A Pilot Study on Automatic Three-Dimensional Quantification of Barrett's Esophagus for Risk Stratification and Therapy Monitoring.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
09 2021
Historique:
received: 02 02 2021
revised: 10 05 2021
accepted: 27 05 2021
pubmed: 12 6 2021
medline: 18 1 2022
entrez: 11 6 2021
Statut: ppublish

Résumé

Barrett's epithelium measurement using widely accepted Prague C&M classification is highly operator dependent. We propose a novel methodology for measuring this risk score automatically. The method also enables quantification of the area of Barrett's epithelium (BEA) and islands, which was not possible before. Furthermore, it allows 3-dimensional (3D) reconstruction of the esophageal surface, enabling interactive 3D visualization. We aimed to assess the accuracy of the proposed artificial intelligence system on both phantom and endoscopic patient data. Using advanced deep learning, a depth estimator network is used to predict endoscope camera distance from the gastric folds. By segmenting BEA and gastroesophageal junction and projecting them to the estimated mm distances, we measure C&M scores including the BEA. The derived endoscopy artificial intelligence system was tested on a purpose-built 3D printed esophagus phantom with varying BEAs and on 194 high-definition videos from 131 patients with C&M values scored by expert endoscopists. Endoscopic phantom video data demonstrated a 97.2% accuracy with a marginal ± 0.9 mm average deviation for C&M and island measurements, while for BEA we achieved 98.4% accuracy with only ±0.4 cm The proposed methodology automatically extracts Prague C&M scores with high accuracy. Quantification and 3D reconstruction of the entire Barrett's area provides new opportunities for risk stratification and assessment of therapy response.

Sections du résumé

BACKGROUND & AIMS
Barrett's epithelium measurement using widely accepted Prague C&M classification is highly operator dependent. We propose a novel methodology for measuring this risk score automatically. The method also enables quantification of the area of Barrett's epithelium (BEA) and islands, which was not possible before. Furthermore, it allows 3-dimensional (3D) reconstruction of the esophageal surface, enabling interactive 3D visualization. We aimed to assess the accuracy of the proposed artificial intelligence system on both phantom and endoscopic patient data.
METHODS
Using advanced deep learning, a depth estimator network is used to predict endoscope camera distance from the gastric folds. By segmenting BEA and gastroesophageal junction and projecting them to the estimated mm distances, we measure C&M scores including the BEA. The derived endoscopy artificial intelligence system was tested on a purpose-built 3D printed esophagus phantom with varying BEAs and on 194 high-definition videos from 131 patients with C&M values scored by expert endoscopists.
RESULTS
Endoscopic phantom video data demonstrated a 97.2% accuracy with a marginal ± 0.9 mm average deviation for C&M and island measurements, while for BEA we achieved 98.4% accuracy with only ±0.4 cm
CONCLUSIONS
The proposed methodology automatically extracts Prague C&M scores with high accuracy. Quantification and 3D reconstruction of the entire Barrett's area provides new opportunities for risk stratification and assessment of therapy response.

Identifiants

pubmed: 34116029
pii: S0016-5085(21)03087-0
doi: 10.1053/j.gastro.2021.05.059
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

865-878.e8

Subventions

Organisme : Medical Research Council
ID : MC_UU_00008/7
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206314/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S036377/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_MR/S025952/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 109965/Z/15/Z
Pays : United Kingdom
Organisme : Department of Health
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12010/7
Pays : United Kingdom

Investigateurs

Philip Allan (P)
Tim Ambrose (T)
Carolina Arancibia-Cárcamo (C)
Ellie Barnes (E)
Elizabeth Bird-Lieberman (E)
Jan Bornschein (J)
Oliver Brain (O)
Jane Collier (J)
Emma Culver (E)
Alessandra Geremia (A)
Bruce George (B)
Lucy Howarth (L)
Kelsey Jones (K)
Paul Klenerman (P)
Rebecca Palmer (R)
Fiona Powrie (F)
Astor Rodrigues (A)
Jack Satsangi (J)
Alison Simmons (A)
Simon Travis (S)
Holm Uhlig (H)
Alissa Walsh (A)

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Sharib Ali (S)

Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom; Big Data Institute, University of Oxford, Li Ka Shing Centre for Health Information and Discovery, Oxford, United Kingdom. Electronic address: sharib.ali@eng.ox.ac.uk.

Adam Bailey (A)

Translational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom.

Stephen Ash (S)

Ludwig Institute for Cancer Research, University of Oxford, Oxford, United Kingdom.

Maryam Haghighat (M)

Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom; Big Data Institute, University of Oxford, Li Ka Shing Centre for Health Information and Discovery, Oxford, United Kingdom.
Translational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom.

Simon J Leedham (SJ)

Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom; Intestinal Stem Cell Biology Laboratory, Wellcome Trust Centre Human Genetics, University of Oxford, Oxford, United Kingdom.

Xin Lu (X)

Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom; Ludwig Institute for Cancer Research, University of Oxford, Oxford, United Kingdom.

James E East (JE)

Translational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom.

Jens Rittscher (J)

Institute of Biomedical Engineering, Department of Engineering Science, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom; Ludwig Institute for Cancer Research, University of Oxford, Oxford, United Kingdom; Big Data Institute, University of Oxford, Li Ka Shing Centre for Health Information and Discovery, Oxford, United Kingdom. Electronic address: jens.rittscher@eng.ox.ac.uk.

Barbara Braden (B)

Translational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, United Kingdom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford, United Kingdom. Electronic address: barbara.braden@ndm.ox.ac.uk.

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