4.5 Article

Competing interplay between systemic and periodontal inflammation: obesity overrides the impact of oral periphery

Journal

CLINICAL ORAL INVESTIGATIONS
Volume 25, Issue 4, Pages 2045-2053

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00784-020-03514-y

Keywords

Obesity; Periodontitis; Inflammation; C-reactive protein

Funding

  1. Federal State of Mecklenburg-West Pomerania, Germany

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This study investigated the interaction between local inflammation, periodontitis, and obesity, and found that probing depth and plaque were positively associated with C-reactive protein. Adjusting for waist circumference attenuated the association between probing depth and CRP, but did not eliminate it, with similar findings for plaque.
Objectives We aimed at investigating whether the interaction between the local inflammation, periodontitis, and obesity is independently associated with systemic inflammation. Methods From the population-based Study of Health in Pomerania, 3366 participants, without (2366) and with (1000) obesity, were studied for the association of periodontitis, measured as probing depth (PD) and plaque together with body mass index (BMI) on C-reactive protein (CRP). Quantile regression was used to evaluate the association between periodontal, anthropometric, and inflammatory variables (outcomes). Results The overall prevalence of obesity in this adult population was 31.4% in men and 28.1% in women. Both PD and plaque were positively associated with CRP, revealing an increasing impact across the CRP concentration distribution. Adjusting the regression of CRP or fibrinogen on PD for waist circumference attenuated but did not abolish the PD coefficients. Dental plaque was similarly associated with these interrelations. Association between PD and a dental plaque was different among participants with low-, medium-, or high-risk CRP concentrations. Conclusion Local and systemic sources of inflammation contribute to blood levels of inflammatory markers. The respective contributions depend on the relative rate in each of the inflammation-inducing risks and are dominated by adiposity.

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