Evidence map›Paper›PMID 42632882›Full record

ArticleBMC oral health2026

Association between self-reported oral health issues and autoimmune diseases: evidence from UK biobank.

Dongwon Yoon, Barbanente Ottavio, Choa Yun, Sun-Young Jung, May A Beydoun, Lenore J Launer, Minkyo Song

Abstract read
In one paragraph

Article in BMC oral health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dongwon YoonLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA. dwyoon@ewha.ac.kr.ORCID 0000-0002-9369-0789
Barbanente OttavioLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Choa YunLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Sun-Young JungLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
May A BeydounLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Lenore J LaunerLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Minkyo SongLaboratory of Epidemiology and Population Sciences, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.

Funding

Autoimmunity and AgingZIAAG000522 · NIA · NATIONAL INSTITUTE ON AGING · PI SONG, MINKYO · 2023 to 2025
$661k
Intramural NIH HHS ZIA AG000522NIA NIH HHS ZIA AG000522
6 · The paper itself

Abstract

backgroundOral microbiome dysbiosis may contribute to autoimmune disease development, but epidemiological evidence linking oral health and autoimmune disease risk is limited.

objectivesTo evaluate the association between self-reported oral health issues by questionnaire-defined as the presence of painful or bleeding gums, mouth ulcers, toothache, dentures, or loose teeth-and the risk of incident autoimmune diseases in the UK Biobank cohort. MATERIALS AND

methodsIndividuals reporting any oral health issues (painful/bleeding gums, mouth ulcers, toothache, dentures, and loose teeth) were classified as any self-reported oral health issues; others as no self-reported oral health issues. We estimated hazard ratios (HRs) and 95% confidence intervals (CIs) for any autoimmune diseases and 39 types of autoimmune diseases using Cox regression models with Bonferroni correction. We investigated associations of the type and number of self-reported oral health issues with autoimmune diseases.

resultsAmong 451,404 participants (mean age: 56.4 years, 54.2% female), any self-reported oral health issues (N = 177,198; 39.3%) were associated with an increased risk of any autoimmune diseases (HR 1.11, 95% CI 1.09-1.14). Painful gums showed the strongest association (HR 1.39, 95% CI 1.31-1.47), followed by mouth ulcers (1.23, 1.18-1.27) and toothache (1.21, 1.15-1.27). Risk increased with the number of self-reported oral health issues (per 1-issue increase: HR 1.09, 95% CI 1.08-1.11, P-trend < 0.001). For specific autoimmune disease, primary biliary cholangitis (HR 1.65, 95% CI 1.24-2.19), rheumatism (1.48, 1.23-1.77), lichen planus (1.35, 1.15-1.57), Sjögren's disease (1.30, 1.11-1.52), pernicious anemia (1.28, 1.12-1.46), rheumatoid arthritis (1.18, 1.12-1.26), and psoriasis (1.16, 1.07-1.26) were identified.

conclusionsSelf-reported oral health issues were associated with an increased risk of incident autoimmune diseases, suggesting that oral health indicators may serve as clinically relevant markers of autoimmune disease risk.

Indexed as

Autoimmune DiseasesMouth DiseasesOral HealthSelf ReportAgedFemaleHumansMaleMiddle AgedRisk FactorsUK BiobankUnited KingdomAutoimmune diseaseImmune-mediated diseaseOral healthOral microbiomeProspective cohort

Identifiers

PMID42632882
PMCPMC13499303

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.