4.5 Article

MMP-12 and S100s in saliva reflect different aspects of periodontal inflammation

Journal

CYTOKINE
Volume 113, Issue -, Pages 155-161

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.cyto.2018.06.036

Keywords

Saliva; Matrix metalloproteinase 12; Calprotectin; S100A12 protein; Periodontitis; Dental caries

Funding

  1. Regional Board of Dental Public Health in the county of Skane, Sweden
  2. Swedish National Graduate School in Odontological Science
  3. Department of Dental Medicine, Division of Oral Diseases, Karolinska Institutet, Stockholm, Sweden
  4. Swedish Research Council [2012-07110]
  5. Karolinska Institutet
  6. Stockholm County Council
  7. Swedish Patent Revenue Fund for Research in Preventive Odontology
  8. Swedish Dental Society

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Matrix metalloproteinase (MMP)-12, S100A8/A9, and S100Al2 are involved in innate immune responses. We addressed whether different aspects of oral health and non-disease-related covariates influence their levels in saliva. 436 participants were clinically examined, completed a health questionnaire, and provided stimulated saliva. Salivary levels of MMP-12, S100A8/A9, and S100Al2 were determined by enzyme-linked immunosorbent assays. Lower MMP-12 levels were observed in individuals 40-64 years old (yo) compared to < 40 yo, and higher S100A8/A9 levels were found in individuals > 64 yo compared to 40-64 yo. Smokers exhibited lower MMP-12 and S100Al2 levels compared to non-smokers. All three proteins were elevated in individuals with bleeding on probing (BOP) > 20% compared to those with BOP <= 20%, and the S100A8/A9 levels were higher in individuals having >= 10% gingival pocket depths (PPD) >= 4 mm compared to the ones with shallow pockets < 4 mm. The extent of alveolar bone loss or presence of manifest caries did not alter any of the markers. MMP-12, S100A8/A9, and S100A12 levels were higher in participants with high periodontal inflammatory burden. All three proteins correlated positively to BOP, PPD, and to several inflammatory mediators. The explanatory variables for MMP-12 in saliva were age, smoking, presence of any tumor, and percentage of PPD 4 mm. The determinant of salivary S100A8/A9 was percentage of BOP, while S100Al2 levels were associated with percentage of BOP and presence of any tumor. Taken together, MMP-12 and the S100/calgranulin levels in saliva reflect different aspects of periodontal inflammation. Smoking and age should be taken into account in further investigation of these proteins as biomarker candidates of periodontal disease.

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