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Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities
PURPOSE: Accurate segmentation (separating diseased portions of the lung from normal appearing lung) is a challenge in radiomic studies of non-neoplastic diseases, such as pulmonary tuberculosis (PTB). In this study, we developed a segmentation method, applicable to chest X-rays (CXR), that can elim...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Milan
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474191/ https://www.ncbi.nlm.nih.gov/pubmed/37474665 http://dx.doi.org/10.1007/s11547-023-01681-y |
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author | du Plessis, Tamarisk Ramkilawon, Gopika Rae, William Ian Duncombe Botha, Tanita Martinson, Neil Alexander Dixon, Sarah Alice Parry Kyme, Andre Sathekge, Mike Michael |
author_facet | du Plessis, Tamarisk Ramkilawon, Gopika Rae, William Ian Duncombe Botha, Tanita Martinson, Neil Alexander Dixon, Sarah Alice Parry Kyme, Andre Sathekge, Mike Michael |
author_sort | du Plessis, Tamarisk |
collection | PubMed |
description | PURPOSE: Accurate segmentation (separating diseased portions of the lung from normal appearing lung) is a challenge in radiomic studies of non-neoplastic diseases, such as pulmonary tuberculosis (PTB). In this study, we developed a segmentation method, applicable to chest X-rays (CXR), that can eliminate the need for precise disease delineation, and that is effective for constructing radiomic models for automatic PTB cavity classification. METHODS: This retrospective study used a dataset of 266 posteroanterior CXR of patients diagnosed with laboratory confirmed PTB. The lungs were segmented using a U-net-based in-house automatic segmentation model. A secondary segmentation was developed using a sliding window, superimposed on the primary lung segmentation. Pyradiomics was used for feature extraction from every window which increased the dimensionality of the data, but this allowed us to accurately capture the spread of the features across the lung. Two separate measures (standard-deviation and variance) were used to consolidate the features. Pearson’s correlation analysis (with a 0.8 cut-off value) was then applied for dimensionality reduction followed by the construction of Random Forest radiomic models. RESULTS: Two almost identical radiomic signatures consisting of 10 texture features each (9 were the same plus 1 other feature) were identified using the two separate consolidation measures. Two well performing random forest models were constructed from these signatures. The standard-deviation model (AUC = 0.9444 (95% CI, 0.8762; 0.9814)) performed marginally better than the variance model (AUC = 0.9288 (95% CI, 0.9046; 0.9843)). CONCLUSION: The introduction of the secondary sliding window segmentation on CXR could eliminate the need for disease delineation in pulmonary radiomic studies, and it could improve the accuracy of CXR reporting currently regaining prominence as a high-volume screening tool as the developed radiomic models correctly classify cavities from normal CXR. |
format | Online Article Text |
id | pubmed-10474191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Milan |
record_format | MEDLINE/PubMed |
spelling | pubmed-104741912023-09-03 Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities du Plessis, Tamarisk Ramkilawon, Gopika Rae, William Ian Duncombe Botha, Tanita Martinson, Neil Alexander Dixon, Sarah Alice Parry Kyme, Andre Sathekge, Mike Michael Radiol Med Chest Radiology PURPOSE: Accurate segmentation (separating diseased portions of the lung from normal appearing lung) is a challenge in radiomic studies of non-neoplastic diseases, such as pulmonary tuberculosis (PTB). In this study, we developed a segmentation method, applicable to chest X-rays (CXR), that can eliminate the need for precise disease delineation, and that is effective for constructing radiomic models for automatic PTB cavity classification. METHODS: This retrospective study used a dataset of 266 posteroanterior CXR of patients diagnosed with laboratory confirmed PTB. The lungs were segmented using a U-net-based in-house automatic segmentation model. A secondary segmentation was developed using a sliding window, superimposed on the primary lung segmentation. Pyradiomics was used for feature extraction from every window which increased the dimensionality of the data, but this allowed us to accurately capture the spread of the features across the lung. Two separate measures (standard-deviation and variance) were used to consolidate the features. Pearson’s correlation analysis (with a 0.8 cut-off value) was then applied for dimensionality reduction followed by the construction of Random Forest radiomic models. RESULTS: Two almost identical radiomic signatures consisting of 10 texture features each (9 were the same plus 1 other feature) were identified using the two separate consolidation measures. Two well performing random forest models were constructed from these signatures. The standard-deviation model (AUC = 0.9444 (95% CI, 0.8762; 0.9814)) performed marginally better than the variance model (AUC = 0.9288 (95% CI, 0.9046; 0.9843)). CONCLUSION: The introduction of the secondary sliding window segmentation on CXR could eliminate the need for disease delineation in pulmonary radiomic studies, and it could improve the accuracy of CXR reporting currently regaining prominence as a high-volume screening tool as the developed radiomic models correctly classify cavities from normal CXR. Springer Milan 2023-07-20 2023 /pmc/articles/PMC10474191/ /pubmed/37474665 http://dx.doi.org/10.1007/s11547-023-01681-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Chest Radiology du Plessis, Tamarisk Ramkilawon, Gopika Rae, William Ian Duncombe Botha, Tanita Martinson, Neil Alexander Dixon, Sarah Alice Parry Kyme, Andre Sathekge, Mike Michael Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title | Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title_full | Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title_fullStr | Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title_full_unstemmed | Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title_short | Introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
title_sort | introducing a secondary segmentation to construct a radiomics model for pulmonary tuberculosis cavities |
topic | Chest Radiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474191/ https://www.ncbi.nlm.nih.gov/pubmed/37474665 http://dx.doi.org/10.1007/s11547-023-01681-y |
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