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Characterization of the salivary microbiome of adults with inflammatory bowel disease.

作者信息

DeClercq Vanessa, Wright Robyn J, van Limbergen Johan, Langille Morgan G I

机构信息

Department of Pharmacology, Dalhousie University, Halifax, NS, Canada.

Department of Paediatric Gastroenterology and Nutrition, Emma Children's Hospital, Amsterdam UMC, Amsterdam, The Netherlands.

出版信息

J Oral Microbiol. 2025 Apr 30;17(1):2499923. doi: 10.1080/20002297.2025.2499923. eCollection 2025.


DOI:10.1080/20002297.2025.2499923
PMID:40322049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12046613/
Abstract

BACKGROUND: Perturbations of the gut microbiota in patients with inflammatory bowel disease (IBD) have been extensively characterised, but changes to the oral microbiome remain understudied. This study aimed to evaluate the oral microbiome of adults with IBD and of matched controls. METHODS: Saliva samples and data were obtained from a Canadian population cohort ( = 320). The salivary microbiome was characterised using 16S rRNA gene sequencing and examined for differences between control participants and those with IBD, as well as disease subcategories (Crohn's Disease and Ulcerative Colitis). RESULTS: Alpha diversity was significantly lower in participants with IBD than controls in unadjusted models and many remained significant after adjusting for covariates. Significant differences in some beta diversity metrics between participants with IBD and controls were found, although these did not remain significant when adjusted for covariates. Ten genera were significantly differentially abundant between cases and controls. and were both increased in abundance in IBD cases controls (25% 22% and 14% 12%, respectively). CONCLUSION: These results showcase changes in oral microbial diversity and composition in those living with IBD and highlight the potential of using the salivary microbiome as a biomarker for screening or monitoring IBD.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/572f174ec460/ZJOM_A_2499923_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/057c612e0083/ZJOM_A_2499923_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/9db65b74b847/ZJOM_A_2499923_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/572f174ec460/ZJOM_A_2499923_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/057c612e0083/ZJOM_A_2499923_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/9db65b74b847/ZJOM_A_2499923_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b4/12046613/572f174ec460/ZJOM_A_2499923_F0003_OC.jpg

相似文献

[1]
Characterization of the salivary microbiome of adults with inflammatory bowel disease.

J Oral Microbiol. 2025-4-30

[2]
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[3]
Dysbiosis of salivary microbiota in inflammatory bowel disease and its association with oral immunological biomarkers.

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[4]
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[5]
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Inflamm Bowel Dis. 2025-4-25

[6]
Dysbiosis and Ecotypes of the Salivary Microbiome Associated With Inflammatory Bowel Diseases and the Assistance in Diagnosis of Diseases Using Oral Bacterial Profiles.

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[7]
The Fecal Microbiome of IBD Patients Is Less Divertible by Bowel Preparation Compared to Healthy Controls: Results From a Prospective Study.

Inflamm Bowel Dis. 2025-7-7

[8]
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Front Immunol. 2022

[9]
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[10]
Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases.

Inflamm Bowel Dis. 2021-11-15

本文引用的文献

[1]
Is Short-Read 16S rRNA Sequencing of Oral Microbiome Sampling a Suitable Diagnostic Tool for Head and Neck Cancer?

Pathogens. 2024-9-24

[2]
Healthy First-Degree Relatives From Multiplex Families vs Simplex Families Have Higher Subclinical Intestinal Inflammation, a Distinct Fecal Microbial Signature, and Harbor a Higher Risk of Developing Crohn's Disease.

Gastroenterology. 2025-1

[3]
Association Between Healthy Eating Index-2020 and Oral Microbiome Among Postmenopausal Women.

J Nutr. 2025-1

[4]
Environmental Factors Associated With Risk of Crohn's Disease Development in the Crohn's and Colitis Canada - Genetic, Environmental, Microbial Project.

Clin Gastroenterol Hepatol. 2024-9

[5]
Commentary on the Epidemiology of Inflammatory Bowel Disease in Compounding Prevalence Nations: Toward Sustaining Healthcare Delivery.

Gastroenterology. 2024-6

[6]
Global evolving patterns and cross-country inequalities of inflammatory bowel disease burden from 1990 to 2019: a worldwide report.

Inflamm Res. 2024-2

[7]
Multigroup analysis of compositions of microbiomes with covariate adjustments and repeated measures.

Nat Methods. 2024-1

[8]
The Potential Association Between Inflammatory Bowel Diseases and Apical Periodontitis: A Systematic Review and Meta-Analysis.

Eur Endod J. 2024-1-1

[9]
Trends of inflammatory bowel disease from the Global Burden of Disease Study (1990-2019).

Indian J Gastroenterol. 2024-2

[10]
Unraveling the Impact of Gut and Oral Microbiome on Gut Health in Inflammatory Bowel Diseases.

Nutrients. 2023-7-29

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