TY - JOUR
T1 - A Machine Learning Approach Enables Quantitative Measurement of Liver Histology and Disease Monitoring in NASH
AU - Taylor-Weiner, Amaro
AU - Pokkalla, Harsha
AU - Han, Ling
AU - Jia, Catherine
AU - Huss, Ryan
AU - Chung, Chuhan
AU - Elliott, Hunter
AU - Glass, Benjamin
AU - Pethia, Kishalve
AU - Carrasco-Zevallos, Oscar
AU - Shukla, Chinmay
AU - Khettry, Urmila
AU - Najarian, Robert
AU - Taliano, Ross
AU - Subramanian, G. Mani
AU - Myers, Robert P.
AU - Wapinski, Ilan
AU - Khosla, Aditya
AU - Resnick, Murray
AU - Montalto, Michael C.
AU - Anstee, Quentin M.
AU - Wong, Vincent Wai Sun
AU - Trauner, Michael
AU - Lawitz, Eric J.
AU - Harrison, Stephen A.
AU - Okanoue, Takeshi
AU - Romero-Gomez, Manuel
AU - Goodman, Zachary
AU - Loomba, Rohit
AU - Beck, Andrew H.
AU - Younossi, Zobair M.
N1 - Publisher Copyright:
© 2021 PathAI. Hepatology published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases.
PY - 2021/7
Y1 - 2021/7
N2 - Background and Aims: Manual histological assessment is currently the accepted standard for diagnosing and monitoring disease progression in NASH, but is limited by variability in interpretation and insensitivity to change. Thus, there is a critical need for improved tools to assess liver pathology in order to risk stratify NASH patients and monitor treatment response. Approach and Results: Here, we describe a machine learning (ML)-based approach to liver histology assessment, which accurately characterizes disease severity and heterogeneity, and sensitively quantifies treatment response in NASH. We use samples from three randomized controlled trials to build and then validate deep convolutional neural networks to measure key histological features in NASH, including steatosis, inflammation, hepatocellular ballooning, and fibrosis. The ML-based predictions showed strong correlations with expert pathologists and were prognostic of progression to cirrhosis and liver-related clinical events. We developed a heterogeneity-sensitive metric of fibrosis response, the Deep Learning Treatment Assessment Liver Fibrosis score, which measured antifibrotic treatment effects that went undetected by manual pathological staging and was concordant with histological disease progression. Conclusions: Our ML method has shown reproducibility and sensitivity and was prognostic for disease progression, demonstrating the power of ML to advance our understanding of disease heterogeneity in NASH, risk stratify affected patients, and facilitate the development of therapies.
AB - Background and Aims: Manual histological assessment is currently the accepted standard for diagnosing and monitoring disease progression in NASH, but is limited by variability in interpretation and insensitivity to change. Thus, there is a critical need for improved tools to assess liver pathology in order to risk stratify NASH patients and monitor treatment response. Approach and Results: Here, we describe a machine learning (ML)-based approach to liver histology assessment, which accurately characterizes disease severity and heterogeneity, and sensitively quantifies treatment response in NASH. We use samples from three randomized controlled trials to build and then validate deep convolutional neural networks to measure key histological features in NASH, including steatosis, inflammation, hepatocellular ballooning, and fibrosis. The ML-based predictions showed strong correlations with expert pathologists and were prognostic of progression to cirrhosis and liver-related clinical events. We developed a heterogeneity-sensitive metric of fibrosis response, the Deep Learning Treatment Assessment Liver Fibrosis score, which measured antifibrotic treatment effects that went undetected by manual pathological staging and was concordant with histological disease progression. Conclusions: Our ML method has shown reproducibility and sensitivity and was prognostic for disease progression, demonstrating the power of ML to advance our understanding of disease heterogeneity in NASH, risk stratify affected patients, and facilitate the development of therapies.
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U2 - 10.1002/hep.31750
DO - 10.1002/hep.31750
M3 - Article
C2 - 33570776
AN - SCOPUS:85106241900
SN - 0270-9139
VL - 74
SP - 133
EP - 147
JO - Hepatology
JF - Hepatology
IS - 1
ER -