Your browser doesn't support javascript.
loading
A Machine Learning Approach Enables Quantitative Measurement of Liver Histology and Disease Monitoring in NASH.
Taylor-Weiner, Amaro; Pokkalla, Harsha; Han, Ling; Jia, Catherine; Huss, Ryan; Chung, Chuhan; Elliott, Hunter; Glass, Benjamin; Pethia, Kishalve; Carrasco-Zevallos, Oscar; Shukla, Chinmay; Khettry, Urmila; Najarian, Robert; Taliano, Ross; Subramanian, G Mani; Myers, Robert P; Wapinski, Ilan; Khosla, Aditya; Resnick, Murray; Montalto, Michael C; Anstee, Quentin M; Wong, Vincent Wai-Sun; Trauner, Michael; Lawitz, Eric J; Harrison, Stephen A; Okanoue, Takeshi; Romero-Gomez, Manuel; Goodman, Zachary; Loomba, Rohit; Beck, Andrew H; Younossi, Zobair M.
Affiliation
  • Taylor-Weiner A; PathAI, Boston, MA.
  • Pokkalla H; PathAI, Boston, MA.
  • Han L; Gilead Sciences, Inc., Foster City, CA.
  • Jia C; Gilead Sciences, Inc., Foster City, CA.
  • Huss R; Gilead Sciences, Inc., Foster City, CA.
  • Chung C; Gilead Sciences, Inc., Foster City, CA.
  • Elliott H; PathAI, Boston, MA.
  • Glass B; PathAI, Boston, MA.
  • Pethia K; PathAI, Boston, MA.
  • Carrasco-Zevallos O; PathAI, Boston, MA.
  • Shukla C; PathAI, Boston, MA.
  • Khettry U; Lahey Hospital & Medical Center (Emeritus), Burlington, MA.
  • Najarian R; University Gastroenterology, Portsmouth, RI.
  • Taliano R; Warren Alpert Medical School of Brown University, Providence, RI.
  • Subramanian GM; Gilead Sciences, Inc., Foster City, CA.
  • Myers RP; Gilead Sciences, Inc., Foster City, CA.
  • Wapinski I; PathAI, Boston, MA.
  • Khosla A; PathAI, Boston, MA.
  • Resnick M; PathAI, Boston, MA.
  • Montalto MC; Warren Alpert Medical School of Brown University, Providence, RI.
  • Anstee QM; PathAI, Boston, MA.
  • Wong VW; Translational & Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
  • Trauner M; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
  • Lawitz EJ; Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna, Austria.
  • Harrison SA; Texas Liver Institute, UT Health San Antonio, San Antonio, TX.
  • Okanoue T; Pinnacle Clinical Research, San Antonio, TX.
  • Romero-Gomez M; Saiseikai Suita Hospital, Suita City, Japan.
  • Goodman Z; Hospital Universitario Virgen del Rocio, Sevilla, Spain.
  • Loomba R; Department of Medicine, Inova Fairfax Medical Campus, Falls Church, VA.
  • Beck AH; Betty and Guy Beatty Center for Integrated Research, Inova Health System, Falls Church, VA.
  • Younossi ZM; NAFLD Research Center, University of California at San Diego, La Jolla, CA.
Hepatology ; 74(1): 133-147, 2021 07.
Article in En | MEDLINE | ID: mdl-33570776
ABSTRACT
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Non-alcoholic Fatty Liver Disease / Deep Learning / Liver / Liver Cirrhosis Type of study: Clinical_trials / Guideline / Prognostic_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Hepatology Year: 2021 Document type: Article Affiliation country: Morocco

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Non-alcoholic Fatty Liver Disease / Deep Learning / Liver / Liver Cirrhosis Type of study: Clinical_trials / Guideline / Prognostic_studies Aspects: Patient_preference Limits: Humans Language: En Journal: Hepatology Year: 2021 Document type: Article Affiliation country: Morocco