Evidence map›Paper›PMID 37661264›Full record

ArticleBMC microbiology2023

Integration of taxa abundance and occurrence frequency to identify key gut bacteria correlated to clinics in Crohn's disease.

Xunchao Cai, Nan Zhou, Qian Zou, Yao Peng, Long Xu, Lijuan Feng, Xiaowei Liu

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Xunchao CaiDepartment of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen, 518055, China.
Nan ZhouDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, China.
Qian ZouDepartment of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen, 518055, China.
Yao PengDepartment of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen, 518055, China.
Long XuDepartment of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen, 518055, China.
Lijuan FengDepartment of Gastroenterology and Hepatology, Shenzhen University General Hospital, Shenzhen, 518055, China. fenglj@szu.edu.cn.
Xiaowei LiuDepartment of Gastroenterology, Xiangya Hospital, Central South University, Changsha, 410008, China. liuxw@csu.edu.cn.
Shenzhen University · CNCentral South University · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteria abundance alternation in the feces or mucosa of Crohn's disease (CD) patients has long been applied to identify potential biomarkers for this disease, while the taxa occurrence frequency and their correlations with clinical traits were understudied. A total of 97 samples from the feces and gut mucosa were collected from CD patients and healthy controls (HCs), 16S rRNA-based analyses were performed to determine the changes in taxa abundance and occurrence frequency along CD and to correlate them with clinical traits. The results showed that bacteria communities were divergent between feces and mucosa, while the taxa abundance and occurrence frequency in both partitions showed similar exponential correlations. The decrease of specific fecal bacteria was much more effective in classifying the CD and HCs than that of the mucosal bacteria. Among them, Christensenellaceae_R-7_group and Ruminococcus were predicted as biomarkers by using random forest algorithm, which were persistently presented (> 71.40% in frequency) in the feces of the HCs with high abundance, whereas transiently presented in the feces (< 5.5% in frequency) and mucosa (< 18.18% in frequency) of CD patients with low abundance. Co-occurrence network analysis then identified them as hub taxa that drive the alternations of other bacteria and were positively correlated to the circuiting monocytes. The loss of specific bacteria in the healthy gut may cause great disturbance of gut microbiota, causing gut bacteria dysbiosis and correlated to immune disorders along CD, which might not only be developed as effective noninvasive biomarkers but also as therapy targets.

Indexed as

Crohn DiseaseBacteriaDysbiosisEubacterialesHumansRNA, Ribosomal, 16SRNA, Ribosomal, 16SCo-occurrence networkCrohn’s diseaseMucosal and fecal microbiotaOccurrence frequency

Identifiers

PMID37661264
PMCPMC10476393
OpenAlexW4386407143

What OpenQuestion holds

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LicenceCC BY
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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.