Deep convolutional neural network-based algorithm for muscle biopsy diagnosis
Histopathologic evaluation of muscle biopsy samples is essential for classifying and diagnosing muscle diseases. However, the numbers of experienced specialists and pathologists are limited. Although new technologies such as artificial intelligence are expected to improve medical reach, their use wi...
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Veröffentlicht in: | Laboratory investigation 2022-03, Vol.102 (3), p.220-226 |
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creator | Kabeya, Yoshinori Okubo, Mariko Yonezawa, Sho Nakano, Hiroki Inoue, Michio Ogasawara, Masashi Saito, Yoshihiko Tanboon, Jantima Indrawati, Luh Ari Kumutpongpanich, Theerawat Chen, Yen-Lin Yoshioka, Wakako Hayashi, Shinichiro Iwamori, Toshiya Takeuchi, Yusuke Tokumasu, Reitaro Takano, Atsushi Matsuda, Fumihiko Nishino, Ichizo |
description | Histopathologic evaluation of muscle biopsy samples is essential for classifying and diagnosing muscle diseases. However, the numbers of experienced specialists and pathologists are limited. Although new technologies such as artificial intelligence are expected to improve medical reach, their use with rare diseases, such as muscle diseases, is challenging because of the limited availability of training datasets. To address this gap, we developed an algorithm based on deep convolutional neural networks (CNNs) and collected 4041 microscopic images of 1400 hematoxylin-and-eosin-stained pathology slides stored in the National Center of Neurology and Psychiatry for training CNNs. Our trained algorithm differentiated idiopathic inflammatory myopathies (mostly treatable) from hereditary muscle diseases (mostly non-treatable) with an area under the curve (AUC) of 0.996 and achieved better sensitivity and specificity than the diagnoses done by nine physicians under limited diseases and conditions. Furthermore, it successfully and accurately classified four subtypes of the idiopathic inflammatory myopathies with an average AUC of 0.958 and classified seven subtypes of hereditary muscle disease with an average AUC of 0.936. We also established a method to validate the similarity between the predictions made by the algorithm and the seven physicians using visualization technology and clarified the validity of the predictions. These results support the reliability of the algorithm and suggest that our algorithm has the potential to be used straightforwardly in a clinical setting.
The authors developed a deep convolutional neural network-based algorithm to support pathological muscle diagnosis. The algorithm differentiated idiopathic inflammatory myopathies and outperformed nine human physicians under limited diseases and conditions. These results suggest that the algorithm has the potential to be used directly in clinical settings. |
doi_str_mv | 10.1038/s41374-021-00647-w |
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The authors developed a deep convolutional neural network-based algorithm to support pathological muscle diagnosis. The algorithm differentiated idiopathic inflammatory myopathies and outperformed nine human physicians under limited diseases and conditions. These results suggest that the algorithm has the potential to be used directly in clinical settings.</description><identifier>ISSN: 0023-6837</identifier><identifier>EISSN: 1530-0307</identifier><identifier>DOI: 10.1038/s41374-021-00647-w</identifier><identifier>PMID: 34599274</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>14/63 ; 692/308 ; 692/699/375/374 ; Algorithms ; Animals ; Artificial intelligence ; Artificial neural networks ; Biopsy ; Deep Learning ; Diagnosis ; Diagnosis, Differential ; Humans ; Inflammation ; Laboratory Medicine ; Life Sciences ; Medicine ; Medicine & Public Health ; Muscles ; Muscles - pathology ; Muscular Diseases - diagnosis ; Muscular Diseases - pathology ; Myositis - diagnosis ; Myositis - pathology ; Neural networks ; Neural Networks, Computer ; Neurology ; New technology ; Pathology ; Physicians ; Psychiatry ; Rare diseases ; Reproducibility of Results ; Sensitivity and Specificity ; Training</subject><ispartof>Laboratory investigation, 2022-03, Vol.102 (3), p.220-226</ispartof><rights>2021 United States & Canadian Academy of Pathology</rights><rights>The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2021</rights><rights>2021. The Author(s), under exclusive licence to United States and Canadian Academy of Pathology.</rights><rights>The Author(s), under exclusive licence to United States and Canadian Academy of Pathology 2021.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-6e37b4e0e5bcf1b62b9e34fb757b4939432b4eae821babe47ae1588dcb7c5f553</citedby><cites>FETCH-LOGICAL-c572t-6e37b4e0e5bcf1b62b9e34fb757b4939432b4eae821babe47ae1588dcb7c5f553</cites><orcidid>0000-0001-9452-112X ; 0000-0003-1643-4797 ; 0000-0002-7564-4463</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34599274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03842220$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kabeya, Yoshinori</creatorcontrib><creatorcontrib>Okubo, Mariko</creatorcontrib><creatorcontrib>Yonezawa, Sho</creatorcontrib><creatorcontrib>Nakano, Hiroki</creatorcontrib><creatorcontrib>Inoue, Michio</creatorcontrib><creatorcontrib>Ogasawara, Masashi</creatorcontrib><creatorcontrib>Saito, Yoshihiko</creatorcontrib><creatorcontrib>Tanboon, Jantima</creatorcontrib><creatorcontrib>Indrawati, Luh Ari</creatorcontrib><creatorcontrib>Kumutpongpanich, Theerawat</creatorcontrib><creatorcontrib>Chen, Yen-Lin</creatorcontrib><creatorcontrib>Yoshioka, Wakako</creatorcontrib><creatorcontrib>Hayashi, Shinichiro</creatorcontrib><creatorcontrib>Iwamori, Toshiya</creatorcontrib><creatorcontrib>Takeuchi, Yusuke</creatorcontrib><creatorcontrib>Tokumasu, Reitaro</creatorcontrib><creatorcontrib>Takano, Atsushi</creatorcontrib><creatorcontrib>Matsuda, Fumihiko</creatorcontrib><creatorcontrib>Nishino, Ichizo</creatorcontrib><title>Deep convolutional neural network-based algorithm for muscle biopsy diagnosis</title><title>Laboratory investigation</title><addtitle>Lab Invest</addtitle><addtitle>Lab Invest</addtitle><description>Histopathologic evaluation of muscle biopsy samples is essential for classifying and diagnosing muscle diseases. However, the numbers of experienced specialists and pathologists are limited. Although new technologies such as artificial intelligence are expected to improve medical reach, their use with rare diseases, such as muscle diseases, is challenging because of the limited availability of training datasets. To address this gap, we developed an algorithm based on deep convolutional neural networks (CNNs) and collected 4041 microscopic images of 1400 hematoxylin-and-eosin-stained pathology slides stored in the National Center of Neurology and Psychiatry for training CNNs. Our trained algorithm differentiated idiopathic inflammatory myopathies (mostly treatable) from hereditary muscle diseases (mostly non-treatable) with an area under the curve (AUC) of 0.996 and achieved better sensitivity and specificity than the diagnoses done by nine physicians under limited diseases and conditions. Furthermore, it successfully and accurately classified four subtypes of the idiopathic inflammatory myopathies with an average AUC of 0.958 and classified seven subtypes of hereditary muscle disease with an average AUC of 0.936. We also established a method to validate the similarity between the predictions made by the algorithm and the seven physicians using visualization technology and clarified the validity of the predictions. These results support the reliability of the algorithm and suggest that our algorithm has the potential to be used straightforwardly in a clinical setting.
The authors developed a deep convolutional neural network-based algorithm to support pathological muscle diagnosis. The algorithm differentiated idiopathic inflammatory myopathies and outperformed nine human physicians under limited diseases and conditions. These results suggest that the algorithm has the potential to be used directly in clinical settings.</description><subject>14/63</subject><subject>692/308</subject><subject>692/699/375/374</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Artificial intelligence</subject><subject>Artificial neural networks</subject><subject>Biopsy</subject><subject>Deep Learning</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Laboratory Medicine</subject><subject>Life Sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Muscles</subject><subject>Muscles - pathology</subject><subject>Muscular Diseases - diagnosis</subject><subject>Muscular Diseases - pathology</subject><subject>Myositis - diagnosis</subject><subject>Myositis - pathology</subject><subject>Neural networks</subject><subject>Neural Networks, 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convolutional neural network-based algorithm for muscle biopsy diagnosis</title><author>Kabeya, Yoshinori ; Okubo, Mariko ; Yonezawa, Sho ; Nakano, Hiroki ; Inoue, Michio ; Ogasawara, Masashi ; Saito, Yoshihiko ; Tanboon, Jantima ; Indrawati, Luh Ari ; Kumutpongpanich, Theerawat ; Chen, Yen-Lin ; Yoshioka, Wakako ; Hayashi, Shinichiro ; Iwamori, Toshiya ; Takeuchi, Yusuke ; Tokumasu, Reitaro ; Takano, Atsushi ; Matsuda, Fumihiko ; Nishino, Ichizo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-6e37b4e0e5bcf1b62b9e34fb757b4939432b4eae821babe47ae1588dcb7c5f553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>14/63</topic><topic>692/308</topic><topic>692/699/375/374</topic><topic>Algorithms</topic><topic>Animals</topic><topic>Artificial intelligence</topic><topic>Artificial neural networks</topic><topic>Biopsy</topic><topic>Deep 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Invest</addtitle><date>2022-03-01</date><risdate>2022</risdate><volume>102</volume><issue>3</issue><spage>220</spage><epage>226</epage><pages>220-226</pages><issn>0023-6837</issn><eissn>1530-0307</eissn><abstract>Histopathologic evaluation of muscle biopsy samples is essential for classifying and diagnosing muscle diseases. However, the numbers of experienced specialists and pathologists are limited. Although new technologies such as artificial intelligence are expected to improve medical reach, their use with rare diseases, such as muscle diseases, is challenging because of the limited availability of training datasets. To address this gap, we developed an algorithm based on deep convolutional neural networks (CNNs) and collected 4041 microscopic images of 1400 hematoxylin-and-eosin-stained pathology slides stored in the National Center of Neurology and Psychiatry for training CNNs. Our trained algorithm differentiated idiopathic inflammatory myopathies (mostly treatable) from hereditary muscle diseases (mostly non-treatable) with an area under the curve (AUC) of 0.996 and achieved better sensitivity and specificity than the diagnoses done by nine physicians under limited diseases and conditions. Furthermore, it successfully and accurately classified four subtypes of the idiopathic inflammatory myopathies with an average AUC of 0.958 and classified seven subtypes of hereditary muscle disease with an average AUC of 0.936. We also established a method to validate the similarity between the predictions made by the algorithm and the seven physicians using visualization technology and clarified the validity of the predictions. These results support the reliability of the algorithm and suggest that our algorithm has the potential to be used straightforwardly in a clinical setting.
The authors developed a deep convolutional neural network-based algorithm to support pathological muscle diagnosis. The algorithm differentiated idiopathic inflammatory myopathies and outperformed nine human physicians under limited diseases and conditions. These results suggest that the algorithm has the potential to be used directly in clinical settings.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><pmid>34599274</pmid><doi>10.1038/s41374-021-00647-w</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9452-112X</orcidid><orcidid>https://orcid.org/0000-0003-1643-4797</orcidid><orcidid>https://orcid.org/0000-0002-7564-4463</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
subjects | 14/63 692/308 692/699/375/374 Algorithms Animals Artificial intelligence Artificial neural networks Biopsy Deep Learning Diagnosis Diagnosis, Differential Humans Inflammation Laboratory Medicine Life Sciences Medicine Medicine & Public Health Muscles Muscles - pathology Muscular Diseases - diagnosis Muscular Diseases - pathology Myositis - diagnosis Myositis - pathology Neural networks Neural Networks, Computer Neurology New technology Pathology Physicians Psychiatry Rare diseases Reproducibility of Results Sensitivity and Specificity Training |
title | Deep convolutional neural network-based algorithm for muscle biopsy diagnosis |
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