TY - GEN
T1 - Deep Learning for Predicting Pediatric Crohn's Disease Using Histopathological Imaging
AU - Sharma, Anahita H.
AU - Lawlor, Burke W.
AU - Wang, Jason Y.
AU - Sharma, Yash
AU - Sengupta, Saurav
AU - Fernandes, Philip
AU - Zulqarnain, Fatima
AU - May, Eve
AU - Syed, Sana
AU - Brown, Donald E.
N1 - Funding Information:
We thank INOVA and CCHMC for providing us with their medical imaging data sets, and the School of Data Science at UVA for facilitating this project. Research in this publication was supported in part by The National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health (award number K23DK117061-01A1), Litwin IBD Pioneers Award of the Crohn’s & Colitis Foundation, and the Virginia iTHRIV NIH-NCATS (award UL1TR003015).
Publisher Copyright:
© 2022 IEEE.
PY - 2022
Y1 - 2022
N2 - The current gold standard for Crohn's disease diagnosis involves the examination of biopsied tissue by a trained physician. However, endoscopic images and histological features are only evident when the appropriate biopsy site is chosen and the image is of high quality [1]. Thus, to prevent delayed diagnoses or reclassifications over time, additional tools to reinforce pathologists' diagnoses are necessary. Recent studies have showcased successful applications of deep learning for developing whole-slide classifications of digital histology images. In this study, we developed a patch-level image classification model for prediction of Crohn's disease using a convolutional neural network. This study obtained data from two different hospitals: INOVA and Cincinnati Children's Hospital Medical Center (CCHMC). When trained and validated on the same data set, our INOVA and CCHMC models achieved validation accuracies of 84.6 % and 93.9 %, respectively. However, the models performed poorly when trained on data from one site and tested on data from the other site. To investigate this issue, we built an additional patch-level model that was able to predict hospital source of the biopsy with 99 % accuracy. These results suggest the presence of site-specific artifacts which are detectable by machine learning models. We reduced the effects of these artifacts using color-normalization, image cropping, and other transformations, lowering site-predictive accuracy to 74%. Therefore, we suggest further works investigate reasons for inter-site biopsy differences such that site-generalizable, histopathological deep learning models can be developed.
AB - The current gold standard for Crohn's disease diagnosis involves the examination of biopsied tissue by a trained physician. However, endoscopic images and histological features are only evident when the appropriate biopsy site is chosen and the image is of high quality [1]. Thus, to prevent delayed diagnoses or reclassifications over time, additional tools to reinforce pathologists' diagnoses are necessary. Recent studies have showcased successful applications of deep learning for developing whole-slide classifications of digital histology images. In this study, we developed a patch-level image classification model for prediction of Crohn's disease using a convolutional neural network. This study obtained data from two different hospitals: INOVA and Cincinnati Children's Hospital Medical Center (CCHMC). When trained and validated on the same data set, our INOVA and CCHMC models achieved validation accuracies of 84.6 % and 93.9 %, respectively. However, the models performed poorly when trained on data from one site and tested on data from the other site. To investigate this issue, we built an additional patch-level model that was able to predict hospital source of the biopsy with 99 % accuracy. These results suggest the presence of site-specific artifacts which are detectable by machine learning models. We reduced the effects of these artifacts using color-normalization, image cropping, and other transformations, lowering site-predictive accuracy to 74%. Therefore, we suggest further works investigate reasons for inter-site biopsy differences such that site-generalizable, histopathological deep learning models can be developed.
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U2 - 10.1109/SIEDS55548.2022.9799299
DO - 10.1109/SIEDS55548.2022.9799299
M3 - Conference contribution
AN - SCOPUS:85134304898
T3 - 2022 Systems and Information Engineering Design Symposium, SIEDS 2022
SP - 122
EP - 127
BT - 2022 Systems and Information Engineering Design Symposium, SIEDS 2022
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2022 Systems and Information Engineering Design Symposium, SIEDS 2022
Y2 - 28 April 2022 through 29 April 2022
ER -