Evidence map›Paper›PMID 37814163›Full record

ArticleClinical oral investigations2023

Wnt signaling in periodontitis.

Zeliha Güney, Şivge Kurgan, Canan Önder, Mahmure Ayşe Tayman, Ömer Günhan, Alpdoğan Kantarci, Muhittin Abdulkadir Serdar, Meral Günhan

Registry-linked trialAbstract read
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In one paragraph

Article in Clinical oral investigations, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06933784 (Expression of Wnt5a and WNT Coreceptor), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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.

NCT06933784 completednot on this mapstarted 2024, after this paper: background citation

Expression of Wnt5a and WNT Coreceptor (LRP5) Levels in Stage III Periodontitis Patients

Typeobservational_patient_registrySponsorAnkara UniversityRan2024 to 2025Enrolled40ConditionsPeriodontal Disease, Periodontitis (Stage 3), Periodontitis Stage III
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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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

8 authors at 5 institutions in 1 country.

Zeliha GüneyFaculty of Dentistry Department of Periodontology, Ankara University, 06500-Cankaya, Ankara, Turkey.
Şivge KurganFaculty of Dentistry Department of Periodontology, Ankara University, 06500-Cankaya, Ankara, Turkey. sivgeakgun@gmail.com.
Canan ÖnderFaculty of Dentistry Department of Periodontology, Ankara University, 06500-Cankaya, Ankara, Turkey.
Mahmure Ayşe TaymanFaculty of Dentistry Department of Periodontology, Yildirim Beyazit University, Ankara, Turkey.
Ömer GünhanFaculty of Medicine Department of Pathology, TOBB University, Ankara, Turkey.
Alpdoğan KantarciThe Forsyth Institute, Cambridge, MA, USA.
Muhittin Abdulkadir SerdarFaculty of Medicine, Department of Biochemistry, Acibadem University, Istanbul, Turkey.
Meral GünhanFaculty of Dentistry Department of Periodontology, Ankara University, 06500-Cankaya, Ankara, Turkey.
Ankara University · TRAcıbadem University · TRAnkara Medipol ÜniversitesiAnkara Yıldırım Beyazıt University · TRTOBB University of Economics and Technology · TR

Funding

Ankara University Scientific Research Projects Office 17H0234001
6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the Wnt/β-catenin signaling pathway activity in gingival samples obtained from patients with periodontitis. MATERIALS AND

methodsFifteen patients with stage III grade B (SIIIGB) and eleven with stage III grade C (SIIIGC) periodontitis were included and compared to 15 control subjects. β-Catenin, Wnt 3a, Wnt 5a, and Wnt 10b expressions were evaluated by Q-PCR. Topographic localization of tissue β-catenin, Wnt 5a, and Wnt 10b was measured by immunohistochemical analysis. TNF-α was used to assess the inflammatory state of the tissues, while Runx2 was used as a mediator of active destruction.

resultsWnt 3a, Wnt 5a, and Wnt 10b were significantly higher in gingival tissues in both grades of stage 3 periodontitis compared to the control group (p < 0.05). β-Catenin showed intranuclear staining in connective tissue in periodontitis, while it was confined to intracytoplasmic staining in epithelial tissue and the cell walls in the control group. Wnt5a protein expression was elevated in periodontitis, with the most intense staining observed in the connective tissue of SIIIGC samples. Wnt10b showed the highest density in the connective tissue of patients with periodontitis.

conclusionsOur findings suggested that periodontal inflammation disrupts the Wnt/β-catenin signaling pathway. CLINICAL RELEVANCE: Periodontitis disrupts Wnt signaling in periodontal tissues in parallel with tissue inflammation and changes in morphology. This change in Wnt-related signaling pathways that regulate tissue homeostasis in the immunoinflammatory response may shed light on host-induced tissue destruction in the pathogenesis of the periodontal disease.

Indexed as

PeriodontitisWnt Signaling Pathwaybeta CateninGingivaHumansInflammationbeta CateninPeriodontitisWnt 10bWnt 3aWnt 5aβ-Catenin

Identifiers

PMID37814163
OpenAlexW4387444056

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

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.