Inflammation Biomarkers of Advanced Disease in Nongingival Tissues of Chronic Periodontitis Patients

Author:

da Costa Thiago Alvares1,Silva Marcelo José Barbosa2,Alves Polyanna Miranda1,Chica Javier Emílio Lazo1,Barcelos Emilio Zorzo3,Giani Max Antonio Alves4,Garlet Gustavo Pompermaier5,da Silva João Santana6,Rodrigues Júnior Virmondes1,Rodrigues Denise Bertulucci Rocha47,Cardoso Cristina Ribeiro de Barros18

Affiliation:

1. Instituto de Ciências Biológicas e Naturais, Universidade Federal do Triângulo Mineiro, Uberaba, MG, Brazil

2. Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, Uberlândia, MG, Brazil

3. Instituto de Ciências Tecnológicas e Exatas, Universidade Federal do Triângulo Mineiro, Uberaba, MG, Brazil

4. Departamento de Odontologia Clínica, Universidade de Uberaba, Uberaba, MG, Brazil

5. Departamento de Biologia Oral, Faculdade de Odontologia de Bauru, Universidade de São Paulo, Bauru, SP, Brazil

6. Departamento de Bioquímica e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil

7. CEFORES, Universidade Federal do Triângulo Mineiro, Uberaba, MG, Brazil

8. School of Pharmaceutical Sciences of Ribeirão Preto, Department of Clinical Analyzes, Toxicology and Food Sciences, USP, Avenida do Café, s/n, 14040-903 Ribeirão Preto, SP, Brazil

Abstract

Chronic periodontitis is a multifactorial inflammatory disease that affects supporting structures of the teeth. Although the gingival response is largely described, little is known about the immune changes in the alveolar bone and neighboring tissues that could indicate periodontal disease (PD) activity. Then, in this study we identified the ongoing inflammatory changes and novel biomarkers for periodontitis in the tissues directly affected by the destructive disease in PD patients. Samples were collected by osteotomy in 17 control subjects during extraction of third molars and 18 patients with advanced PD, in which alveoloplasty was necessary after extraction of teeth with previous extensive periodontal damage. Patients presented mononuclear cells infiltration in the connective tissue next to the bone and higher fibrosis area, along with increased accumulation of IL-17+and TRAP+cells. The levels of TNF-αand MMP-2 mRNA were also elevated compared to controls and a positive and significant correlation was observed between TNF-αand MMP-2 mRNA expression, considering all samples evaluated. In conclusion, nongingival tissues neighboring large periodontal pockets present inflammatory markers that could predict ongoing bone resorption and disease spreading. Therefore, we suggested that the detailed evaluation of these regions could be of great importance to the assessment of disease progression.

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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