Evidence map›Paper›PMID 39447062›Full record

Observational studyJournal of Crohn's & colitis2025

The Bidirectional Effects of Periodontal Disease and Oral Dysbiosis on Gut Inflammation in Inflammatory Bowel Disease.

Netanel F Zilberstein, Phillip A Engen, Garth R Swanson, Ankur Naqib, Zoe Post, Julian Alutto, Stefan J Green, Maliha Shaikh, Kristi Lawrence, Darbaz Adnan and 4 more

Abstract readObservational Study
In one paragraph

Observational study in Journal of Crohn's & colitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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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

14 authors.

Netanel F ZilbersteinDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Phillip A EngenRush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Rush Medical College, Chicago, IL, USA.ORCID 0000-0002-5276-5174
Garth R SwansonDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Ankur NaqibRush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Rush Medical College, Chicago, IL, USA.
Zoe PostDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Julian AluttoDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Stefan J GreenDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Maliha ShaikhRush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Rush Medical College, Chicago, IL, USA.
Kristi LawrenceRush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Rush Medical College, Chicago, IL, USA.
Darbaz AdnanRush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Rush Medical College, Chicago, IL, USA.
Lijuan ZhangDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Robin M VoigtDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.
Joel SchwartzDepartment of Oral Medicine and Diagnostic Sciences, University of Illinois Chicago, Chicago, IL, USA.
Ali KeshavarzianDepartment of Internal Medicine, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0002-7969-3369

Funding

J. NRSA Training CoreTL1TR002388 · NCATS · UNIVERSITY OF CHICAGO · PI ALI KESHAVARZIAN, Sonia Kupfer · 2017 to 2026
$6.7M
Center for Circadian Rhythms and Alcohol-Induced Tissue DamageR24AA026801 · NIAAA · RUSH UNIVERSITY MEDICAL CENTER · PI ALI KESHAVARZIAN · 2019 to 2026
$4.5M
NCATS NIH HHS 2TL1TR002388-06NCATS NIH HHS TL1 TR002388NIAAA NIH HHS R24 AA026801NIAAA NIH HHS R24AA026801
6 · The paper itself

Abstract

BACKGROUND AND

aimsInflammatory bowel disease (IBD) flares can lead to excessive morbidity and mortality. This study aimed to determine whether oral dysbiosis/periodontal disease (PD) is common in IBD and is associated with disease activity in IBD.

methodsThis single-center, prospective, cross-sectional, proof-of-concept, and observational study assessed the frequency of periodontal inflammatory disease and interrogated oral and stool microbiota using 16S rRNA gene amplicon sequencing of active-IBD (aIBD), inactive-IBD (iIBD), and healthy controls (HC). Questionnaires assessed diet, alcohol usage, oral hygiene behavior, and disease activity. A subset of participants underwent comprehensive dental examinations to evaluate PD.

resultsPeriodontal disease was severer in aIBD subjects than in HC, as aIBD had poorer quality diets (lower Mediterranean diet scores) than iIBD and HC. Significant differences in microbial community structure were observed in unstimulated saliva, stimulated saliva, gingiva, and stool samples, primarily between aIBD and HC. Saliva from aIBD had higher relative abundances of putative oral pathobionts from the genera Streptococcus, Granulicatella, Rothia, and Actinomyces relative to HC, despite similar oral hygiene behaviors between groups.

conclusionsOur study suggests that patients with aIBD have severer periodontal disorders and higher relative abundances of putative 'pro-inflammatory' microbiota in their oral cavity, despite normal oral hygiene behaviors. Our data are consistent with the potential presence of an oral-gut inflammatory axis that could trigger IBD flare-ups in at-risk patients. Routine dental health assessments in all IBD patients should be encouraged as part of the health maintenance of IBD and as a potential strategy to decrease the risk of IBD flares.

Indexed as

DysbiosisInflammatory Bowel DiseasesPeriodontal DiseasesAdultCase-Control StudiesCross-Sectional StudiesFecesFemaleGastrointestinal MicrobiomeHumansMaleMiddle AgedMouthOral HygieneProspective StudiesRNA, Ribosomal, 16SRNA, Ribosomal, 16Sdysbiosisinflammatory bowel diseasemicrobiotaoral hygieneperiodontal disease

Identifiers

PMID39447062
PMCPMC12041420

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.