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Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms
Cognitive models assume that the incomplete integration of a traumatic experience into the autobiographical memory results in typical symptoms associated with post-traumatic stress disorder (PTSD) such as intrusive re-experiencing. Sleep supports the integration of new experiences into existing memo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907077/ https://www.ncbi.nlm.nih.gov/pubmed/33633161 http://dx.doi.org/10.1038/s41598-021-83838-1 |
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author | Wilhelm, Ines Azza, Yasmine Brennwald, Karin Ehrt-Schäfer, Yamina Seifritz, Erich Kleim, Birgit |
author_facet | Wilhelm, Ines Azza, Yasmine Brennwald, Karin Ehrt-Schäfer, Yamina Seifritz, Erich Kleim, Birgit |
author_sort | Wilhelm, Ines |
collection | PubMed |
description | Cognitive models assume that the incomplete integration of a traumatic experience into the autobiographical memory results in typical symptoms associated with post-traumatic stress disorder (PTSD) such as intrusive re-experiencing. Sleep supports the integration of new experiences into existing memory networks through memory consolidation. In fifty-six females, we investigated whether a 90-min daytime nap (n = 33) compared to a wake period (n = 23) after being exposed to an experimental trauma (i.e. a trauma film) prevents PTSD analogue symptoms. Intrusive memories were recorded for seven days using a diary, overall PTSD symptoms were assessed using the Impact of Event Scale (IES-R) and affective response to trauma cues were measured one week after experimental trauma. The two groups did not differ in any of the analogue PTSD symptoms. However, participants obtaining rapid eye movement (REM) sleep in the nap experienced less distressing intrusive memories. Moreover, the duration of REM sleep and slow wave activity was negatively correlated with analogue PTSD symptoms. Our findings suggest that even a short sleep period after experimental trauma can play a protective role in trauma memory formation but only if the nap contains REM sleep. Our data provide additional evidence for a critical role of REM sleep in PTSD development. |
format | Online Article Text |
id | pubmed-7907077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79070772021-02-26 Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms Wilhelm, Ines Azza, Yasmine Brennwald, Karin Ehrt-Schäfer, Yamina Seifritz, Erich Kleim, Birgit Sci Rep Article Cognitive models assume that the incomplete integration of a traumatic experience into the autobiographical memory results in typical symptoms associated with post-traumatic stress disorder (PTSD) such as intrusive re-experiencing. Sleep supports the integration of new experiences into existing memory networks through memory consolidation. In fifty-six females, we investigated whether a 90-min daytime nap (n = 33) compared to a wake period (n = 23) after being exposed to an experimental trauma (i.e. a trauma film) prevents PTSD analogue symptoms. Intrusive memories were recorded for seven days using a diary, overall PTSD symptoms were assessed using the Impact of Event Scale (IES-R) and affective response to trauma cues were measured one week after experimental trauma. The two groups did not differ in any of the analogue PTSD symptoms. However, participants obtaining rapid eye movement (REM) sleep in the nap experienced less distressing intrusive memories. Moreover, the duration of REM sleep and slow wave activity was negatively correlated with analogue PTSD symptoms. Our findings suggest that even a short sleep period after experimental trauma can play a protective role in trauma memory formation but only if the nap contains REM sleep. Our data provide additional evidence for a critical role of REM sleep in PTSD development. Nature Publishing Group UK 2021-02-25 /pmc/articles/PMC7907077/ /pubmed/33633161 http://dx.doi.org/10.1038/s41598-021-83838-1 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wilhelm, Ines Azza, Yasmine Brennwald, Karin Ehrt-Schäfer, Yamina Seifritz, Erich Kleim, Birgit Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title | Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title_full | Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title_fullStr | Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title_full_unstemmed | Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title_short | Investigating the effect of a nap following experimental trauma on analogue PTSD symptoms |
title_sort | investigating the effect of a nap following experimental trauma on analogue ptsd symptoms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907077/ https://www.ncbi.nlm.nih.gov/pubmed/33633161 http://dx.doi.org/10.1038/s41598-021-83838-1 |
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