Evidence map›Paper›PMID 41981895›Full record

ArticleJournal of periodontology2026

Periodontitis during pregnancy: The effect on the gut microbiome and intestinal inflammation.

Richard Bright, Matthew G Macowan, Keyuan Tian, Tracy Fitzsimmons, Rebecca L Wilson, Claire T Roberts, Claus T Christophersen, Peter M Bartold, Stephen P Kidd, Peter S Zilm

Abstract read
In one paragraph

Article in Journal of periodontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

10 authors.

Richard BrightCollege of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.ORCID https://orcid.org/0000-0003-1988-0725
Matthew G MacowanSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-7721-1349
Keyuan TianAdelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.
Tracy FitzsimmonsAdelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-1029-8352
Rebecca L WilsonRobinson Research Institute, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-3867-7784
Claire T RobertsCollege of Medicine and Public Health, Flinders University, Bedford Park, South Australia, Australia.ORCID https://orcid.org/0000-0002-9250-2192
Claus T ChristophersenSchool of Medical and Health Sciences, Edith Cowan University, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0003-1591-5871
Peter M BartoldAdelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-5695-3877
Stephen P KiddSchool of Biological Sciences, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0002-2118-1651
Peter S ZilmAdelaide Dental School, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-7554-9717

Funding

Australian Dental Research Foundation 190-2027
6 · The paper itself

Abstract

backgroundPeriodontitis has been epidemiologically associated with adverse pregnancy outcomes, but causality remains difficult to establish in humans due to confounding factors. This study uses a controlled murine model to examine the effects of experimentally induced periodontitis on the composition of the gut microbiota and gastrointestinal inflammation during pregnancy.

methodsPeriodontitis was induced in pregnant BALB/c mice via oral inoculation with Porphyromonas gingivalis and Fusobacterium nucleatum before conception (n = 20 per group). Pregnancy outcomes, gut histology, systemic inflammatory markers, and microbiome composition, assessed by 16S rRNA sequencing, were evaluated at gestational Day 18.

resultsPeriodontitis was confirmed by significant alveolar bone loss. While fetal and placental weights were modestly increased in periodontitis-positive mice, there were no changes in implantation rates or placental efficiency. Systemic inflammatory markers, including C-reactive protein and interleukin-33, were reduced, suggesting pregnancy-specific immunomodulation. Histological analysis revealed significant inflammation in the jejunum and colon of periodontitis-exposed mice. Despite this, alpha and beta diversity metrics of the gut microbiota remained essentially unchanged. Taxonomic shifts were observed at the genus level, with reductions in protective taxa, such as Akkermansia muciniphila and increases in potentially pro-inflammatory genera, like Desulfovibrio.

conclusionsPeriodontitis during pregnancy alters gut microbial composition and increases gastrointestinal inflammation without overtly impairing pregnancy outcomes in mice. These findings suggest an association between oral inflammation, intestinal inflammatory changes, and systemic inflammatory modulation during pregnancy. Further studies are warranted to explore long-term maternal and offspring consequences and their relevance to human pregnancy. PLAIN LANGUAGE SUMMARY: This study explored how periodontitis during pregnancy can influence the gut and immune system. Periodontitis is already associated with poor pregnancy outcomes, but establishing cause and effect in humans is difficult. To investigate this, the researchers used a controlled mouse model. We induced periodontitis in pregnant mice and examined its impact on the gut microbiome, intestinal health, and immune responses. The results revealed that periodontitis does not stay confined to the mouth; it disrupts gut bacterial balance, causes gut inflammation, and modifies immune pathways. Notably, these effects occurred during pregnancy, a time when the immune system is already adapting. The findings suggest that oral infections during pregnancy can have widespread effects, impacting gut health and immune regulation. This may help explain the link between periodontitis and human pregnancy complications. Overall, the study underscores the importance of oral health during pregnancy and supports the idea that treating periodontitis might also safeguard gut and immune health, leading to better outcomes for both mothers and their babies.

Indexed as

Gastrointestinal MicrobiomePeriodontitisPregnancy ComplicationsAlveolar Bone LossAnimalsDisease Models, AnimalFemaleFusobacterium nucleatumInflammationMiceMice, Inbred BALB CPlacentaPorphyromonas gingivalisPregnancyPregnancy Outcomeadverse pregnancy outcomesgut microbiomeinflammationmicrobiota dysbiosisperiodontitis

Identifiers

PMID41981895
PMCPMC13380379

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Registered trials

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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.