Evidence map›Paper›PMID 40597688›Full record

ArticleBMC gastroenterology2025

Unveiling the diagnostic and pro-inflammatory role of crohn's disease: insights from 16 S-guided discovery and species-specific validation.

Yao Xu, Runxiang Xie, Yuqing Weng, Yewei Fang, Huimin Chen, Shuan Tao, He Zhang, Yawen Ye, Xinyu Deng, Axiang Han and 2 more

Abstract read
In one paragraph

Article in BMC gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Yao XuDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Runxiang XieDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Yuqing WengHealth Science Center, Ningbo University, Ningbo, 315211, China.
Yewei FangDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Huimin ChenDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Shuan TaoDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
He ZhangLaboratory Medical School, Bengbu Medical University, Bengbu, 233030, China.
Yawen YeCollege of Food Science and Engineering, Ningbo University, Ningbo, 315211, China.
Xinyu DengCollege of Food Science and Engineering, Ningbo University, Ningbo, 315211, China.
Axiang HanDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Qi JiangDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China. Jiangqigua@163.com.
Wei LiangDepartment of Clinical Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China. hslwys@163.com.

Funding

the Hospital-level Project of the First Affiliated Hospital of Ningbo University XGY2308the Key Project of Ningbo Municipal Science and Technology Bureau 2023j020the Medical Science and Technology Project of China 2022Y05the Population Welfare Foundation Medical Innovation Project of China SLB-6-20230912-351the Project Key R&D program of 2022 year of the Ningbo Science and Technology Bureau 2022z2202022
6 · The paper itself

Abstract

backgroundThe rising incidence of Crohn's disease (CD) in Asia underscores the need to explore its underlying mechanisms. The interaction between gut microbiota and the host is strongly linked to CD onset and progression, yet the precise mechanisms remain unclear. Previous studies have demonstrated that Ruminococcus gnavus (R. gnavus) is closely associated with the development and progression of CD. Therefore, this study focuses on the inflammatory role of R. gnavus in CD pathogenesis.

methodsWe performed comprehensive 16 S rRNA sequencing on fecal samples from active CD patients, inactive CD patients, and healthy controls. Alongside this, we conducted clinical data and correlation analyses. To identify key microbial genera, we developed and validated a random forest classification model. Additionally, we utilized a dextran sulfate sodium (DSS)-induced colitis model in C57BL/6 mice to explore the inflammatory role of R. gnavus (ATCC 29149).

resultsOur analysis revealed significant shifts in gut microbiome composition across different stages of CD compared to healthy controls. Notably, there was a marked decrease in Agathobacter and an increase in R. gnavus in patients with active CD. The random forest classification model, which was based on six specific genera (Agathobacter, Vicinamibacteraceae, Arthrobacter, Eubacterium coprostanoligenes group, Ruminococcus gnavus group, and Prevotella 9), achieved an AUC of 0.912, effectively distinguishing CD patients from healthy controls. In the DSS-induced colitis model, R. gnavus exacerbated inflammation, significantly increasing levels of IL-6 and TNF-α, and significantly decreasing levels of Claudin-1 and MUC2, further underscoring its critical role in CD pathogenesis.

conclusionThe identified genera demonstrate potential as diagnostic biomarkers for CD, with R. gnavus playing a key role in the disease's pathogenesis by inducing inflammation in colitis models.

Indexed as

Crohn DiseaseEubacterialesGastrointestinal MicrobiomeRuminococcusAdultAnimalsCase-Control StudiesColitisDextran SulfateDisease Models, AnimalFecesFemaleHumansInterleukin-6MaleMiceDextran SulfateInterleukin-6RNA, Ribosomal, 16SCrohn’s diseaseDisease activityGut microbiotaRandom forestRuminococcus gnavus

Identifiers

PMID40597688
PMCPMC12211897

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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.