygdala as a whole were examined using a seed‐based approach, and then, the analysis of variance was used to compare the groups. RESULTS: We demonstrated that the BLA had a stronger connectivity with the prefrontal cortices (PFCs) and angular gyrus in the PTSD group than in the TEC group. Additionally, compared with the PTSD and the HC groups, the TEC group exhibited decreased and increased BLA FC with the ventromedial PFC and postcentral gyrus (PoCG), respectively. Furthermore, the PTSD group showed abnormal FC between the salience network and default‐mode network, as well as the executive control network. Compared with the HC group, the TEC group and the PTSD group both showed decreased BLA FC with the superior temporal gyrus (STG). Finally, the FCs between the bilateral amygdala (as a whole) and the vmPFC, and between the BLA and the vmPFC have a negative correlation with the severity of PTSD. CONCLUSIONS: Decreased BLA‐vmPFC FC and increased BLA‐PoCG FC may reflect PTSD resilience factors. Trauma leads to decreased connectivity between the BLA and the STG, which could be further aggravated by PTSD. John Wiley and Sons Inc. 2020-11-18 /pmc/articles/PMC7821579/ /pubmed/33205889 http://dx.doi.org/10.1002/brb3.1952 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals LLC This is an open access article under the terms of the http://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
Liu, Tao
Ke, Jun
Qi, Rongfeng
Zhang, Li
Zhang, Zhiqiang
Xu, Qiang
Zhong, Yuan
Lu, Guangming
Chen, Feng
Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title_full Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title_fullStr Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title_full_unstemmed Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title_short Altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
title_sort altered functional connectivity of the amygdala and its subregions in typhoon‐related post‐traumatic stress disorder
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821579/
https://www.ncbi.nlm.nih.gov/pubmed/33205889
http://dx.doi.org/10.1002/brb3.1952
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