Evidence map›Paper›PMID 38928402›Full record

ArticleInternational journal of molecular sciences2024

Integrated Analysis of Microbiome and Metabolome Reveals Disease-Specific Profiles in Inflammatory Bowel Diseases and Intestinal Behçet's Disease.

Yehyun Park, Jae Bum Ahn, Da Hye Kim, I Seul Park, Mijeong Son, Ji Hyung Kim, Hyun Woo Ma, Seung Won Kim, Jae Hee Cheon

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Current research in food science · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. 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

9 authors.

Yehyun ParkDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.ORCID 0000-0001-8811-0631
Jae Bum AhnDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Da Hye KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
I Seul ParkDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.ORCID 0000-0001-6546-5456
Mijeong SonDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Ji Hyung KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Hyun Woo MaDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Seung Won KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Jae Hee CheonDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

Funding

Handok-Yonsei University College of Medicine, Department of Internal Medicine research fund HANDOK 2017-004Mid-career Researcher Program through NRF grant funded by the Korea government (MSIP) NRF-2017R1A2B4001848Research Program of the Korea Medical Institute pending
6 · The paper itself

Abstract

The gut microbial and metabolic characteristics of intestinal Behçet's disease (BD), a condition sharing many clinical similarities with ulcerative colitis (UC) and Crohn's disease (CD), are largely unexplored. This study investigated the gut microbial and metabolic characteristics of intestinal BD as well as potential biomarkers, comparing them with those in UC, CD, and healthy controls. Colon tissue and stool samples from 100 patients (35 UC, 30 CD, and 35 intestinal BD) and 41 healthy volunteers were analyzed using 16S ribosomal RNA sequencing to assess microbial diversity, taxonomic composition, and functional profiling. Plasma metabolomic analyses were performed using gas chromatography and ultra-performance liquid chromatography-mass spectrometry. Results indicated reduced microbial diversity in CD but not in intestinal BD, with intestinal BD showing fewer changes compared to controls yet distinct taxonomic features from UC, CD, and controls. Common alterations across all diseases included a reduction in beneficial bacteria producing short-chain fatty acids. Intestinal BD-specific changes featured a decreased abundance of Bacteroides fragilis. Metabolomic profiles in intestinal BD were similar to those in CD but distinct from those in UC, displaying significant changes in energy metabolism and genetic information processing. This integrative analysis revealed both shared and unique profiles in intestinal BD compared with UC, CD, and controls, advancing our understanding of the distinctive features of these diseases.

Indexed as

Behcet SyndromeGastrointestinal MicrobiomeMetabolomeAdultBiomarkersCase-Control StudiesColitis, UlcerativeCrohn DiseaseFecesFemaleHumansInflammatory Bowel DiseasesMaleMetabolomicsMiddle AgedRNA, Ribosomal, 16SBiomarkersRNA, Ribosomal, 16SCrohn’s diseaseintestinal Behçet’s diseasemetabolomemicrobiomemulti-omicsulcerative colitis

Identifiers

PMID38928402
PMCPMC11203907

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.