Comparative molecular profiling of Helicobacter pylori infection and antibiotic genotypic resistance in paired gastric mucosa, gastric juice, and stool samples

Increasing antibiotic resistance in Helicobacter pylori (H. pylori) is undermining empirical eradication therapies. Non-invasive methods for resistance profiling are urgently needed to guide precision treatment. This study aimed to compare the performance of paired gastric juice and stool samples against gastric mucosa for the detection of H. pylori infection and genotypic resistance to clarithromycin and levofloxacin. In this prospective study, patients with H. pylori infection confirmed through positive <sup>13</sup>C/<sup>14</sup>C-urea breath test and histology (Warthin-Starry staining) provided matched gastric mucosal biopsies, gastric juice, and stool samples. Genotypic resistance to clarithromycin and levofloxacin was assessed via commercial quantitative PCR. Performance of gastric juice and stool samples were compared against gastric mucosa as the reference standard using sensitivity, specificity, predictive, and Cohen's kappa values. Among 218 patients with confirmed H. pylori infection, gastric mucosa identified clarithromycin resistance in 56.9% and levofloxacin resistance in 33.0%. For detecting infection, gastric juice achieved higher sensitivity (97.6% vs. 91.3%, P = 0.003) and specificity (50.0% vs. 30.0%), with stronger reference agreement (kappa = 0.476 vs. kappa = 0.025). In resistance genes profiling, gastric juice exhibited superior sensitivity for both clarithromycin (87.1% vs. 72.6%, P = 0.001) and levofloxacin (70.8% vs. 61.1%, P = 0.049), while maintaining high specificity (82.9% and 92.3%, respectively). Agreement with gastric mucosa was substantially higher for gastric juice (clarithromycin: kappa = 0.691; levofloxacin: kappa = 0.656) than for stool (kappa = 0.504 and kappa = 0.598, P < 0.05 for clarithromycin). Gastric juice also provided higher negative predictive values. Gastric juice shows better diagnostic performance and concordance with mucosal-based resistance genes profiling compared to stool. Furthermore, gastric juice sampling during endoscopy provides a reliable minimally invasive source for resistance profiling, which can serve as a high-quality alternative or backup to mucosal biopsies without the need for repeated invasive procedures.Registration: This clinical trial was registered at the Chinese Clinical Trial Registry (ChiCTR2400084465).

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Journal
Scientific Reports
Published
2025-12-21
DOI
https://doi.org/10.1038/s41598-025-32968-x
Primary Topic
Helicobacter pylori-related gastroenterology studies
Type
article
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article

Comparative molecular profiling of Helicobacter pylori infection and antibiotic genotypic resistance in paired gastric mucosa, gastric juice, and stool samples

Dongling Xie, J. Cheng, Mengyuan Yang, Zhen Li et al.
Scientific Reports
Helicobacter pylori-related gastroenterology studies
article

Comparative molecular profiling of Helicobacter pylori infection and antibiotic genotypic resistance in paired gastric mucosa, gastric juice, and stool samples

Dongling Xie, J. Cheng, Mengyuan Yang, Zhen Li, Xiaolin Zhao, Kun Huang, Yong Cai, Chanjuan Fan, Hui Wang
article en

Abstract

Increasing antibiotic resistance in Helicobacter pylori (H. pylori) is undermining empirical eradication therapies. Non-invasive methods for resistance profiling are urgently needed to guide precision treatment. This study aimed to compare the performance of paired gastric juice and stool samples against gastric mucosa for the detection of H. pylori infection and genotypic resistance to clarithromycin and levofloxacin. In this prospective study, patients with H. pylori infection confirmed through positive <sup>13</sup>C/<sup>14</sup>C-urea breath test and histology (Warthin-Starry staining) provided matched gastric mucosal biopsies, gastric juice, and stool samples. Genotypic resistance to clarithromycin and levofloxacin was assessed via commercial quantitative PCR. Performance of gastric juice and stool samples were compared against gastric mucosa as the reference standard using sensitivity, specificity, predictive, and Cohen's kappa values. Among 218 patients with confirmed H. pylori infection, gastric mucosa identified clarithromycin resistance in 56.9% and levofloxacin resistance in 33.0%. For detecting infection, gastric juice achieved higher sensitivity (97.6% vs. 91.3%, P = 0.003) and specificity (50.0% vs. 30.0%), with stronger reference agreement (kappa = 0.476 vs. kappa = 0.025). In resistance genes profiling, gastric juice exhibited superior sensitivity for both clarithromycin (87.1% vs. 72.6%, P = 0.001) and levofloxacin (70.8% vs. 61.1%, P = 0.049), while maintaining high specificity (82.9% and 92.3%, respectively). Agreement with gastric mucosa was substantially higher for gastric juice (clarithromycin: kappa = 0.691; levofloxacin: kappa = 0.656) than for stool (kappa = 0.504 and kappa = 0.598, P < 0.05 for clarithromycin). Gastric juice also provided higher negative predictive values. Gastric juice shows better diagnostic performance and concordance with mucosal-based resistance genes profiling compared to stool. Furthermore, gastric juice sampling during endoscopy provides a reliable minimally invasive source for resistance profiling, which can serve as a high-quality alternative or backup to mucosal biopsies without the need for repeated invasive procedures.Registration: This clinical trial was registered at the Chinese Clinical Trial Registry (ChiCTR2400084465).

Scientific ReportsVol. 16(1)
Aviation General Hospital (CN)
Openalex Percentile: Top 39%
Helicobacter pylori-related gastroenterology studies
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