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Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning

An analysis of scar tissue is necessary to understand the pathological tissue conditions during or after the wound healing process. Hematoxylin and eosin (HE) staining has conventionally been applied to understand the morphology of scar tissue. However, the scar lesions cannot be analyzed from a who...

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Autores principales: Maknuna, Luluil, Kim, Hyeonsoo, Lee, Yeachan, Choi, Yoonjin, Kim, Hyunjung, Yi, Myunggi, Kang, Hyun Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871086/
https://www.ncbi.nlm.nih.gov/pubmed/35204623
http://dx.doi.org/10.3390/diagnostics12020534
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author Maknuna, Luluil
Kim, Hyeonsoo
Lee, Yeachan
Choi, Yoonjin
Kim, Hyunjung
Yi, Myunggi
Kang, Hyun Wook
author_facet Maknuna, Luluil
Kim, Hyeonsoo
Lee, Yeachan
Choi, Yoonjin
Kim, Hyunjung
Yi, Myunggi
Kang, Hyun Wook
author_sort Maknuna, Luluil
collection PubMed
description An analysis of scar tissue is necessary to understand the pathological tissue conditions during or after the wound healing process. Hematoxylin and eosin (HE) staining has conventionally been applied to understand the morphology of scar tissue. However, the scar lesions cannot be analyzed from a whole slide image. The current study aimed to develop a method for the rapid and automatic characterization of scar lesions in HE-stained scar tissues using a supervised and unsupervised learning algorithm. The supervised learning used a Mask region-based convolutional neural network (RCNN) to train a pattern from a data representation using MMDetection tools. The K-means algorithm characterized the HE-stained tissue and extracted the main features, such as the collagen density and directional variance of the collagen. The Mask RCNN model effectively predicted scar images using various backbone networks (e.g., ResNet50, ResNet101, ResNeSt50, and ResNeSt101) with high accuracy. The K-means clustering method successfully characterized the HE-stained tissue by separating the main features in terms of the collagen fiber and dermal mature components, namely, the glands, hair follicles, and nuclei. A quantitative analysis of the scar tissue in terms of the collagen density and directional variance of the collagen confirmed 50% differences between the normal and scar tissues. The proposed methods were utilized to characterize the pathological features of scar tissue for an objective histological analysis. The trained model is time-efficient when used for detection in place of a manual analysis. Machine learning-assisted analysis is expected to aid in understanding scar conditions, and to help establish an optimal treatment plan.
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spelling pubmed-88710862022-02-25 Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning Maknuna, Luluil Kim, Hyeonsoo Lee, Yeachan Choi, Yoonjin Kim, Hyunjung Yi, Myunggi Kang, Hyun Wook Diagnostics (Basel) Article An analysis of scar tissue is necessary to understand the pathological tissue conditions during or after the wound healing process. Hematoxylin and eosin (HE) staining has conventionally been applied to understand the morphology of scar tissue. However, the scar lesions cannot be analyzed from a whole slide image. The current study aimed to develop a method for the rapid and automatic characterization of scar lesions in HE-stained scar tissues using a supervised and unsupervised learning algorithm. The supervised learning used a Mask region-based convolutional neural network (RCNN) to train a pattern from a data representation using MMDetection tools. The K-means algorithm characterized the HE-stained tissue and extracted the main features, such as the collagen density and directional variance of the collagen. The Mask RCNN model effectively predicted scar images using various backbone networks (e.g., ResNet50, ResNet101, ResNeSt50, and ResNeSt101) with high accuracy. The K-means clustering method successfully characterized the HE-stained tissue by separating the main features in terms of the collagen fiber and dermal mature components, namely, the glands, hair follicles, and nuclei. A quantitative analysis of the scar tissue in terms of the collagen density and directional variance of the collagen confirmed 50% differences between the normal and scar tissues. The proposed methods were utilized to characterize the pathological features of scar tissue for an objective histological analysis. The trained model is time-efficient when used for detection in place of a manual analysis. Machine learning-assisted analysis is expected to aid in understanding scar conditions, and to help establish an optimal treatment plan. MDPI 2022-02-19 /pmc/articles/PMC8871086/ /pubmed/35204623 http://dx.doi.org/10.3390/diagnostics12020534 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Maknuna, Luluil
Kim, Hyeonsoo
Lee, Yeachan
Choi, Yoonjin
Kim, Hyunjung
Yi, Myunggi
Kang, Hyun Wook
Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title_full Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title_fullStr Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title_full_unstemmed Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title_short Automated Structural Analysis and Quantitative Characterization of Scar Tissue Using Machine Learning
title_sort automated structural analysis and quantitative characterization of scar tissue using machine learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8871086/
https://www.ncbi.nlm.nih.gov/pubmed/35204623
http://dx.doi.org/10.3390/diagnostics12020534
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