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Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features
BACKGROUND: The development of optimal classification criteria for specific mental disorders which share similar symptoms is an important issue for precise diagnosis. We investigated whether P300 features in both sensor-level and source-level could be effectively used to classify post-traumatic stre...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812119/ https://www.ncbi.nlm.nih.gov/pubmed/31627171 http://dx.doi.org/10.1016/j.nicl.2019.102001 |
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author | Shim, Miseon Jin, Min Jin Im, Chang-Hwan Lee, Seung-Hwan |
author_facet | Shim, Miseon Jin, Min Jin Im, Chang-Hwan Lee, Seung-Hwan |
author_sort | Shim, Miseon |
collection | PubMed |
description | BACKGROUND: The development of optimal classification criteria for specific mental disorders which share similar symptoms is an important issue for precise diagnosis. We investigated whether P300 features in both sensor-level and source-level could be effectively used to classify post-traumatic stress disorder (PTSD) and major depressive disorder (MDD). METHOD: EEG signals were recorded from fifty-one PTSD patients, 67 MDD patients, and 39 healthy controls (HCs) while performing an auditory oddball task. Amplitude and latency of P300 were evaluated, and the current source analysis of P300 components was conducted using sLORETA. Finally, we classified two groups using machine-learning methods with both sensor- and source-level features. Moreover, we checked the comorbidity effects using the same approaches (PTSD-mono diagnosis (PTSDm, n = 28) and PTSD-comorbid diagnosis (PTSDc, n = 23)). RESULTS: PTSD showed significantly reduced P300 amplitudes and prolonged latency compared to HCs and MDD. Moreover, PTSD showed significantly reduced source activities, and the source activities were significantly correlated with symptoms of depression and anxiety. Also, the best classification accuracy at each pair was as follows: 80.00% (PTSD-HCs), 67.92% (MDD-HCs), 70.34% (PTSD-MDD), 82.09% (PTSDm-HCs), 71.58% (PTSDm-MDD), 82.56% (PTSDc-HCs), and 76.67% (PTSDc- MDD). CONCLUSION: Since abnormal P300 reflects pathophysiological characteristics of PTSD, PTSD patients were well-discriminated from MDD and HCs when using P300 features. Thus, altered P300 characteristics in both sensor- and source-level may be useful biomarkers to diagnosis PTSD. |
format | Online Article Text |
id | pubmed-6812119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68121192019-10-30 Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features Shim, Miseon Jin, Min Jin Im, Chang-Hwan Lee, Seung-Hwan Neuroimage Clin Regular Article BACKGROUND: The development of optimal classification criteria for specific mental disorders which share similar symptoms is an important issue for precise diagnosis. We investigated whether P300 features in both sensor-level and source-level could be effectively used to classify post-traumatic stress disorder (PTSD) and major depressive disorder (MDD). METHOD: EEG signals were recorded from fifty-one PTSD patients, 67 MDD patients, and 39 healthy controls (HCs) while performing an auditory oddball task. Amplitude and latency of P300 were evaluated, and the current source analysis of P300 components was conducted using sLORETA. Finally, we classified two groups using machine-learning methods with both sensor- and source-level features. Moreover, we checked the comorbidity effects using the same approaches (PTSD-mono diagnosis (PTSDm, n = 28) and PTSD-comorbid diagnosis (PTSDc, n = 23)). RESULTS: PTSD showed significantly reduced P300 amplitudes and prolonged latency compared to HCs and MDD. Moreover, PTSD showed significantly reduced source activities, and the source activities were significantly correlated with symptoms of depression and anxiety. Also, the best classification accuracy at each pair was as follows: 80.00% (PTSD-HCs), 67.92% (MDD-HCs), 70.34% (PTSD-MDD), 82.09% (PTSDm-HCs), 71.58% (PTSDm-MDD), 82.56% (PTSDc-HCs), and 76.67% (PTSDc- MDD). CONCLUSION: Since abnormal P300 reflects pathophysiological characteristics of PTSD, PTSD patients were well-discriminated from MDD and HCs when using P300 features. Thus, altered P300 characteristics in both sensor- and source-level may be useful biomarkers to diagnosis PTSD. Elsevier 2019-09-05 /pmc/articles/PMC6812119/ /pubmed/31627171 http://dx.doi.org/10.1016/j.nicl.2019.102001 Text en © 2019 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Shim, Miseon Jin, Min Jin Im, Chang-Hwan Lee, Seung-Hwan Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title | Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title_full | Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title_fullStr | Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title_full_unstemmed | Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title_short | Machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using P300 features |
title_sort | machine-learning-based classification between post-traumatic stress disorder and major depressive disorder using p300 features |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812119/ https://www.ncbi.nlm.nih.gov/pubmed/31627171 http://dx.doi.org/10.1016/j.nicl.2019.102001 |
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