Evidence map›Paper›PMID 41957592›Full record

ArticleBMC gastroenterology2026

The LGR5/TFF2 ratio as a stem cell biomarker predicts high-risk status in chronic atrophic gastritis: a retrospective cohort study.

Qingqing Zhang, Di Wu, Fengyun Guo, Shengnan Yang, Lijing Bao, Ruiying Zhang, Ping Wang

Abstract read
In one paragraph

Article in BMC gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Research Status and Prospects ofGastroenterology research and practice · 2026
    Review
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Qingqing ZhangInstitute of Digestive Diseases, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China.
Di WuFirst Affiliated Hospital of Heilongjiang University of Traditional Chinese Medicine, Harbin, 150040, China.
Fengyun GuoInstitute of Digestive Diseases, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China.
Shengnan YangGraduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
Lijing BaoInstitute of Digestive Diseases, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China.
Ruiying ZhangGraduate School, Beijing University of Chinese Medicine, Beijing, 100029, China.
Ping WangInstitute of Digestive Diseases, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, 100091, China. celia_1224@163.com.

Funding

Beijing Municipal Health Commission Research-Oriented Ward Construction Project No. BCRW202108the National Science and Technology Major Program 2024ZD0521003
6 · The paper itself

Abstract

backgroundChronic atrophic gastritis (CAG) severity risk assessment remains challenging due to limitations of current static histologic/endoscopic tools. We evaluated the leucine-rich repeat-containing G-protein coupled receptor 5 (LGR5)/trefoil factor 2 (TFF2) ratio - quantifying gastric stem cell niche imbalance- as a dynamic biomarker for high-risk CAG (OLGA/OLGIM III-IV).

methodsIn a retrospective cohort (n = 60 CAG patients), we constructed four prediction models (Baseline: demographics; Clinical: +H. pylori/family history; Endoscopic; Full: +LGR5/TFF2 ratio) using Firth penalized regression. Model performance was assessed via area under the curve (AUC), Akaike (AIC), and Bayesian (BIC) information criteria, and likelihood ratio tests. Restricted cubic splines and subgroup analyses validated threshold effects.

resultsThe LGR5/TFF2 ratio > 1.066 (AUC = 0.93) identified high-risk CAG with 48.5-fold increased odds (95% CI: 4.07-578.51, P = 0.002), outperforming endoscopic/histologic models (ΔAUC = + 0.15). A nonlinear dose-response relationship revealed sharp risk escalation beyond this threshold. The high-ratio group (n = 20) exhibited 60.00% prevalence of prior H. pylori eradication, Wnt activation (β-catenin↑32.3%, CyclinD1↑90%, P < 0.001), and stronger endoscopic correlation (ρ = 0.42 for IM nodules) than traditional factors (ρ = 0.28 for H. pylori).

conclusionThe LGR5/TFF2 ratio is the first biomarker to molecularly define CAG severity risk by quantifying stem cell niche imbalance (LGR5↑/TFF2↓), achieving superior accuracy (AUC = 0.93) and identifying high-risk cases missed by current methods. Its integration into clinical practice could transform risk-stratified surveillance paradigms.

Indexed as

Gastritis, AtrophicReceptors, G-Protein-CoupledTrefoil Factor-2AdultAgedBiomarkersChronic DiseaseFemaleHelicobacter InfectionsHelicobacter pyloriHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentStem Cell NicheBiomarkersLGR5 protein, humanReceptors, G-Protein-CoupledTrefoil Factor-2Chronic atrophic gastritisFirth regressionLGR5/TFF2 ratioRisk stratificationStem cell niche imbalance

Identifiers

PMID41957592
PMCPMC13181973

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Registered trials

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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.