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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...

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Autores principales: du Plessis, Tamarisk, Ramkilawon, Gopika, Rae, William Ian Duncombe, Botha, Tanita, Martinson, Neil Alexander, Dixon, Sarah Alice Parry, Kyme, Andre, Sathekge, Mike Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2023
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.
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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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