Evidence map›Paper›PMID 39462428›Full record

Trial reportMicrobiome2024

The role of the oral microbiota in the causal effect of adjunctive antibiotics on clinical outcomes in stage III-IV periodontitis patients.

Sven Kleine Bardenhorst, Daniel Hagenfeld, Johannes Matern, Karola Prior, Inga Harks, Peter Eickholz, Katrin Lorenz, Ti-Sun Kim, Thomas Kocher, Jörg Meyle and 4 more

Erratum issuedAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Effects of Non-Surgical Periodontal Therapy on Dental Plaque Microbiome.International journal of molecular sciences · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Sven Kleine Bardenhorst *Department of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.
Daniel Hagenfeld *Department of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany. daniel.hagenfeld@ukmuenster.de.
Johannes MaternDepartment of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.
Karola PriorDepartment of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.
Inga HarksDepartment of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.
Peter EickholzDepartment of Periodontology, Center for Dentistry and Oral Medicine, Goethe University Frankfurt, Frankfurt, Germany.
Katrin LorenzDepartment of Periodontology, TU Dresden, Dresden, Germany.
Ti-Sun KimDepartment of Conservative Dentistry, Section of Periodontology, Clinic for Oral, Dental and Maxillofacial Diseases, Heidelberg University Hospital, Heidelberg, Germany.
Thomas KocherDepartment of Restorative Dentistry, Periodontology, Endodontology, and Preventive and Pediatric Dentistry, University Medicine Greifswald, Greifswald, Germany.
Jörg MeyleDepartment of Periodontology, University of Giessen, Giessen, Germany.
Doğan KanerDepartments of Periodontology and Synoptic Dentistry, Charite-Universitätsmedizin Berlin, Berlin, Germany.
Yvonne Jockel-SchneiderDepartment of Periodontology, University Hospital Würzburg, Würzburg, Germany.
Dag HarmsenDepartment of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.
Benjamin EhmkeDepartment of Periodontology and Operative Dentistry, Muenster University Hospital, Albert-Schweitzer-Campus 1, Building W30, Münster, 48149, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeriodontitis, a prevalent chronic inflammatory disease, offers insights into the broader landscape of chronic inflammatory conditions. The progression and treatment outcomes of periodontitis are closely related to the oral microbiota's composition. Adjunctive systemic Amoxicillin 500 mg and Metronidazole 400 mg, often prescribed thrice daily for 7 days to enhance periodontal therapy's efficacy, have lasting effects on the oral microbiome. However, the precise mechanism through which the oral microbiome influences clinical outcomes in periodontitis patients remains debated. This investigation explores the pivotal role of the oral microbiome's composition in mediating the outcomes of adjunctive systemic antibiotic treatment.

methodsSubgingival plaque samples from 10 periodontally healthy and 163 periodontitis patients from a randomized clinical trial on periodontal therapy were analyzed. Patients received either adjunctive amoxicillin/metronidazole or a placebo after mechanical periodontal treatment. Microbial samples were collected at various intervals up to 26 months post-therapy. Using topic models, we identified microbial communities associated with normobiotic and dysbiotic states, validated with 86 external and 40 internal samples. Logistic regression models evaluated the association between these microbial communities and clinical periodontitis parameters. A Directed Acyclic Graph (DAG) determined the mediating role of oral microbiota in the causal path of antibiotic treatment effects on clinical outcomes.

resultsWe identified clear distinctions between dysbiotic and normobiotic microbial communities, differentiating healthy from periodontitis subjects. Dysbiotic states consistently associated with below median %Pocket Probing Depth ≥ 5 mm (OR = 1.26, 95% CI [1.14-1.42]) and %Bleeding on Probing (OR = 1.09, 95% CI [1.00-1.18]). Factors like microbial response to treatment, smoking, and age were predictors of clinical attachment loss progression, whereas sex and antibiotic treatment were not. Further, we showed that the oral microbial treatment response plays a crucial role in the causal effect of antibiotic treatment on clinical treatment outcomes.

conclusionsThe shift towards a normobiotic subgingival microbiome, primarily induced by adjunctive antibiotics, underscores the potential for microbiome-targeted interventions to enhance therapeutic efficacy in chronic inflammatory conditions. This study reaffirms the importance of understanding the oral microbiome's role in periodontal health and paves the way for future research exploring personalized treatment strategies based on individual microbiome profiles. Video Abstract.

Indexed as

AmoxicillinAnti-Bacterial AgentsMetronidazoleMicrobiotaPeriodontitisAdultBacteriaDental PlaqueDysbiosisFemaleHumansMaleMiddle AgedMouthTreatment OutcomeAmoxicillinAnti-Bacterial AgentsMetronidazoleAntibiotic treatmentClinical attachment lossClinical outcomesDirected acyclic graphsDysbiosisMicrobial communitiesNormobioticOral microbiotaPeriodontitisSubgingival plaque

Identifiers

PMID39462428
PMCPMC11515798

What OpenQuestion holds

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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.