| Literature DB >> 33287662 |
Debra A Tokarz1, Thomas J Steinbach1, Avinash Lokhande2, Gargi Srivastava2, Rajesh Ugalmugle2, Caroll A Co3, Keith R Shockley4, Emily Singletary1, Mark F Cesta5, Heath C Thomas6, Vivian S Chen7, Kristen Hobbie8, Torrie A Crabbs1.
Abstract
Rodent progressive cardiomyopathy (PCM) encompasses a constellation of microscopic findings commonly seen as a spontaneous background change in rat and mouse hearts. Primary histologic features of PCM include varying degrees of cardiomyocyte degeneration/necrosis, mononuclear cell infiltration, and fibrosis. Mineralization can also occur. Cardiotoxicity may increase the incidence and severity of PCM, and toxicity-related morphologic changes can overlap with those of PCM. Consequently, sensitive and consistent detection and quantification of PCM features are needed to help differentiate spontaneous from test article-related findings. To address this, we developed a computer-assisted image analysis algorithm, facilitated by a fully convolutional network deep learning technique, to detect and quantify the microscopic features of PCM (degeneration/necrosis, fibrosis, mononuclear cell infiltration, mineralization) in rat heart histologic sections. The trained algorithm achieved high values for accuracy, intersection over union, and dice coefficient for each feature. Further, there was a strong positive correlation between the percentage area of the heart predicted to have PCM lesions by the algorithm and the median severity grade assigned by a panel of veterinary toxicologic pathologists following light microscopic evaluation. By providing objective and sensitive quantification of the microscopic features of PCM, deep learning algorithms could assist pathologists in discerning cardiotoxicity-associated changes.Entities:
Keywords: Sprague Dawley; artificial intelligence; cardiomyopathy; computer assisted image analysis; computer neural networks; deep learning; rat
Year: 2020 PMID: 33287662 DOI: 10.1177/0192623320972614
Source DB: PubMed Journal: Toxicol Pathol ISSN: 0192-6233 Impact factor: 1.902