Evidence map›Paper›PMID 42286710›Full record

ArticleGut pathogens2026

Integrated analysis of gastric microbiome and clinical features for the diagnosis of gastric neoplasms.

Donghoon Kang, Youngjin Shin, Yu Kyung Cho, Jae Myung Park, Seung-Hyun Jung, Myung-Gyu Choi

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Article in Gut pathogens, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Donghoon Kang *Department of Internal medicine, Seoul St. Mary's hospital, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Youngjin Shin *Basic Medical Science Facilitation Program, Catholic Medical Center, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Yu Kyung ChoDepartment of Internal medicine, Seoul St. Mary's hospital, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Jae Myung ParkDepartment of Internal medicine, Seoul St. Mary's hospital, The Catholic University of Korea, Seoul, 06591, Republic of Korea.
Seung-Hyun JungDepartment of Biochemistry, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul, 06591, Republic of Korea. hyun@catholic.ac.kr.
Myung-Gyu ChoiDepartment of Internal medicine, Seoul St. Mary's hospital, The Catholic University of Korea, Seoul, 06591, Republic of Korea.

Funding

Korean College of Helicobacter and Upper Gastrointestinal Research KCHUGR -201902503Ministry of Health and Welfare HI22C0226National Research Foundation of Korea RS-2024-00450891
6 · The paper itself

Abstract

backgroundGastric cancer (GC) progression is closely associated with microbial dysbiosis. However, microbial alterations in the intermediate stage of gastric adenoma (GA) remain under-characterized. This study investigated stage-specific microbiome changes and evaluated predictive models integrating microbial and clinical features.

methodsWe analyzed 231 subjects (129 GA, 73 GC, 29 healthy controls [HC]) using 16 S ribosomal DNA sequencing of paired oral, non-lesional gastric mucosa (GM), and gastric lesion (GL) samples. Random Forest models were constructed using microbial genera and clinical features, validated via leave-one-out cross-validation.

resultsStepwise microbial dysbiosis was observed during GC progression. Alpha diversity was significantly lower in GC-GL than in HC-GM and GA-GL. Helicobacter pylori infection was associated with reduced alpha diversity in GL samples. Genera such as Streptococcus, Neisseria, and Haemophilus were enriched in GC-GL, while Phocaeicola, Faecalibacterium, and Bifidobacterium were depleted. A gastric neoplasm prediction model incorporating 33 microbial genera and six clinical variables (age, sex, BMI, hypertension, smoking, and atrophy) demonstrated superior predictive performance (AUC = 0.830) in distinguishing gastric neoplasms from HCs, compared to models using either microbial genera (AUC = 0.790) or clinical variables (AUC = 0.715) alone. The combined model also accurately distinguished between GA and GC (AUC = 0.807).

conclusionsThe gastric microbiome profile changes dynamically during GC progression, highlighting its potential role in tumor development. Integrating microbial signatures with clinical features enables robust classification of gastric neoplasms and may serve as a valuable adjunctive tool for diagnosis and risk stratification in endoscopic practice.

Indexed as

16S rDNA sequencingEndoscopic resectionGastric adenomaGastric carcinomaMicrobiome

Identifiers

PMID42286710
PMCPMC13520268

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