Are periodontitis and psoriasis associated? A pre‐clinical murine model

Author:

Marruganti Crystal12ORCID,Gaeta Carlo1,Falciani Chiara3,Cinotti Elisa4,Rubegni Pietro4,Alovisi Mario5,Scotti Nicola5,Baldi Andrea5,Bellan Cristiana6,Defraia Chiara6,Fiorino Fabio78,Valensin Silvia9,Bellini Erika9,De Rosa Antonella9,D'Aiuto Francesco2ORCID,Grandini Simone1

Affiliation:

1. Unit of Periodontology, Endodontology and Restorative Dentistry, Department of Medical Biotechnologies University of Siena Siena Italy

2. Periodontology Unit UCL Eastman Dental Institute and Hospital, University College London London UK

3. Department of Medical Biotechnologies University of Siena Siena Italy

4. Unit of Dermatology, Department of Medical, Surgical and Neurological Science University of Siena Siena Italy

5. Department of Surgical Sciences C.I.R. Dental School, University of Turin Turin Italy

6. Unit of Anatomical Pathology, Department of Human Pathology and Oncology University of Siena Siena Italy

7. Laboratory of Molecular Microbiology and Biotechnology (LAMMB), Department of Medical Biotechnologies University of Siena Siena Italy

8. LUM University “Giuseppe Degennaro”, Casamassima (Bari)

9. Fondazione Toscana Life Sciences Siena Italy

Abstract

AbstractAimTo investigate the bidirectional influence between periodontitis and psoriasis, using the respective experimental models of ligature‐ and imiquimod‐induced diseases on murine models.Materials and MethodsThirty‐two C57/BL6J mice were randomly allocated to four experimental groups: control (P− Pso−), ligature‐induced periodontitis (P+ Pso−), imiquimod‐induced psoriasis (P− Pso+) and periodontitis and psoriasis (P+ Pso+). Samples (maxilla, dorsal skin and blood) were harvested immediately after death. Measures of periodontitis (distance between the cemento‐enamel junction and alveolar bone crest [CEJ–ABC] and the number of osteoclasts) and psoriasis (epidermal thickness and infiltrate cell [/0.03mm2]) severity as well as systemic inflammation (IL‐6, IL‐17A, TNF‐α) were collected.ResultsThe P+ Pso+ group exhibited the most severe experimental periodontitis and psoriasis, with the highest values of CEJ–ABC, number of osteoclasts, epidermal thickness and infiltrate cells in the dorsal skin, as well as the highest blood cytokine concentration. The P+ Pso− group presented with higher cell infiltrate (/0.03mm2) compared to the control group (p <.05), while the P− Pso+ group showed substantially higher alveolar bone loss (CEJ–ABC) than the control group (p <.05).ConclusionsExperimental periodontitis may initiate and maintain psoriasiform skin inflammation and, vice versa, experimental psoriasis may contribute to the onset of periodontitis. In a combined model of the diseases, we propose a bidirectional association between periodontitis and psoriasis via systemic inflammation.

Publisher

Wiley

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