Evidence map›Paper›PMID 40416302›Full record

ArticleGastroenterology & hepatology2025

Enhancing the Diagnostic Yield of EGD for Diagnosis of Barrett Esophagus Through Methylated DNA Biomarker Triage.

Jayde E Kurland, Sheena B Patel, Richard Englehardt, Seper Dezfoli, Daniel M Tseng, Michael W Foutz, Paul S Bradley, Badi Eghterafi, Victoria T Lee, Suman Verma and 2 more

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Article in Gastroenterology & hepatology, 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

12 authors.

Jayde E KurlandGastro Health, Lima, Ohio.
Sheena B PatelGastro Health, Lima, Ohio.
Richard EnglehardtBariatric Medical Institute of Texas, San Antonio, Texas.
Seper DezfoliNorthwest Minimally Invasive Surgery, Portland, Oregon.
Daniel M TsengNorthwest Minimally Invasive Surgery, Portland, Oregon.
Michael W FoutzAdvanced Family Medicine, Kuna, Idaho.
Paul S BradleySavii Health, Savannah, Georgia.
Badi EghterafiValley Hospital Medical Center, Las Vegas, Nevada.
Victoria T LeeLucid Diagnostics, New York, New York.
Suman VermaLucid Diagnostics, New York, New York.
Brian J deGuzmanLucid Diagnostics, New York, New York.
Lishan AklogLucid Diagnostics, New York, New York.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEsoGuard (EG) is a methylated DNA assay for cells collected nonendoscopically with EsoCheck for detection of Barrett esophagus (BE) and can be utilized as a triage to esophagogastroduodenoscopy (EGD) in patients meeting clinical criteria for BE screening. EG triage may enrich the population undergoing EGD, increasing BE diagnosis without overburdening endoscopy resources.

aimTo test the hypothesis that EGDs performed on patients who test positive on EG have higher diagnostic yields than screening EGDs alone.

methodsWe collected real-world retrospective data from EG-positive patients for whom EGD diagnoses were available. The diagnostic yield of these EGDs was measured by the BE detection rate. The yield of screening EGDs was estimated by literature-established disease prevalence (10.6%). The hypothesis was tested using t-test for single proportions at a one-sided 5% significance level.

resultsAmong 209 patients, 60 (28.7%) had specialized intestinal metaplasia but 10 (4.8%) had less than 1 cm of nondysplastic disease. Because the American College of Gastroenterology (ACG) definition of BE requires disease length of at least 1 cm, these patients were excluded from analysis. In the analyzed population, we observed a 2.4-fold increase in BE detection compared with the 10.6% performance goal. There was a 2.7-fold increase in the cohort meeting ACG screening criteria and a 2.5-fold increase among those meeting ACG criteria who were aged 65 years and older.

conclusionEG triage enriches the population undergoing EGD for BE detection. Compared with screening EGD alone, it improves diagnostic yield. This may help direct more efficient use of endoscopy resources to improve disease detection in at-risk patients.

Indexed as

Barrett esophagusEsoCheckEsoGuardesophagogastroduodenoscopymethylated DNA biomarkernon-endoscopic screening

Identifiers

PMID40416302
PMCPMC12100536

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