Evidence map›Paper›PMID 42611818›Full record

ArticleJournal of Crohn's & colitis2026

Automated AI-based Mayo Endoscopic Scoring for ulcerative colitis across adult and pediatric cohorts from diverse populations.

Kamal Hammouda, Rishi Dakarapu, Chathruckan Rajendra, Hyojeong Lee, Sahar Almahfouz Nasser, Sharmistha Rudra, Vasantha Kolachala, Caitlin Diefendorf, Irina Geiculescu, Sushma Maddipatla and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of Crohn's & colitis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Kamal HammoudaWallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, United States.ORCID 0000-0003-1598-4287
Rishi DakarapuWallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, United States.
Chathruckan RajendraDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Hyojeong LeeWallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, United States.
Sahar Almahfouz NasserWallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, United States.
Sharmistha RudraDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Vasantha KolachalaDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Caitlin DiefendorfDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Irina GeiculescuDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Sushma MaddipatlaDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.
Anant MadabhushiWallace H. Coulter Department of Biomedical Engineering, Emory University and Georgia Institute of Technology, Atlanta, GA, 30322, United States.
Subra KugathasanDepartment of Pediatrics & Pediatric Research Institute, Emory University, Atlanta, GA, 30322, United States.ORCID 0000-0002-8686-4189

Funding

Pathology CoreU54CA254566 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MADABHUSHI, ANANT · 2020 to 2024
$5.0M
Oral Cavity Quantitative Histomorphometric Risk Classifier (OHbIC) in Oral Cavity Squamous Cell Carcinoma (OC-SCC)R01CA249992 · NCI · EMORY UNIVERSITY · PI LEWIS, JAMES, MADABHUSHI, ANANT · 2021 to 2025
$3.2M
Computerized histologic image predictor of cancer outcomeR01CA202752 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI FELDMAN, MICHAEL D, GANESAN, SHRIDAR · 2016 to 2020
$3.1M
Prostate cancer risk stratification via computational 3D pathologyR01CA268207 · NCI · UNIVERSITY OF WASHINGTON · PI Jonathan T.C. Liu, Anant Madabhushi · 2022 to 2026
$3.1M
Quantitative Histomorphometric Risk Classifier (QuHbIC) in HPV + Oropharyngeal CarcinomaR01CA220581 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KOYFMAN, SHLOMO, LEWIS, JAMES · 2018 to 2023
$3.1M
Computerized Histologic Risk Predictor (CHiRP) for Early Stage Lung CancersR01CA216579 · NCI · EMORY UNIVERSITY · PI FU, PINGFU, LLOYD, MARK · 2018 to 2023
$3.1M
Prognostic and Predictive Digital Tissue Image Assay for Prostate CancerR01CA268287 · NCI · EMORY UNIVERSITY · PI GUPTA, SHILPA, LAL, PRITI · 2022 to 2025
$3.0M
MR Fingerprinting and Computerized Decision Support for Prostate CancerR01CA208236 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GULANI, VIKAS, PONSKY, LEE EVAN · 2017 to 2022
$3.0M
Novel Radiomics for Predicting Response to Immunotherapy for Lung CancerR01CA257612 · NCI · EMORY UNIVERSITY · PI Anant Madabhushi, Vamsidhar Velcheti · 2021 to 2026
$2.7M
Research Training in Translational Gastroenterology and HepatologyT32DK108735 · NIDDK · EMORY UNIVERSITY · PI SUBRA KUGATHASAN · 2016 to 2026
$2.6M
An AI-enabled Digital Pathology Platform for Multi-Cancer Diagnosis, Prognosis and Prediction of Therapeutic BenefitU01CA269181 · NCI · EMORY UNIVERSITY · PI Anant Madabhushi, tanuja shet · 2022 to 2026
$2.5M
RadxTools for assessing tumor treatment response on imagingU01CA248226 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI TIWARI, PALLAVI, VISWANATH, SATISH EASWAR · 2020 to 2022
$1.4M
Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute 1U01CA239055-01Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute 1U01CA248226-01Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute 1U54CA254566-01Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA202752-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA208236-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA216579-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA220581-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA249992-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA257612-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA268207-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute R01CA268287-01A1Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute T32DK108735Cancer Tissue and Pathology shared resource of Winship Cancer Institute of Emory University and the National Cancer Institute U01CA269181NCI NIH HHS R01 CA202752NCI NIH HHS R01 CA208236NCI NIH HHS R01 CA216579NCI NIH HHS R01 CA220581NCI NIH HHS R01 CA249992NCI NIH HHS R01 CA257612NCI NIH HHS R01 CA268207NCI NIH HHS R01 CA268287NCI NIH HHS U01 CA239055NCI NIH HHS U01 CA248226NCI NIH HHS U01 CA269181NCI NIH HHS U54 CA254566NIDDK NIH HHS T32 DK108735NIH HHSUnited States GovernmentU.S. Department of Veterans Affairs, Department of Defense
6 · The paper itself

Abstract

backgroundEndoscopic assessment in ulcerative colitis (UC) is critical for clinical decision-making but limited by interobserver variability. AI-powered systems may improve consistency, but dataset heterogeneity has hindered clinical translation. We developed and evaluated a deep learning framework for standardized Mayo Endoscopic Score (MES) prediction across adult and pediatric populations from diverse regions. PATIENTS AND

methodsUsing three multi-institutional datasets, we trained and validated convolutional neural network models to predict MES. The primary dataset (LIMUC; 564 adults, 11 276 images, Turkey) supported model development, with external validation on TMC (308 adults, 7978 images, China) and the Emory Pediatric dataset (EPC; 80 children, 113 images, USA). Two models were developed: UC-Re for binary remission classification (MES 0-1 vs 2-3) and UC-MES for four-class grading (MES 0-3). Imaging artifacts were corrected using inpainting, and Fourier-Spatial Image Harmonization (FSIH) mitigated inter-institutional domain shifts. Performance was evaluated using area under the operating characteristic curve (AUC), F1-score, and quadratic weighted kappa (QWK).

resultsUC-Re achieved AUCs of 0.98, 0.95, and 0.98 across LIMUC, TMC, and EPC, with F1-scores of 0.92, 0.87, and 0.93, respectively. UC-MES demonstrated strong ordinal consistency (QWK = 0.81-0.85), comparable to inter-expert agreement (QWK = 0.88). Most misclassifications occurred between adjacent MES categories, reflecting human-like patterns.

conclusionsThis novel AI-based framework predicts MES across geographically diverse adult and pediatric UC datasets. Its strong performance, including comparability to expert gastroenterologists in EPC, supports its potential as a decision-support tool for standardized endoscopic monitoring. However, prospective multicenter validation is warranted prior to routine clinical implementation.

Indexed as

Colitis, UlcerativeColonoscopyDeep LearningAdolescentAdultChildConvolutional Neural NetworksFemaleHumansMaleMiddle AgedObserver VariationSeverity of Illness Indexdeep learningdomain shiftMayo Endoscopic Score (MES)pediatric and adultulcerative colitis (UC)

Identifiers

PMID42611818
PMCPMC13484516

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.