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Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder

Objective biomarkers of the presence and severity of posttraumatic stress disorder (PTSD) are elusive, yet badly needed. Electroencephalographic (EEG) coherence represents a promising approach to identifying and understanding brain biomarker activity in PTSD. Overnight polysomnography data containin...

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Autores principales: Modarres, Mo H., Opel, Ryan A., Weymann, Kristianna B., Lim, Miranda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414519/
https://www.ncbi.nlm.nih.gov/pubmed/30862872
http://dx.doi.org/10.1038/s41598-018-38102-4
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author Modarres, Mo H.
Opel, Ryan A.
Weymann, Kristianna B.
Lim, Miranda M.
author_facet Modarres, Mo H.
Opel, Ryan A.
Weymann, Kristianna B.
Lim, Miranda M.
author_sort Modarres, Mo H.
collection PubMed
description Objective biomarkers of the presence and severity of posttraumatic stress disorder (PTSD) are elusive, yet badly needed. Electroencephalographic (EEG) coherence represents a promising approach to identifying and understanding brain biomarker activity in PTSD. Overnight polysomnography data containing EEG across sleep and wake states was collected in n = 76 Veterans with and without PTSD from a single site under IRB approval. Brain coherence markers (BCM) were calculated from EEG signals using a novel approach to produce one index for PTSD diagnosis (PTSD(dx)), and another index for PTSD severity (PTSD(sev)). PTSD(dx) showed strong sensitivity to the presence of PTSD in the awake state, during non-rapid eye movement (NREM) stage N2 sleep, and in a hybrid BCM incorporating both awake and NREM sleep states. PTSD(sev) showed a strong correlation with PTSD symptom severity (using the PTSD Checklist 5, or PCL5 survey) in the awake state, during N2 sleep, and in a hybrid BCM incorporating both awake and NREM sleep states. Thus, sleep EEG-based brain coherence markers can be utilized as an objective means for determining the presence and severity of PTSD. This portable, inexpensive, and non-invasive tool holds promise for better understanding the physiological mechanisms underlying PTSD and for tracking objective responses to treatment.
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spelling pubmed-64145192019-03-14 Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder Modarres, Mo H. Opel, Ryan A. Weymann, Kristianna B. Lim, Miranda M. Sci Rep Article Objective biomarkers of the presence and severity of posttraumatic stress disorder (PTSD) are elusive, yet badly needed. Electroencephalographic (EEG) coherence represents a promising approach to identifying and understanding brain biomarker activity in PTSD. Overnight polysomnography data containing EEG across sleep and wake states was collected in n = 76 Veterans with and without PTSD from a single site under IRB approval. Brain coherence markers (BCM) were calculated from EEG signals using a novel approach to produce one index for PTSD diagnosis (PTSD(dx)), and another index for PTSD severity (PTSD(sev)). PTSD(dx) showed strong sensitivity to the presence of PTSD in the awake state, during non-rapid eye movement (NREM) stage N2 sleep, and in a hybrid BCM incorporating both awake and NREM sleep states. PTSD(sev) showed a strong correlation with PTSD symptom severity (using the PTSD Checklist 5, or PCL5 survey) in the awake state, during N2 sleep, and in a hybrid BCM incorporating both awake and NREM sleep states. Thus, sleep EEG-based brain coherence markers can be utilized as an objective means for determining the presence and severity of PTSD. This portable, inexpensive, and non-invasive tool holds promise for better understanding the physiological mechanisms underlying PTSD and for tracking objective responses to treatment. Nature Publishing Group UK 2019-03-12 /pmc/articles/PMC6414519/ /pubmed/30862872 http://dx.doi.org/10.1038/s41598-018-38102-4 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Modarres, Mo H.
Opel, Ryan A.
Weymann, Kristianna B.
Lim, Miranda M.
Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title_full Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title_fullStr Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title_full_unstemmed Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title_short Strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
title_sort strong correlation of novel sleep electroencephalography coherence markers with diagnosis and severity of posttraumatic stress disorder
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6414519/
https://www.ncbi.nlm.nih.gov/pubmed/30862872
http://dx.doi.org/10.1038/s41598-018-38102-4
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