Deep-Learning-Based Hepatic Ploidy Quantification Using H&E Histopathology Images

Author:

Wen Zhuoyu1ORCID,Lin Yu-Hsuan2ORCID,Wang Shidan1ORCID,Fujiwara Naoto3ORCID,Rong Ruichen1,Jin Kevin W.1ORCID,Yang Donghan M.1ORCID,Yao Bo1,Yang Shengjie1,Wang Tao14,Xie Yang156,Hoshida Yujin3ORCID,Zhu Hao27,Xiao Guanghua156

Affiliation:

1. Quantitative Biomedical Research Center, Department of Population and Data Sciences, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

2. Children’s Research Institute, Departments of Pediatrics and Internal Medicine, Center for Regenerative Science and Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

3. Division of Digestive and Liver Diseases, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

4. Center for the Genetics of Host Defense, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

5. Hamon Center for Regenerative Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

6. Department of Bioinformatics, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

7. Children’s Research Institute Mouse Genome Engineering Core, The University of Texas Southwestern Medical Center, Dallas, TX 75390, USA

Abstract

Polyploidy, the duplication of the entire genome within a single cell, is a significant characteristic of cells in many tissues, including the liver. The quantification of hepatic ploidy typically relies on flow cytometry and immunofluorescence (IF) imaging, which are not widely available in clinical settings due to high financial and time costs. To improve accessibility for clinical samples, we developed a computational algorithm to quantify hepatic ploidy using hematoxylin-eosin (H&E) histopathology images, which are commonly obtained during routine clinical practice. Our algorithm uses a deep learning model to first segment and classify different types of cell nuclei in H&E images. It then determines cellular ploidy based on the relative distance between identified hepatocyte nuclei and determines nuclear ploidy using a fitted Gaussian mixture model. The algorithm can establish the total number of hepatocytes and their detailed ploidy information in a region of interest (ROI) on H&E images. This is the first successful attempt to automate ploidy analysis on H&E images. Our algorithm is expected to serve as an important tool for studying the role of polyploidy in human liver disease.

Funder

NIH

Cancer Prevention and Research Institute of Texas

the European Commission

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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