Evidence map›Paper›PMID 41056245›Full record

ArticlePloS one2025

Oral microbiome dysbiosis in acute ischemic stroke and transient ischemic attack patients.

Duangnapa Roongpiboonsopit, Sirikanya Wairit, Chichaya Nithisathienchai, Akkharin Pakdee, Thanya Cheibchalard, Jarun Sayasathid, Alisa Wilantho, Sissades Tongsima, Naraporn Somboonna

Abstract read
In one paragraph

Article in PloS one, 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
  2. Potential of Saliva in Stroke Patients: A Review.International journal of molecular sciences · 2026
    Review
  3. Review
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.

Duangnapa RoongpiboonsopitDivision of Neurology, Department of Medicine, Faculty of Medicine, Naresuan University, Phitsanulok, Thailand.ORCID https://orcid.org/0000-0002-7158-8687
Sirikanya WairitStroke Unit, Naresuan University Hospital, Phitsanulok, Thailand.
Chichaya NithisathienchaiDivision of Neurology, Department of Medicine, Faculty of Medicine, Naresuan University, Phitsanulok, Thailand.ORCID https://orcid.org/0000-0001-5114-9241
Akkharin PakdeeQuality Assurance Department, Faculty of Medicine, Naresuan University Hospital, Phitsanulok, Thailand.
Thanya CheibchalardDepartment of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
Jarun SayasathidCardiac Center, Naresuan University Hospital, Naresuan University, Phitsanulok, Thailand.
Alisa WilanthoNational Biobank of Thailand, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency, Pathum Thani, Thailand.
Sissades TongsimaNational Biobank of Thailand, National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency, Pathum Thani, Thailand.
Naraporn SomboonnaDepartment of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.ORCID https://orcid.org/0000-0002-7830-3509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oral microbiome (bacterial community) may influence systemic inflammation and vascular health, which both are critical factors in a pathogenesis of ischemic stroke. This study aimed to evaluate differences in the saliva microbiome of acute ischemic stroke (AIS) and transient ischemic attack (TIA) patients compared with matched healthy controls, hypothesizing that AIS and TIA patients are associated with oral microbiome shift. A prospective case-control study was conducted in Naresuan University Hospital, Thailand, to compare the saliva microbiome of AIS and TIA stroke patients of Thai ethnic with matched healthy controls. Microbial profiles were analyzed by metagenomics combined 16S rRNA gene sequencing to assess microbial alpha diversity, taxonomic composition, beta diversity, and microbial functional pathways.Forty-one patients (31 AIS and 10 TIA) and 20 age- and sex-matched stroke-free healthy controls were included in this study. Baseline characteristics were comparable between groups, apart from higher rates of hypertension, diabetes, and smoking in the patient group. Patients exhibited significantly higher alpha-diversity genus richness by OTUs and Chao1 index than controls (p < 0.001), highlighting an altered microbial community structure. Phylum-level analysis revealed an increased abundance of Bacillota (p = 0.0285) in the patient group, with a statistically decreasing trend for Bacteroidota, Actinomycetota and Pseudomonadota (p < 0.05). At the genus level, Streptococcus was more significantly abundant in the patients (p = 0.0171), while Prevotella was reduced. The patient and control groups were statistically separated in beta-diversity analysis (PERMANOVA, p < 0.001), with species biomarker analysis by LEfSe (Linear discriminant analysis effect size) could suggest species markers for each group. Functional pathway analysis showed the patient group the significantly higher in functional categories of, for examples, xenobiotics biodegradation and metabolism, cardiovascular diseases, signal transduction, and membrane transport (Welch's t-test, p < 0.05). In conclusion, this study demonstrated the statistical alterations in the saliva microbiome of AIS and TIA patients, characterized by increased genus richness diversity and relatively distinct microbial shifts that may be associated with stroke-related inflammation. The findings suggest the saliva microbiome analysis as potential as a non-invasive biomarker for stroke risk and its role in stroke pathophysiology.

Indexed as

DysbiosisIschemic Attack, TransientIschemic StrokeMicrobiotaMouthAgedBacteriaCase-Control StudiesFemaleHumansMaleMiddle AgedProspective StudiesRNA, Ribosomal, 16SSalivaRNA, Ribosomal, 16S

Identifiers

PMID41056245
PMCPMC12503293

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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.