Evidence map›Paper›PMID 37316411›Full record

ArticleInternational dental journal2023

Loricrin and Cytokeratin Disorganisation in Severe Forms of Periodontitis.

Raisa Queiroz Catunda, Karen Ka-Yan Ho, Srushti Patel, Christopher Bryant Roy, Maria Alexiou, Liran Levin, Benjamin J Ulrich, Mark H Kaplan, Maria Febbraio

Open access · goldAbstract read
In one paragraph

Article in International dental journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 90% 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.

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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
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

9 authors at 3 institutions in 2 countries.

Raisa Queiroz CatundaDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Karen Ka-Yan HoDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Srushti PatelDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Christopher Bryant RoyDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Maria AlexiouDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Liran LevinDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada.
Benjamin J UlrichNorthwestern University, Chicago, Illinois, USA.
Mark H KaplanDepartment of Microbiology & Immunology, School of Medicine, Indiana University, Indianapolis, Indiana, USA.
Maria FebbraioDepartment of Dentistry, College of Health Sciences, University of Alberta, Edmonton, Alberta, Canada. Electronic address: febbraio@ualberta.ca.
University of Alberta · CAIndiana University – Purdue University Indianapolis · USNorthwestern University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this research was to investigate the role of the cornified epithelium, the outermost layer of the oral mucosa, engineered to prevent water loss and microorganism invasion, in severe forms of periodontitis (stage III or IV, grade C).

methodsPorphyromonas gingivalis, a major periodontal disease pathogen, can affect cornified epithelial protein expression through chronic activation of signal transducer and activator of transcription 6 (Stat6). We used a mouse model, Stat6VT, that mimics this to determine the effects of barrier defect on P gingivalis-induced inflammation, bone loss, and cornified epithelial protein expression, and compared histologic and immunohistologic findings with tissues obtained from human controls and patients with stage III and IV, grade C disease. Alveolar bone loss in mice was assessed using micro-computerised tomography, and soft tissue morphology was qualitatively and semi-quantitatively assessed by histologic examination for several proteins, including loricrin, filaggrin, cytokeratin 1, cytokeratin 14, a proliferation marker, a pan-leukocyte marker, as well as morphologic signs of inflammation. Relative cytokine levels were measured in mouse plasma by cytokine array.

resultsIn the tissues from patients with periodontal disease, there were greater signs of inflammation (rete pegs, clear cells, inflammatory infiltrates) and a decrease and broadening of expression of loricrin and cytokeratin 1. Cytokeratin 14 expression was also broader and decreased in stage IV. P gingivalis-infected Stat6VT mice showed greater alveolar bone loss in 9 out of 16 examined sites, and similar patterns of disruption to human patients in expression of loricrin and cytokeratins 1 and 14. There were also increased numbers of leukocytes, decreased proliferation, and greater signs of inflammation compared with P gingivalis-infected control mice.

conclusionsOur study provides evidence that changes in epithelial organisation can exacerbate the effects of P gingivalis infection, with similarities to the most severe forms of human periodontitis.

Indexed as

Alveolar Bone LossPeriodontitisAnimalsCytokinesHumansInflammationKeratin-14KeratinsMembrane ProteinsMicePorphyromonas gingivalisCytokinesKeratin-14KeratinsloricrinMembrane ProteinsEpithelial barrierLoricrinPeriodontal diseaseStat6VT

Identifiers

PMID37316411
PMCPMC10658443
OpenAlexW4380356502

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.