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Automatic detection of major depressive disorder using electrodermal activity
Major depressive disorder (MDD) is a common psychiatric disorder and the leading cause of disability worldwide. However, current methods used to diagnose depression mainly rely on clinical interviews and self-reported scales of depressive symptoms, which lack objectivity and efficiency. To address t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242826/ https://www.ncbi.nlm.nih.gov/pubmed/30451895 http://dx.doi.org/10.1038/s41598-018-35147-3 |
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author | Kim, Ah Young Jang, Eun Hye Kim, Seunghwan Choi, Kwan Woo Jeon, Hong Jin Yu, Han Young Byun, Sangwon |
author_facet | Kim, Ah Young Jang, Eun Hye Kim, Seunghwan Choi, Kwan Woo Jeon, Hong Jin Yu, Han Young Byun, Sangwon |
author_sort | Kim, Ah Young |
collection | PubMed |
description | Major depressive disorder (MDD) is a common psychiatric disorder and the leading cause of disability worldwide. However, current methods used to diagnose depression mainly rely on clinical interviews and self-reported scales of depressive symptoms, which lack objectivity and efficiency. To address this challenge, we present a machine learning approach to screen for MDD using electrodermal activity (EDA). Participants included 30 patients with MDD and 37 healthy controls. Their EDA was measured during five experimental phases consisted of baseline, mental arithmetic task, recovery from the stress task, relaxation task, and recovery from the relaxation task, which elicited multiple alterations in autonomic activity. Selected EDA features were extracted from each phase, and differential EDA features between two distinct phases were evaluated. By using these features as input data and performing feature selection with SVM-RFE, 74% accuracy, 74% sensitivity, and 71% specificity could be achieved by our decision tree classifier. The most relevant features selected by SVM-RFE included differential EDA features and features from the stress and relaxation tasks. These findings suggest that automatic detection of depression based on EDA features is feasible and that monitoring changes in physiological signal when a subject is experiencing autonomic arousal and recovery may enhance discrimination power. |
format | Online Article Text |
id | pubmed-6242826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62428262018-11-27 Automatic detection of major depressive disorder using electrodermal activity Kim, Ah Young Jang, Eun Hye Kim, Seunghwan Choi, Kwan Woo Jeon, Hong Jin Yu, Han Young Byun, Sangwon Sci Rep Article Major depressive disorder (MDD) is a common psychiatric disorder and the leading cause of disability worldwide. However, current methods used to diagnose depression mainly rely on clinical interviews and self-reported scales of depressive symptoms, which lack objectivity and efficiency. To address this challenge, we present a machine learning approach to screen for MDD using electrodermal activity (EDA). Participants included 30 patients with MDD and 37 healthy controls. Their EDA was measured during five experimental phases consisted of baseline, mental arithmetic task, recovery from the stress task, relaxation task, and recovery from the relaxation task, which elicited multiple alterations in autonomic activity. Selected EDA features were extracted from each phase, and differential EDA features between two distinct phases were evaluated. By using these features as input data and performing feature selection with SVM-RFE, 74% accuracy, 74% sensitivity, and 71% specificity could be achieved by our decision tree classifier. The most relevant features selected by SVM-RFE included differential EDA features and features from the stress and relaxation tasks. These findings suggest that automatic detection of depression based on EDA features is feasible and that monitoring changes in physiological signal when a subject is experiencing autonomic arousal and recovery may enhance discrimination power. Nature Publishing Group UK 2018-11-19 /pmc/articles/PMC6242826/ /pubmed/30451895 http://dx.doi.org/10.1038/s41598-018-35147-3 Text en © The Author(s) 2018 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 Kim, Ah Young Jang, Eun Hye Kim, Seunghwan Choi, Kwan Woo Jeon, Hong Jin Yu, Han Young Byun, Sangwon Automatic detection of major depressive disorder using electrodermal activity |
title | Automatic detection of major depressive disorder using electrodermal activity |
title_full | Automatic detection of major depressive disorder using electrodermal activity |
title_fullStr | Automatic detection of major depressive disorder using electrodermal activity |
title_full_unstemmed | Automatic detection of major depressive disorder using electrodermal activity |
title_short | Automatic detection of major depressive disorder using electrodermal activity |
title_sort | automatic detection of major depressive disorder using electrodermal activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6242826/ https://www.ncbi.nlm.nih.gov/pubmed/30451895 http://dx.doi.org/10.1038/s41598-018-35147-3 |
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