Evidence map›Paper›PMID 40904740›Full record

ArticleJournal of oral microbiology2025

Functional and taxonomic dysbiosis of the supragingival plaque metagenome in Behçet's disease.

Thanyarat Sapthanakorn, Pitipol Choopong, Wasawat Sermsripong, Chatkoew Boriboonhirunsarn, Chompak Khamwachirapitak, Annop Krasaesin, Pimchanok Sutthiboonyaphan, Nisachon Siripaiboonpong, Rangsini Mahanonda, Paswach Wiriyakijja and 3 more

Abstract read
In one paragraph

Article in Journal of oral microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

13 authors.

Thanyarat SapthanakornDepartment of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Pitipol ChoopongDepartment of Ophthalmology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-8857-8488
Wasawat SermsripongDepartment of Ophthalmology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Chatkoew BoriboonhirunsarnDental Department, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Chompak KhamwachirapitakCenter of Excellence in Medicine and Digital Health, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Annop KrasaesinCenter of Excellence in Medicine and Digital Health, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Pimchanok SutthiboonyaphanDepartment of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Nisachon SiripaiboonpongDepartment of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Rangsini MahanondaDepartment of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Paswach WiriyakijjaDepartment of Oral Medicine, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
George PelekosDivision of Periodontology and Implant Dentistry, Faculty of Dentistry, The University of Hong Kong, Hong Kong SAR, China.
Thantrira PorntaveetusCenter of Excellence in Medicine and Digital Health, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0003-0145-9801
Supreda Suphanantachat SrithanyaratDepartment of Periodontology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0001-6272-8169

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Behçet's Disease (BD), a complex autoinflammatory disorder, is increasingly linked to microbial dysbiosis, yet the specific microbial signatures and their functional consequences remain incompletely characterized. Elucidating these alterations is crucial for understanding BD pathogenesis. Objective: To identify distinct microbial community structures and functional potentials in supragingival plaque microbiomes of BD patients versus healthy controls (HC) using high-resolution shotgun metagenomic sequencing. Methods: Supragingival plaque from 18 BD patients and 22 HCs was subjected to shotgun metagenomics. Analyses included alpha/beta diversity, taxonomic composition, and MetaCyc pathway abundance, with statistical comparisons. Results: Despite similar age and clinical attachment levels, BD patients exhibited significantly increased alpha diversity and distinct beta diversity compared to HCs. Differential abundance analysis revealed an enrichment of anaerobic and opportunistic taxa in BD (implicating 4 phyla and 28 genera), alongside 19 significantly altered MetaCyc pathways, indicating substantial functional reprogramming within the BD oral microbiome. Conclusion: This high-resolution metagenomic analysis reveals profound oral microbiome dysbiosis in Behçet's Disease, characterized by altered diversity, a distinct taxonomic signature enriched with pathobionts, and significant functional shifts. These comprehensive microbial alterations are implicated in contributing to the local and systemic inflammatory processes driving BD pathogenesis, offering potential avenues for diagnostic biomarkers and targeted therapies.

Indexed as

Behçet’s diseasehealth disparityImmunityoral microbiomespirochete

Identifiers

PMID40904740
PMCPMC12404063

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