Celiac disease diagnosis from videocapsule endoscopy images with residual learning and deep feature extraction

•A novel block wise feature recalibrate module merged into CNN-based networks for CD recognition.•Squeeze and excitation block with channel recalibration is firstly applied to adaptively recalibrate the feature of CD image.•The combination of ResNet50 with the SVM classifier can be useful to measure...

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Veröffentlicht in:Computer methods and programs in biomedicine 2020-04, Vol.187, p.105236-105236, Article 105236
Hauptverfasser: Wang, Xinle, Qian, Haiyang, Ciaccio, Edward J., Lewis, Suzanne K., Bhagat, Govind, Green, Peter H., Xu, Shenghao, Huang, Liang, Gao, Rongke, Liu, Yu
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container_title Computer methods and programs in biomedicine
container_volume 187
creator Wang, Xinle
Qian, Haiyang
Ciaccio, Edward J.
Lewis, Suzanne K.
Bhagat, Govind
Green, Peter H.
Xu, Shenghao
Huang, Liang
Gao, Rongke
Liu, Yu
description •A novel block wise feature recalibrate module merged into CNN-based networks for CD recognition.•Squeeze and excitation block with channel recalibration is firstly applied to adaptively recalibrate the feature of CD image.•The combination of ResNet50 with the SVM classifier can be useful to measure discriminative and subtle villous atrophy in CD. Videocapsule endoscopy (VCE) is a relatively new technique for evaluating the presence of villous atrophy in celiac disease patients. The diagnostic analysis of video frames is currently time-consuming and tedious. Recently, computer-aided diagnosis (CAD) systems have become an attractive research area for diagnosing celiac disease. However, the images captured from VCE are susceptible to alterations in light illumination, rotation direction, and intestinal secretions. Moreover, textural features of the mucosal villi obtained by VCE are difficult to characterize and extract. This work aims to find a novel deep learning feature learning module to assist in the diagnosis of celiac disease. In this manuscript, we propose a novel deep learning recalibration module which shows significant gain in diagnosing celiac disease. In this recalibration module, the block-wise recalibration component is newly employed to capture the most salient feature in the local channel feature map. This learning module was embedded into ResNet50, Inception-v3 to diagnose celiac disease using a 10-time 10-fold cross-validation based upon analysis of VCE images. In addition, we employed model weights to extract feature points from training and test samples before the last fully connected layer, and then input to a support vector machine (SVM), k-nearest neighbor (KNN), and linear discriminant analysis (LDA) for differentiating celiac disease images from heathy controls. Overall, the accuracy, sensitivity and specificity of the 10-time 10-fold cross-validation were 95.94%, 97.20% and 95.63%, respectively. A novel deep learning recalibration module, with global response and local salient factors is proposed, and it has a high potential for utilizing deep learning networks to diagnose celiac disease using VCE images. [Display omitted]
doi_str_mv 10.1016/j.cmpb.2019.105236
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Videocapsule endoscopy (VCE) is a relatively new technique for evaluating the presence of villous atrophy in celiac disease patients. The diagnostic analysis of video frames is currently time-consuming and tedious. Recently, computer-aided diagnosis (CAD) systems have become an attractive research area for diagnosing celiac disease. However, the images captured from VCE are susceptible to alterations in light illumination, rotation direction, and intestinal secretions. Moreover, textural features of the mucosal villi obtained by VCE are difficult to characterize and extract. This work aims to find a novel deep learning feature learning module to assist in the diagnosis of celiac disease. In this manuscript, we propose a novel deep learning recalibration module which shows significant gain in diagnosing celiac disease. In this recalibration module, the block-wise recalibration component is newly employed to capture the most salient feature in the local channel feature map. This learning module was embedded into ResNet50, Inception-v3 to diagnose celiac disease using a 10-time 10-fold cross-validation based upon analysis of VCE images. In addition, we employed model weights to extract feature points from training and test samples before the last fully connected layer, and then input to a support vector machine (SVM), k-nearest neighbor (KNN), and linear discriminant analysis (LDA) for differentiating celiac disease images from heathy controls. Overall, the accuracy, sensitivity and specificity of the 10-time 10-fold cross-validation were 95.94%, 97.20% and 95.63%, respectively. A novel deep learning recalibration module, with global response and local salient factors is proposed, and it has a high potential for utilizing deep learning networks to diagnose celiac disease using VCE images. 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Videocapsule endoscopy (VCE) is a relatively new technique for evaluating the presence of villous atrophy in celiac disease patients. The diagnostic analysis of video frames is currently time-consuming and tedious. Recently, computer-aided diagnosis (CAD) systems have become an attractive research area for diagnosing celiac disease. However, the images captured from VCE are susceptible to alterations in light illumination, rotation direction, and intestinal secretions. Moreover, textural features of the mucosal villi obtained by VCE are difficult to characterize and extract. This work aims to find a novel deep learning feature learning module to assist in the diagnosis of celiac disease. In this manuscript, we propose a novel deep learning recalibration module which shows significant gain in diagnosing celiac disease. In this recalibration module, the block-wise recalibration component is newly employed to capture the most salient feature in the local channel feature map. This learning module was embedded into ResNet50, Inception-v3 to diagnose celiac disease using a 10-time 10-fold cross-validation based upon analysis of VCE images. In addition, we employed model weights to extract feature points from training and test samples before the last fully connected layer, and then input to a support vector machine (SVM), k-nearest neighbor (KNN), and linear discriminant analysis (LDA) for differentiating celiac disease images from heathy controls. Overall, the accuracy, sensitivity and specificity of the 10-time 10-fold cross-validation were 95.94%, 97.20% and 95.63%, respectively. A novel deep learning recalibration module, with global response and local salient factors is proposed, and it has a high potential for utilizing deep learning networks to diagnose celiac disease using VCE images. [Display omitted]</description><subject>Algorithms</subject><subject>Block-wise channel squeeze and excitation component</subject><subject>Calibration</subject><subject>Capsule Endoscopy</subject><subject>Celiac disease</subject><subject>Celiac Disease - diagnostic imaging</subject><subject>Deep Learning</subject><subject>Diagnosis, Computer-Assisted - methods</subject><subject>Discriminant Analysis</subject><subject>Endoscopy</subject><subject>Humans</subject><subject>Image Interpretation, Computer-Assisted - methods</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Intestinal Mucosa - diagnostic imaging</subject><subject>Light</subject><subject>Linear Models</subject><subject>Machine Learning</subject><subject>Reproducibility of Results</subject><subject>Residual network</subject><subject>Sensitivity and Specificity</subject><subject>Support Vector Machine</subject><subject>Videocapsule endoscopy</subject><issn>0169-2607</issn><issn>1872-7565</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1P4zAQhi3EihaWP8AB-cglxXZqJ5W4oIpdkCpx2T1bjj0prhI7eBI-_v26apcjp5FGz_tq5iHkirMFZ1zd7ha2H5qFYHyVF1KU6oTMeV2JopJKnpJ5hlaFUKyakXPEHWNMSKnOyKzkVa2WUsxJWEPnjaXOIxiEPM02RPRI2xR7-uYdRGsGnDqgEFxEG4dP6nuzBaTvfnyhCdC7yXS0A5OCD1tqgqMOYKAtmHFKOfgxJmNHH8NP8qM1HcLlcV6Qv78e_qwfi83z76f1_aawSybHQlXMGpUPd8IxtywVlLx2ULemMbWV3Iq2qUA415QV46KRQq6c4k1dA29FK8oLcnPoHVJ8nQBH3Xu00HUmQJxQi1IwVdac84yKA2pTREzQ6iHl_9Kn5kzvPeud3nvWe8_64DmHro_9U9OD-4r8F5uBuwMA-cs3D0mj9RAsOJ_AjtpF_13_P8TdkKw</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Wang, Xinle</creator><creator>Qian, Haiyang</creator><creator>Ciaccio, Edward J.</creator><creator>Lewis, Suzanne K.</creator><creator>Bhagat, Govind</creator><creator>Green, Peter H.</creator><creator>Xu, Shenghao</creator><creator>Huang, Liang</creator><creator>Gao, Rongke</creator><creator>Liu, Yu</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202004</creationdate><title>Celiac disease diagnosis from videocapsule endoscopy images with residual learning and deep feature extraction</title><author>Wang, Xinle ; 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Videocapsule endoscopy (VCE) is a relatively new technique for evaluating the presence of villous atrophy in celiac disease patients. The diagnostic analysis of video frames is currently time-consuming and tedious. Recently, computer-aided diagnosis (CAD) systems have become an attractive research area for diagnosing celiac disease. However, the images captured from VCE are susceptible to alterations in light illumination, rotation direction, and intestinal secretions. Moreover, textural features of the mucosal villi obtained by VCE are difficult to characterize and extract. This work aims to find a novel deep learning feature learning module to assist in the diagnosis of celiac disease. In this manuscript, we propose a novel deep learning recalibration module which shows significant gain in diagnosing celiac disease. In this recalibration module, the block-wise recalibration component is newly employed to capture the most salient feature in the local channel feature map. This learning module was embedded into ResNet50, Inception-v3 to diagnose celiac disease using a 10-time 10-fold cross-validation based upon analysis of VCE images. In addition, we employed model weights to extract feature points from training and test samples before the last fully connected layer, and then input to a support vector machine (SVM), k-nearest neighbor (KNN), and linear discriminant analysis (LDA) for differentiating celiac disease images from heathy controls. Overall, the accuracy, sensitivity and specificity of the 10-time 10-fold cross-validation were 95.94%, 97.20% and 95.63%, respectively. A novel deep learning recalibration module, with global response and local salient factors is proposed, and it has a high potential for utilizing deep learning networks to diagnose celiac disease using VCE images. [Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>31786452</pmid><doi>10.1016/j.cmpb.2019.105236</doi><tpages>1</tpages></addata></record>
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subjects Algorithms
Block-wise channel squeeze and excitation component
Calibration
Capsule Endoscopy
Celiac disease
Celiac Disease - diagnostic imaging
Deep Learning
Diagnosis, Computer-Assisted - methods
Discriminant Analysis
Endoscopy
Humans
Image Interpretation, Computer-Assisted - methods
Image Processing, Computer-Assisted - methods
Intestinal Mucosa - diagnostic imaging
Light
Linear Models
Machine Learning
Reproducibility of Results
Residual network
Sensitivity and Specificity
Support Vector Machine
Videocapsule endoscopy
title Celiac disease diagnosis from videocapsule endoscopy images with residual learning and deep feature extraction
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