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Assessment of dysplasia in bone marrow smear with convolutional neural network

In this study, we developed the world's first artificial intelligence (AI) system that assesses the dysplasia of blood cells on bone marrow smears and presents the result of AI prediction for one of the most representative dysplasia—decreased granules (DG). We photographed field images from the...

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Autores principales: Mori, Jinichi, Kaji, Shizuo, Kawai, Hiroki, Kida, Satoshi, Tsubokura, Masaharu, Fukatsu, Masahiko, Harada, Kayo, Noji, Hideyoshi, Ikezoe, Takayuki, Maeda, Tomoya, Matsuda, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477564/
https://www.ncbi.nlm.nih.gov/pubmed/32895431
http://dx.doi.org/10.1038/s41598-020-71752-x
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author Mori, Jinichi
Kaji, Shizuo
Kawai, Hiroki
Kida, Satoshi
Tsubokura, Masaharu
Fukatsu, Masahiko
Harada, Kayo
Noji, Hideyoshi
Ikezoe, Takayuki
Maeda, Tomoya
Matsuda, Akira
author_facet Mori, Jinichi
Kaji, Shizuo
Kawai, Hiroki
Kida, Satoshi
Tsubokura, Masaharu
Fukatsu, Masahiko
Harada, Kayo
Noji, Hideyoshi
Ikezoe, Takayuki
Maeda, Tomoya
Matsuda, Akira
author_sort Mori, Jinichi
collection PubMed
description In this study, we developed the world's first artificial intelligence (AI) system that assesses the dysplasia of blood cells on bone marrow smears and presents the result of AI prediction for one of the most representative dysplasia—decreased granules (DG). We photographed field images from the bone marrow smears from patients with myelodysplastic syndrome (MDS) or non-MDS diseases and cropped each cell using an originally developed cell detector. Two morphologists labelled each cell. The degree of dysplasia was evaluated on a four-point scale: 0–3 (e.g., neutrophil with severely decreased granules were labelled DG3). We then constructed the classifier from the dataset of labelled images. The detector and classifier were based on a deep neural network pre-trained with natural images. We obtained 1797 labelled images, and the morphologists determined 134 DGs (DG1: 46, DG2: 77, DG3: 11). Subsequently, we performed a five-fold cross-validation to evaluate the performance of the classifier. For DG1–3 labelled by morphologists, the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were 91.0%, 97.7%, 76.3%, 99.3%, and 97.2%, respectively. When DG1 was excluded in the process, the sensitivity, specificity, PPV, NPV, and accuracy were 85.2%, 98.9%, 80.6%, and 99.2% and 98.2%, respectively.
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spelling pubmed-74775642020-09-08 Assessment of dysplasia in bone marrow smear with convolutional neural network Mori, Jinichi Kaji, Shizuo Kawai, Hiroki Kida, Satoshi Tsubokura, Masaharu Fukatsu, Masahiko Harada, Kayo Noji, Hideyoshi Ikezoe, Takayuki Maeda, Tomoya Matsuda, Akira Sci Rep Article In this study, we developed the world's first artificial intelligence (AI) system that assesses the dysplasia of blood cells on bone marrow smears and presents the result of AI prediction for one of the most representative dysplasia—decreased granules (DG). We photographed field images from the bone marrow smears from patients with myelodysplastic syndrome (MDS) or non-MDS diseases and cropped each cell using an originally developed cell detector. Two morphologists labelled each cell. The degree of dysplasia was evaluated on a four-point scale: 0–3 (e.g., neutrophil with severely decreased granules were labelled DG3). We then constructed the classifier from the dataset of labelled images. The detector and classifier were based on a deep neural network pre-trained with natural images. We obtained 1797 labelled images, and the morphologists determined 134 DGs (DG1: 46, DG2: 77, DG3: 11). Subsequently, we performed a five-fold cross-validation to evaluate the performance of the classifier. For DG1–3 labelled by morphologists, the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy were 91.0%, 97.7%, 76.3%, 99.3%, and 97.2%, respectively. When DG1 was excluded in the process, the sensitivity, specificity, PPV, NPV, and accuracy were 85.2%, 98.9%, 80.6%, and 99.2% and 98.2%, respectively. Nature Publishing Group UK 2020-09-07 /pmc/articles/PMC7477564/ /pubmed/32895431 http://dx.doi.org/10.1038/s41598-020-71752-x Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mori, Jinichi
Kaji, Shizuo
Kawai, Hiroki
Kida, Satoshi
Tsubokura, Masaharu
Fukatsu, Masahiko
Harada, Kayo
Noji, Hideyoshi
Ikezoe, Takayuki
Maeda, Tomoya
Matsuda, Akira
Assessment of dysplasia in bone marrow smear with convolutional neural network
title Assessment of dysplasia in bone marrow smear with convolutional neural network
title_full Assessment of dysplasia in bone marrow smear with convolutional neural network
title_fullStr Assessment of dysplasia in bone marrow smear with convolutional neural network
title_full_unstemmed Assessment of dysplasia in bone marrow smear with convolutional neural network
title_short Assessment of dysplasia in bone marrow smear with convolutional neural network
title_sort assessment of dysplasia in bone marrow smear with convolutional neural network
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477564/
https://www.ncbi.nlm.nih.gov/pubmed/32895431
http://dx.doi.org/10.1038/s41598-020-71752-x
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