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Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases
Background: Diagnosis of skin diseases is often challenging and computer-aided diagnostic tools are urgently needed to underpin decision making. Objective: To develop a convolutional neural network model to classify clinically relevant selected multiple-lesion skin diseases, this in accordance to th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536339/ https://www.ncbi.nlm.nih.gov/pubmed/33072786 http://dx.doi.org/10.3389/fmed.2020.574329 |
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author | Thomsen, Kenneth Christensen, Anja Liljedahl Iversen, Lars Lomholt, Hans Bredsted Winther, Ole |
author_facet | Thomsen, Kenneth Christensen, Anja Liljedahl Iversen, Lars Lomholt, Hans Bredsted Winther, Ole |
author_sort | Thomsen, Kenneth |
collection | PubMed |
description | Background: Diagnosis of skin diseases is often challenging and computer-aided diagnostic tools are urgently needed to underpin decision making. Objective: To develop a convolutional neural network model to classify clinically relevant selected multiple-lesion skin diseases, this in accordance to the STARD guidelines. Methods: This was an image-based retrospective study using multi-task learning for binary classification. A VGG-16 model was trained on 16,543 non-standardized images. Image data was distributed in training set (80%), validation set (10%), and test set (10%). All images were collected from a clinical database of a Danish population attending one dermatological department. Included was patients categorized with ICD-10 codes related to acne, rosacea, psoriasis, eczema, and cutaneous t-cell lymphoma. Results: Acne was distinguished from rosacea with a sensitivity of 85.42% CI 72.24–93.93% and a specificity of 89.53% CI 83.97–93.68%, cutaneous t-cell lymphoma was distinguished from eczema with a sensitivity of 74.29% CI 67.82–80.05% and a specificity of 84.09% CI 80.83–86.99%, and psoriasis from eczema with a sensitivity of 81.79% CI 78.51–84.76% and a specificity of 73.57% CI 69.76–77.13%. All results were based on the test set. Conclusion: The performance rates reported were equal or superior to those reported for general practitioners with dermatological training, indicating that computer-aided diagnostic models based on convolutional neural network may potentially be employed for diagnosing multiple-lesion skin diseases. |
format | Online Article Text |
id | pubmed-7536339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75363392020-10-16 Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases Thomsen, Kenneth Christensen, Anja Liljedahl Iversen, Lars Lomholt, Hans Bredsted Winther, Ole Front Med (Lausanne) Medicine Background: Diagnosis of skin diseases is often challenging and computer-aided diagnostic tools are urgently needed to underpin decision making. Objective: To develop a convolutional neural network model to classify clinically relevant selected multiple-lesion skin diseases, this in accordance to the STARD guidelines. Methods: This was an image-based retrospective study using multi-task learning for binary classification. A VGG-16 model was trained on 16,543 non-standardized images. Image data was distributed in training set (80%), validation set (10%), and test set (10%). All images were collected from a clinical database of a Danish population attending one dermatological department. Included was patients categorized with ICD-10 codes related to acne, rosacea, psoriasis, eczema, and cutaneous t-cell lymphoma. Results: Acne was distinguished from rosacea with a sensitivity of 85.42% CI 72.24–93.93% and a specificity of 89.53% CI 83.97–93.68%, cutaneous t-cell lymphoma was distinguished from eczema with a sensitivity of 74.29% CI 67.82–80.05% and a specificity of 84.09% CI 80.83–86.99%, and psoriasis from eczema with a sensitivity of 81.79% CI 78.51–84.76% and a specificity of 73.57% CI 69.76–77.13%. All results were based on the test set. Conclusion: The performance rates reported were equal or superior to those reported for general practitioners with dermatological training, indicating that computer-aided diagnostic models based on convolutional neural network may potentially be employed for diagnosing multiple-lesion skin diseases. Frontiers Media S.A. 2020-09-22 /pmc/articles/PMC7536339/ /pubmed/33072786 http://dx.doi.org/10.3389/fmed.2020.574329 Text en Copyright © 2020 Thomsen, Christensen, Iversen, Lomholt and Winther. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Thomsen, Kenneth Christensen, Anja Liljedahl Iversen, Lars Lomholt, Hans Bredsted Winther, Ole Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title | Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title_full | Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title_fullStr | Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title_full_unstemmed | Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title_short | Deep Learning for Diagnostic Binary Classification of Multiple-Lesion Skin Diseases |
title_sort | deep learning for diagnostic binary classification of multiple-lesion skin diseases |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536339/ https://www.ncbi.nlm.nih.gov/pubmed/33072786 http://dx.doi.org/10.3389/fmed.2020.574329 |
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