Evidence map›Paper›PMID 40293634›Full record

ArticleDigestive diseases and sciences2025

A Simple, Interpretable Machine Learning Model Based on Clinical Factors Accurately Predicts Incident Dysplasia or Malignancy in Barrett's Esophagus.

Ashwin Rao, Jasmine Haydel, Samuel Ma, Aaron P Thrift, Theresa Nguyen-Wenker, Hashem B El-Serag

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Article in Digestive diseases and sciences, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ashwin RaoSection of Gastroenterology and Hepatology, Baylor College of Medicine, Houston, TX, USA.
Jasmine HaydelDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Samuel MaDepartment of Internal Medicine, Baylor College of Medicine, Houston, TX, USA.
Aaron P ThriftSection of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX, USA.
Theresa Nguyen-WenkerSection of Gastroenterology and Hepatology, Baylor College of Medicine, Houston, TX, USA.
Hashem B El-SeragSection of Gastroenterology and Hepatology, Baylor College of Medicine, Houston, TX, USA. hasheme@bcm.edu.

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Hashem B El-Serag · 2001 to 2026
$28.3M
Research Training in GastroenterologyT32DK083266 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Hashem B El-Serag, FASIHA KANWAL · 2010 to 2026
$2.3M
NIDDK NIH HHS P30 DK056338NIDDK NIH HHS T32 DK083266NIH HHS P30DK056338
6 · The paper itself

Abstract

purposeIdentifying patients likely to develop dysplasia or malignancy is critical for effective surveillance in patients with Barrett's Esophagus (BE). However, current predictive models are limited. We evaluated the performance of machine learning (ML) models in predicting incident dysplasia or malignancy in a cohort of veteran patients with BE.

methodsWe analyzed data from 598 patients newly diagnosed with non-dysplastic BE (NDBE), BE indefinite for dysplasia (BE-IND), and BE with non-persistent low-grade dysplasia (LGD) at the Michael DeBakey Veterans Affairs Medical Center from November 1990 to January 2019 with follow-up through January 2024. Progressors were patients who developed persistent LGD, HGD, or EAC within 5 years of index endoscopy. Six models were evaluated, encompassing regression and ensemble-based ML methods.

resultsOf 598 qualifying patients, 61 (10.2%) progressed. Longer segments and indefinite/non-persistent LGD pathology were associated with higher risk of progression in unadjusted analyses. BE segment length remained significant on multivariate analysis (OR 1.26; 95% CI 1.17-1.36 per 1 cm increase). A decision tree (DT) model, using only segment length, achieved the highest discrimination (AUROC = 0.79) and excellent sensitivity (93.3%). The DT model also identified segment length thresholds for risk stratification: < 0.95 cm (minimal risk), 0.95-2.44 cm (low), 2.44-9.45 cm (moderate),  > 9.45 cm (high).

conclusionsA simple, interpretable DT model with segment length as the sole predictor outperformed regression and complex ML-based models in predicting BE progressors. Findings align with European Society of Gastrointestinal Endoscopy (ESGE) guidelines suggesting tailored surveillance based on segment length and provide actionable thresholds. These results offer a practical ML tool for BE surveillance.

Indexed as

AdenocarcinomaBarrett EsophagusEsophageal NeoplasmsMachine LearningPrecancerous ConditionsAgedDisease ProgressionEsophagoscopyFemaleHumansIncidenceMaleMiddle AgedPredictive Value of TestsRetrospective StudiesRisk AssessmentBarrett’s EsophagusClinical risk predictionEndoscopyMachine learningSurveillance

Identifiers

PMID40293634
PMCPMC12587488

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