Evidence map›Paper›PMID 36969184›Full record

ArticleFrontiers in immunology2023

Integrating microbiome and metabolome revealed microbe-metabolism interactions in the stomach of patients with different severity of peptic ulcer disease.

Chao Wang, Xiao Yu, Hongqiang Lin, Guoqiang Wang, Jianming Liu, Chencheng Gao, Mingran Qi, Dan Wang, Fang Wang

Open access · goldFull text read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Review
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4 · The record

Corrections and comments

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

9 authors at 2 institutions in 1 country.

Chao WangDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Xiao YuDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Hongqiang LinDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Guoqiang WangDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Jianming LiuDepartment of Otolaryngology Head and Neck Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.
Chencheng GaoDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Mingran QiDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Dan WangDepartment of Gastroenterology, First Hospital of Jilin University, Changchun, China.
Fang WangDepartment of Pathogen Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Jilin University · CNJilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Peptic ulcer disease (PUD) is a multi-cause illness with an unknown role for gastric flora and metabolism in its pathogenesis. In order to further understand the pathogenesis of gastric flora and metabolism in PUD, this study used histological techniques to analyze the microbiome and metabolome of gastric biopsy tissue. In this paper, our work described the complex interactions of phenotype-microbial-metabolite-metabolic pathways in PUD patients at different pathological stages. Methods: Gastric biopsy tissue samples from 32 patients with chronic non-atrophic gastritis, 24 patients with mucosal erosions, and 8 patients with ulcers were collected for the microbiome. UPLC-MS metabolomics was also used to detect gastric tissue samples. These datasets were analyzed individually and integrated using various bioinformatics methods. Results: Our work found reduced diversity of gastric flora in patients with PUD. PUD patients at different pathological stages presented their own unique flora, and there were significant differences in flora phenotypes. Conclusion: Our research results provided substantial evidence to support some data on the analysis of the microbial community and its metabolism in the stomach, and they demonstrated many specific interactions between the gastric microbiome and the metabolome. Our study can help reveal the pathogenesis of PUD and indicate plausible disease-specific mechanisms for future studies from a new perspective.

Indexed as

Gastritis, AtrophicMicrobiotaPeptic UlcerChromatography, LiquidHumansMetabolomeTandem Mass Spectrometrycomprehensive analysisgastric florametabolomemicrobiomepeptic ulcer

Identifiers

PMID36969184
PMCPMC10034094
OpenAlexW4323665771

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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.