Evidence map›Paper›PMID 41324668›Full record

Observational studySurgery today2026

Periodontitis as a potential predisposing factor for gallstone cholecystitis: exploring the role of chronic systemic inflammation.

Mevlut Yordanagil, Hamdi Taner Turgut, Baris Tuzun, Ercument Helvaci, Ismail Okan

Abstract readObservational Study
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In one paragraph

Observational study in Surgery today, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Mevlut YordanagilDepartment of Surgical Oncology, Kocaeli City Hospital, Kocaeli, Turkey. mevlut.yordanagil@gmail.com.ORCID http://orcid.org/0000-0002-0015-3694
Hamdi Taner TurgutDepartment of General Surgery, Kocaeli City Hospital, Kocaeli, Turkey.
Baris TuzunDepartment of General Surgery, Kocaeli City Hospital, Kocaeli, Turkey.
Ercument HelvaciDepartment of Dentistry, Kocaeli City Hospital, Kocaeli, Turkey.
Ismail OkanFaculty of Medicine, Department of General Surgery, Medeniyet University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePeriodontitis is a chronic oral disease that contributes to low-grade systemic inflammation and may predispose to extraoral complications. We conducted this study to analyze its association with gallstone-related cholecystitis.

methodsThe subjects of this prospective observational study were 160 adults with acute calculous cholecystitis or symptomatic cholelithiasis. The patients were grouped according to their periodontal status as having “normal/mild” or “moderate/severe” peridontitis. We calculated the inflammatory indices: the lymphocyte-to-C-reactive protein ratio (LCR), neutrophil-to-lymphocyte ratio (NLR), derived NLR (d-NLR), and platelet-to-lymphocyte ratio (PLR); and analyzed the associations between periodontal status, inflammatory markers, and gallbladder pathology, using univariate and multivariate models.

resultsModerate/severe periodontitis was found significantly more frequently in patients with cholecystitis than in those with uncomplicated gallstones (80% vs. 22.5%, p < 0.001). Patients with cholecystitis had lower LCR and higher NLR, d-NLR, and PLR values (all p < 0.05). Multivariate analysis identified periodontitis (HR = 1.797) and all inflammatory markers as independent predictors of cholecystitis. Severe periodontitis was especially prevalent in patients with active acute cholecystitis.

conclusionPeriodontitis is significantly associated with acute cholecystitis, potentially through systemic inflammatory mechanisms. Thus, periodontal evaluation may be important in the management and prevention of biliary tract complications.

Indexed as

CholecystitisGallstonesInflammationPeriodontitisAdultAgedBiomarkersBlood PlateletsChronic DiseaseC-Reactive ProteinFemaleHumansInflammation MediatorsLymphocytesMaleMiddle AgedBiomarkersC-Reactive ProteinInflammation MediatorsCholecystitisGallstonesInflammatory biomarkersLymphocyte-to-C-reactive protein ratioNeutrophil-to-lymphocyte ratioPeriodontitisPlatelet-to-lymphocyte ratio.Systemic inflammation

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.