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Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study

Previous coronavirus pandemics were associated elevated post-traumatic stress symptoms (PTSS), but the self-report and neurological basis of PTSS in patients who survived coronavirus disease 2019 (COVID-19) are largely unknown. We conducted a two-session study to record PTSS in the COVID-19 survivor...

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Autores principales: Tu, Yiheng, Zhang, Yuqi, Li, Yu, Zhao, Qing, Bi, Yanzhi, Lu, Xuejing, Kong, Yazhuo, Wang, Li, Lu, Zhijie, Hu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290134/
https://www.ncbi.nlm.nih.gov/pubmed/34285348
http://dx.doi.org/10.1038/s41380-021-01223-w
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author Tu, Yiheng
Zhang, Yuqi
Li, Yu
Zhao, Qing
Bi, Yanzhi
Lu, Xuejing
Kong, Yazhuo
Wang, Li
Lu, Zhijie
Hu, Li
author_facet Tu, Yiheng
Zhang, Yuqi
Li, Yu
Zhao, Qing
Bi, Yanzhi
Lu, Xuejing
Kong, Yazhuo
Wang, Li
Lu, Zhijie
Hu, Li
author_sort Tu, Yiheng
collection PubMed
description Previous coronavirus pandemics were associated elevated post-traumatic stress symptoms (PTSS), but the self-report and neurological basis of PTSS in patients who survived coronavirus disease 2019 (COVID-19) are largely unknown. We conducted a two-session study to record PTSS in the COVID-19 survivors discharged from hospitals for a short (i.e., about 3 months, Session 1) to a medium period (i.e., about 6 months, Session 2), as well as brain imaging data in Session 2. The control groups were non-COVID-19 locals. Session 1 was completed for 126 COVID-19 survivors and 126 controls. Session 2 was completed for 47 COVID-19 survivors and 43 controls. The total score of post-traumatic stress disorder (PTSD) checklist for DSM-5 (PCL-5) score was significantly higher in COVID-19 survivors compared with controls in both sessions. The PCL-5 score in COVID-19 survivors was positively correlated with the duration after discharge (r = 0.27, p = 0.003 for Session 1), and increased by 20% from Session 1 to Session 2 for the survivors who participated both sessions. The increase was positively correlated with individual’s test-retest duration (r = 0.46, p = 0.03). Brain structural volume and functional activity in bilateral hippocampus and amygdala were significantly larger in COVID-19 survivors compared with controls. However, the volumes of the left hippocampus and amygdala were negatively correlated with the PCL-5 score for the COVID-19 survivors. Our study suggests that COVID-19 survivors might face possible PTSS deteriorations, and highlights the importance of monitoring mental wellness of COVID-19 survivors.
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spelling pubmed-82901342021-07-20 Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study Tu, Yiheng Zhang, Yuqi Li, Yu Zhao, Qing Bi, Yanzhi Lu, Xuejing Kong, Yazhuo Wang, Li Lu, Zhijie Hu, Li Mol Psychiatry Article Previous coronavirus pandemics were associated elevated post-traumatic stress symptoms (PTSS), but the self-report and neurological basis of PTSS in patients who survived coronavirus disease 2019 (COVID-19) are largely unknown. We conducted a two-session study to record PTSS in the COVID-19 survivors discharged from hospitals for a short (i.e., about 3 months, Session 1) to a medium period (i.e., about 6 months, Session 2), as well as brain imaging data in Session 2. The control groups were non-COVID-19 locals. Session 1 was completed for 126 COVID-19 survivors and 126 controls. Session 2 was completed for 47 COVID-19 survivors and 43 controls. The total score of post-traumatic stress disorder (PTSD) checklist for DSM-5 (PCL-5) score was significantly higher in COVID-19 survivors compared with controls in both sessions. The PCL-5 score in COVID-19 survivors was positively correlated with the duration after discharge (r = 0.27, p = 0.003 for Session 1), and increased by 20% from Session 1 to Session 2 for the survivors who participated both sessions. The increase was positively correlated with individual’s test-retest duration (r = 0.46, p = 0.03). Brain structural volume and functional activity in bilateral hippocampus and amygdala were significantly larger in COVID-19 survivors compared with controls. However, the volumes of the left hippocampus and amygdala were negatively correlated with the PCL-5 score for the COVID-19 survivors. Our study suggests that COVID-19 survivors might face possible PTSS deteriorations, and highlights the importance of monitoring mental wellness of COVID-19 survivors. Nature Publishing Group UK 2021-07-20 2021 /pmc/articles/PMC8290134/ /pubmed/34285348 http://dx.doi.org/10.1038/s41380-021-01223-w Text en © The Author(s), under exclusive licence to Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Tu, Yiheng
Zhang, Yuqi
Li, Yu
Zhao, Qing
Bi, Yanzhi
Lu, Xuejing
Kong, Yazhuo
Wang, Li
Lu, Zhijie
Hu, Li
Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title_full Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title_fullStr Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title_full_unstemmed Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title_short Post-traumatic stress symptoms in COVID-19 survivors: a self-report and brain imaging follow-up study
title_sort post-traumatic stress symptoms in covid-19 survivors: a self-report and brain imaging follow-up study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290134/
https://www.ncbi.nlm.nih.gov/pubmed/34285348
http://dx.doi.org/10.1038/s41380-021-01223-w
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