Evidence map›Paper›PMID 41584263›Full record

ArticleJournal of pathology informatics2026

A machine learning model of lamina propria fibrosis in eosinophilic esophagitis for prediction of fibrostenotic disease.

Priyadharshini Sivasubramaniam, Abdelrahman Shabaan, Rofyda Elhalaby, Bashar Hasan, Ameya A Patil, Saadiya Nazli, Adilson DaCosta, Byoung Uk Park, Lindsey Smith, Taofic Mounajjed and 7 more

Abstract read
In one paragraph

Article in Journal of pathology informatics, 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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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

17 authors.

Priyadharshini SivasubramaniamPathology And Laboratory Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Abdelrahman ShabaanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Rofyda ElhalabyDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Bashar HasanDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Ameya A PatilDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Saadiya NazliDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Adilson DaCostaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Byoung Uk ParkDepartment of Pathology, University of Minnesota, Minneapolis, MN, USA.
Lindsey SmithMySME, LLC; Mayo Clinic, Rochester, MN, USA.
Taofic MounajjedDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Stephen M LaganaDepartment of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, USA.
Chamil CodipillyDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Puanani HopsonDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Imad AbsahDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Christopher P HartleyDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Rondell P GrahamDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Roger K MoreiraDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Eosinophilic esophagitis (EoE) is a chronic immune-mediated disease that can progress to fibrostenotic complications. Lamina propria fibrosis (LPF) plays a critical role in this progression but is difficult to assess reliably in routine biopsies. We aimed to develop and validate an artificial intelligence (AI) model to quantify LPF on hematoxylin and eosin (H&E)-stained slides and to evaluate its ability to predict fibrostenotic disease. Methods: We used a cloud-based platform (Aiforia Inc., Cambridge, MA, USA) to train a supervised AI model to recognize several histological features of EoE, including LPF. Our validation cohort consisted of 213 esophageal biopsy whole-slide images, including 100 adult and 113 pediatric samples with mucosal eosinophilia, which were prospectively evaluated in our anatomic pathology service between 2020 and 2021 using a standardized histological scoring system. AI-based LPF scores were correlated with the development of fibrostenotic disease on subsequent endoscopies after a median follow-up time of 31.4 months. Results: The AI fibrosis score correlated with pathologist-determined LPF (Spearman's Conclusion: This study demonstrates that AI-based quantification of LPF on routine H&E slides provides an objective and clinically meaningful assessment of fibrosis in EoE. The AI fibrosis score predicts fibrostenotic disease more consistently than conventional pathology evaluation and may improve risk stratification even in limited biopsy samples. Integration of digital pathology tools may enhance histological assessment of fibrosis in EoE and support clinical decision-making.

Indexed as

AIArtificial intelligenceDigital pathologyEosinophilic esophagitisEsophagusFibrosisHistological assessmentLamina propria fibrosisMachine learningPredictive modelingStenosisStrictureWhole-slide imaging

Identifiers

PMID41584263
PMCPMC12828521

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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.