ORIGINAL RESEARCH article
Front. Immunol.
Sec. Molecular Innate Immunity
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1668277
This article is part of the Research TopicDevelopment of Diagnostic and Therapeutic Biomarkers for Tumors and Inflammation Based on Multi-omics Approaches Including Transcriptomics, Proteomics, and MetabolomicsView all 3 articles
Shared immune-inflammatory mechanisms between ulcerative colitis and periodontitis: a multi-omics analysis
Provisionally accepted- 1Shanxi Provincial People's Hospital, Taiyuan, China
- 2The First Hospital of Hebei Medical University, Shijiazhuang, China
- 3The Second Hospital of Hebei Medical University, Shijiazhuang, China
Select one of your emails
You have multiple emails registered with Frontiers:
Notify me on publication
Please enter your email address:
If you already have an account, please login
You don't have a Frontiers account ? You can register here
Ulcerative colitis (UC) and periodontitis (PD) are chronic inflammatory diseases with increasing evidence of bidirectional communication through the oral-gut axis. However, the immunological mechanisms underlying their co-occurrence remain largely unclear.We conducted a bidirectional Mendelian randomization (MR) analysis to evaluate potential causal relationships between UC and PD. Transcriptomic data from public repositories were integrated to identify shared differentially expressed genes. Immune-related genes were further screened using three machine learning approaches. Enrichment analysis and immune cell infiltration profiling were performed to explore underlying mechanisms. A rat model combining UC and PD was established to validate key findings in vivo.MR analysis revealed a unidirectional causal effect of UC on PD. Among the intersected immunerelated genes, CXCL6 was identified as a hub gene significantly upregulated in both UC and PD. It was associated with neutrophil infiltration and pathways related to chemokine signaling and mucosal barrier disruption. In a dual-disease rat model, CXCL6 expression was further elevated in colonic tissues compared to UC alone, aligning with aggravated epithelial damage.Our study identifies a shared immune signature between UC and PD, highlighting CXCL6 as a pivotal mediator. These insights deepen understanding of oral-gut mucosal interactions and inform future biomarker and mechanistic studies.
Keywords: ulcerative colitis, Periodontitis, CXCL6, oral-gut axis, Mendelian randomization, Immune infiltration
Received: 17 Jul 2025; Accepted: 15 Aug 2025.
Copyright: © 2025 Li, Li, Guo, Zhou, Ma and Gao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Yan Zhou, The First Hospital of Hebei Medical University, Shijiazhuang, China
Shaowei Ma, The Second Hospital of Hebei Medical University, Shijiazhuang, China
Xin Gao, Shanxi Provincial People's Hospital, Taiyuan, China
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.