BMC Oral Health· 2026Q1
Potential causal associations of oral microbiome with rheumatoid arthritis, systemic lupus erythematosus and Sjögren’s disease
- 0citations
- Q1SCImago
- 2026year
Short summary
Genetic predisposition to higher oral abundance of Bacteroidales is causally associated with increased rheumatoid arthritis (RA) risk (OR 1.04, P=0.008), while higher Bacilli abundance is linked to increased Sjögren's disease (SjD) risk (OR 1.08, P=0.032).
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Key points
- Genetic predisposition to higher oral Bacteroidales abundance causally linked to increased RA risk (OR 1.04, P=0.008).
- Higher oral Bacilli abundance associated with increased SjD risk (OR 1.08, P=0.032).
- Oral Pasteurellaceae abundance potentially inversely associated with SjD risk (OR 0.94, P=0.037).
- Reverse Mendelian randomization found no significant association of RA, SLE, or SjD with oral microbiota abundance.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Background This study was to clarify potential bidirectional causal associations between oral microbiome and autoimmune diseases including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE) and Sjögren’s disease (SjD). Methods Two-sample Mendelian randomization (MR) analyses were conducted using summary statistics from genome-wide association study datasets for oral microbiota abundance, RA, SLE and SjD from European participants. Inverse-variance-weighted (IVW), MR-Egger, weighted median, and weighted mode methods were utilized. Multiple testing corrections were implemented using Bonferroni procedure. Results IVW method found that genetic predisposition of order Bacteroidales abundance in oral microbiome was significantly associated with a higher risk of RA (Odds ratio (OR) and 95% Confidence interval (95% CI): 1.04 (1.01, 1.08), P = 0.008, corrected P = 0.033). Furthermore, order Fusobacteriales abundance was positively associated with SLE but species Schaalia abundance was negatively associated with SLE by IVW method (OR and 95% CI: Fusobacteriales: 1.08 (1.01 − 1.17), P = 0.034, corrected P = 0.134; Schaalia: 0.87 (0.80 − 0.95), P = 0.003, corrected P = 0.058). Additionally, class Bacilli abundance in oral microbiome was related with a higher risk of SjD but family Pasteurellaceae in oral microbiome was related with a lower risk of SjD (IVW OR and 95% CI: Bacilli: 1.08 (1.01 − 1.15), P = 0.032, corrected P = 0.032; Pasteurellaceae: 0.94 (0.89 − 0.99), P = 0.037, corrected P = 0.184). Further MR-Egger, weighted median method and weighted mode method and sensitivity MR analyses after excluding confounding SNPs associated with smoking, periodontitis, and dental caries displayed similar trends. However, reverse MR analyses did not find significant associations of RA, SLE and SjD with oral microbiota abundance. Conclusion RA, SLE and SjD may be associated with specific oral bacteria abundance. Bacteroidales may be causally associated with RA. There was suggestive evidence for a positive association between Fusobacteriales and elevated SLE risk and an inverse association between Schaalia and reduced SLE risk. This MR analysis further identified a positive link between Bacilli and SjD but a possible negative link between Pasteurellaceae and SjD. The genetic evidence highlighted the important roles of oral microbiome in autoimmune diseases, although further studies were needed to validate these findings.
The authors' abstract, as published at the source. BMC Oral Health, 2026 · DOI ↗
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Field: Periodontics
PeriodonticsDentistry