Deep learning models capture histological disease activity in Crohn's Disease and Ulcerative Colitis with high fidelity.

Artificial intelligence histology inflammatory bowel disease

Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
10 Oct 2023
Historique:
received: 11 05 2023
medline: 10 10 2023
pubmed: 10 10 2023
entrez: 9 10 2023
Statut: aheadofprint

Résumé

Histologic disease activity in Inflammatory Bowel Disease (IBD) is associated with clinical outcomes and is an important endpoint in drug development. We developed deep learning models for automating histological assessments in IBD. Histology images of intestinal mucosa from phase 2 and phase 3 clinical trials in Crohn's disease (CD) and Ulcerative Colitis (UC) were used to train artificial intelligence (AI) models to predict the Global Histology Activity Score (GHAS) for CD and Geboes histopathology score for UC. Three AI methods were compared. AI models were evaluated on held-back testing sets and model predictions were compared against an expert central reader and five independent pathologists. The model based on multiple instance learning and the attention mechanism (SA-AbMILP) demonstrated the best performance among competing models. AI modeled GHAS and Geboes sub-grades matched central readings with moderate to substantial agreement, with accuracies ranging from 65% to 89%. Furthermore, the model was able to distinguish the presence and absence of pathology across four selected histological features with accuracies for colon, in both CD and UC, ranging from 87% to 94% and, for CD ileum, ranging from 76% to 83%. For both CD and UC, and across anatomical compartments (ileum and colon) in CD, comparable accuracies against central readings were found between the model assigned scores and scores by an independent set of pathologists. Deep learning models based upon GHAS and Geboes scoring systems were effective at distinguishing between the presence and absence of IBD microscopic disease activity.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Histologic disease activity in Inflammatory Bowel Disease (IBD) is associated with clinical outcomes and is an important endpoint in drug development. We developed deep learning models for automating histological assessments in IBD.
METHODS METHODS
Histology images of intestinal mucosa from phase 2 and phase 3 clinical trials in Crohn's disease (CD) and Ulcerative Colitis (UC) were used to train artificial intelligence (AI) models to predict the Global Histology Activity Score (GHAS) for CD and Geboes histopathology score for UC. Three AI methods were compared. AI models were evaluated on held-back testing sets and model predictions were compared against an expert central reader and five independent pathologists.
RESULTS RESULTS
The model based on multiple instance learning and the attention mechanism (SA-AbMILP) demonstrated the best performance among competing models. AI modeled GHAS and Geboes sub-grades matched central readings with moderate to substantial agreement, with accuracies ranging from 65% to 89%. Furthermore, the model was able to distinguish the presence and absence of pathology across four selected histological features with accuracies for colon, in both CD and UC, ranging from 87% to 94% and, for CD ileum, ranging from 76% to 83%. For both CD and UC, and across anatomical compartments (ileum and colon) in CD, comparable accuracies against central readings were found between the model assigned scores and scores by an independent set of pathologists.
CONCLUSIONS CONCLUSIONS
Deep learning models based upon GHAS and Geboes scoring systems were effective at distinguishing between the presence and absence of IBD microscopic disease activity.

Identifiants

pubmed: 37814351
pii: 7303316
doi: 10.1093/ecco-jcc/jjad171
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation.

Auteurs

Dawid Rymarczyk (D)

Ardigen SA, Kraków, Poland.
Faculty of Mathematics and Computer Science, Jagiellonian University, Kraków, Poland.

Weiwei Schultz (W)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Adriana Borowa (A)

Ardigen SA, Kraków, Poland.
Faculty of Mathematics and Computer Science, Jagiellonian University, Kraków, Poland.

Joshua R Friedman (JR)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Tomasz Danel (T)

Ardigen SA, Kraków, Poland.
Faculty of Mathematics and Computer Science, Jagiellonian University, Kraków, Poland.

Patrick Branigan (P)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Michał Chałupczak (M)

Ardigen SA, Kraków, Poland.

Anna Bracha (A)

Ardigen SA, Kraków, Poland.

Tomasz Krawiec (T)

Ardigen SA, Kraków, Poland.

Michał Warchoł (M)

Ardigen SA, Kraków, Poland.

Katherine Li (K)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Gert De Hertogh (G)

Department of Pathology, University Hospitals KU Leuven, Belgium.

Bartosz Zieliński (B)

Ardigen SA, Kraków, Poland.
Faculty of Mathematics and Computer Science, Jagiellonian University, Kraków, Poland.

Louis R Ghanem (LR)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Aleksandar Stojmirovic (A)

Janssen Research & Development, LLC, Spring House, Pennsylvania.

Classifications MeSH