Evidence map›Paper›PMID 42676736›Full record

ArticleFrontiers in microbiology2026

Correlation between oral microbiome characteristics and clinical phenotypes in patients with GERD and its changes after anti-reflux surgery.

ZhongYu Wang, Yu Liu, Zhe Han, Fan-Ke Wang

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Article in Frontiers in microbiology, 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

4 authors.

ZhongYu Wang *Gastrointestinal Disease Center, The First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yu Liu *Hebei Medical University, Shijiazhuang, Hebei, China.
Zhe Han *Gastrointestinal Disease Center, The First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Fan-Ke Wang *Gastrointestinal Disease Center, The First Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastroesophageal reflux disease is defined by the reflux of gastroduodenal material into the esophagus, leading to troublesome symptoms and complications. Although the gastrointestinal microbiome has been increasingly implicated in gastroesophageal reflux disease pathogenesis, existing research has largely centered on esophageal and intestinal microbiota. The alterations and clinical relevance of the oral microbiome in gastroesophageal reflux disease remain underexplored. Therefore, this study was designed to: (1) systematically compare the oral microbiome structure between gastroesophageal reflux disease patients and healthy controls, and to examine the correlations between differentially abundant microbial taxa and key clinical phenotypes; (2) longitudinally assess the dynamic changes in the oral microbiome after anti-reflux surgery. Methods: We conducted a study integrating a case-control design with a longitudinal self-controlled component. Initially, 40 patients and 20 healthy volunteers were enrolled. Following exclusions based on diagnostic confirmation, 36 gastroesophageal reflux disease patients comprised the preoperative group (Group Pre), and 17 age-, gender-, and BMI-matched healthy volunteers served as controls (Group HC). Non-stimulated whole saliva samples were collected from all participants. A subgroup of 18 patients from Group Pre subsequently underwent laparoscopic fundoplication. Their saliva samples collected 3 months postoperatively constituted the postoperative group (Group Post) for longitudinal comparison. The V3-V4 hypervariable regions of the bacterial 16S rRNA gene were amplified and sequenced using high-throughput sequencing. Sequencing data were processed and analyzed with bioinformatics pipelines to evaluate α- and β-diversity. Differential microbial features across groups were identified using Linear Discriminant Analysis Effect Size. Correlations between microbial relative abundance and clinical parameters were assessed Results: (1) Cross-sectional comparisons: no significant differences were observed in α-diversity indices (ACE, Chao1, Shannon, and Simpson; all Conclusion: Our study demonstrates that gastroesophageal reflux disease is characterized by a specific oral dysbiosis, with the abundance of particular bacterial taxa correlating with clinical disease severity. Although laparoscopic anti-reflux surgery did not drastically alter the global oral microbiome architecture, it induced a targeted ecological shift. This shift was marked by the suppression of pro-inflammatory taxa, an increase in potentially beneficial commensals, and a trend toward restored α-diversity. These findings suggest that laparoscopic anti-reflux surgery may facilitate a shift of the oral microbiome toward a healthier ecological state following restoration of the anti-reflux barrier function. This observation provides a new microbiological perspective for understanding the broader physiological impact of anti-reflux surgery.

Indexed as

anti-reflux surgeryclinical phenotypesgastroesophageal reflux diseaselaparoscopic fundoplicationoral microbiome

Identifiers

PMID42676736
PMCPMC13526963

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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.