Causal Association Analysis of Periodontitis and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study
- PMID: 38408068
- PMCID: PMC11291616
- DOI: 10.1093/ibd/izad188
Causal Association Analysis of Periodontitis and Inflammatory Bowel Disease: A Bidirectional Mendelian Randomization Study
Abstract
Background: Periodontitis has been reported to be associated with inflammatory bowel disease (IBD), including ulcerative colitis (UC), and Crohn's disease (CD). However, the causality of these 2 diseases remains unclear. We conducted bidirectional Mendelian randomization (MR) to investigate the causal relationship between periodontitis and IBD.
Methods: We obtained the genome-wide association study (GWAS) summary data of European populations from FinnGen database (for IBD) and a published article (for periodontitis), from which independent single nucleotide polymorphisms were selected as instrumental variables. Inverse variance-weighted (IVW), MR-Egger, and weighted median (WM) methods were utilized for MR analysis. Heterogeneity or pleiotropy was detected through Cochran's Q test and MR-Egger intercept, respectively. Outlier was identified with MR-PRESSO (Mendelian Randomization Pleiotropy RESidual Sum and Outlier) and leave-one-out analysis. All statistical analyses were performed with R 4.2.1 and the packages of TwoSampleMR version 0.5.6.
Results: Genetic prediction showed that periodontitis was the risk factor of UC (odds ratio [OR], 1.13; 95% confidence interval [CI], 1.01-1.26; P = .027), rather than of CD (OR, 0.92; 95% CI, 0.74-1.15; P = .456) and IBD (OR, 0.96; 95% CI, 0.81-1.13; P = .619). To the contrary, CD, not UC or IBD, resulted in exacerbating periodontitis in terms of the results of the IVW (OR, 1.09; 95% CI, 1.01-1.17; P = .021) and WM (OR, 1.10; 95% CI, 1.01-1.20; P = .030) methods. Heterogeneity or pleiotropy was acceptable.
Conclusions: Our results indicated that CD was the risk factor for periodontitis; conversely, periodontitis was responsible for the exacerbation of UC, enhancing the existence of mouth-gut axis. Patients with UC should pay more attention to periodontal health, while patients with periodontitis should actively pay close heed to intestinal health.
Keywords: IBD; Mendelian randomization; causal relationship; periodontitis.
Plain language summary
A bidirectional Mendelian randomization study indicated that Crohn’s disease was the risk factor for periodontitis; conversely, periodontitis was responsible for the exacerbation of ulcerative colitis, enhancing the existence of the mouth-gut axis and suggesting paying attention to oral health for patients of inflammatory bowel disease.
© 2024 Crohn’s & Colitis Foundation. Published by Oxford University Press on behalf of Crohn’s & Colitis Foundation.
Conflict of interest statement
All authors declare no conflicts of interest.
Figures
Similar articles
-
Unraveling the link between inflammatory bowel disease and perianal abscess: insights from bidirectional and multivariable Mendelian randomization study.BMC Gastroenterol. 2025 Jul 29;25(1):538. doi: 10.1186/s12876-025-04137-x. BMC Gastroenterol. 2025. PMID: 40730952 Free PMC article.
-
Causality of inflammatory bowel disease and seborrheic keratosis: A bidirectional two-sample Mendelian randomization study.Skin Res Technol. 2024 Aug;30(8):e13876. doi: 10.1111/srt.13876. Skin Res Technol. 2024. PMID: 39081143 Free PMC article.
-
Ischemic Stroke May Increase the Risk of Crohn's Disease and Ulcerative Colitis: Evidence from a Bidirectional Mendelian Randomization Study.World Neurosurg. 2025 Apr;196:123718. doi: 10.1016/j.wneu.2025.123718. Epub 2025 Mar 13. World Neurosurg. 2025. PMID: 39929265
-
A systematic review and network meta-analysis of the association between periodontitis and inflammatory bowel diseases.BMC Oral Health. 2025 Mar 31;25(1):463. doi: 10.1186/s12903-025-05830-9. BMC Oral Health. 2025. PMID: 40165211 Free PMC article.
-
Risk of stroke in patients with inflammatory bowel disease: a systematic review and meta-analysis.BMC Gastroenterol. 2025 Feb 25;25(1):114. doi: 10.1186/s12876-025-03702-8. BMC Gastroenterol. 2025. PMID: 40000943 Free PMC article.
Cited by
-
Association of 41 Inflammatory Cytokines With Common Oral Diseases.Int Dent J. 2025 Apr;75(2):683-691. doi: 10.1016/j.identj.2024.10.025. Epub 2024 Dec 18. Int Dent J. 2025. PMID: 39694712 Free PMC article.
-
Immune-Mediated Bidirectional Causality Between Inflammatory Bowel Disease and Chronic Periodontitis: Evidence from Mendelian Randomization and Integrative Bioinformatics Analysis.Biomedicines. 2025 Feb 15;13(2):476. doi: 10.3390/biomedicines13020476. Biomedicines. 2025. PMID: 40002889 Free PMC article.
References
-
- Kobayashi T, Siegmund B, Le Berre C, et al. Ulcerative colitis. Nat Rev Dis Primers. 2020;6(1):74. - PubMed
-
- Roda G, Chien NGS, Kotze PG, et al. Crohn’s disease. Nat Rev Dis Primers. 2020;6(1):22. - PubMed
-
- Zhao M, Gönczi L, Lakatos PL, Burisch J.. The burden of inflammatory bowel disease in Europe in 2020. J Crohns Colitis 2021;15(9):1573-1587. - PubMed
-
- Bancil AS, Sandall AM, Rossi M, Chassaing B, Lindsay JO, Whelan K.. Food additive emulsifiers and their impact on gut microbiome, permeability, and inflammation: mechanistic insights in inflammatory bowel disease. J Crohns Colitis 2021;15(6):1068-1079. - PubMed
-
- Lerner A, Matthias T.. Changes in intestinal tight junction permeability associated with industrial food additives explain the rising incidence of autoimmune disease. Autoimmun Rev. 2015;14(6):479-489. - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Medical