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Treatment of periodontitis reduces systemic inflammation in type 2 diabetes

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dc.contributor.author Philip, M. Preshaw
dc.contributor.author John, J. Taylor
dc.contributor.author Katrin, M. Jaedicke
dc.contributor.author Marko, De Jager
dc.contributor.author Jan, Willem Bikker
dc.contributor.author Wieke, Selten
dc.contributor.author Susan, M. Bissett
dc.contributor.author Kerry, M. Whall
dc.contributor.author Rachel, van de Merwe
dc.contributor.author Aisha, Areibi
dc.contributor.author Paiboon, Jitprasertwong
dc.contributor.author Rana, Al-Shahwani
dc.contributor.author Jolanta, Weaver
dc.contributor.author Roy, Taylor
dc.contributor.author Rebecca, R. Wassall
dc.date.accessioned 2025-05-11T08:15:27Z
dc.date.available 2025-05-11T08:15:27Z
dc.date.issued 2020
dc.identifier.uri https://repository.uob.edu.ly/handle/123456789/2094
dc.description.abstract Aims: To assess the impact of periodontal treatment on systemic inflammation in type 2 diabetes. Materials and Methods: Adults with type 2 diabetes (n = 83) and without diabetes (controls, n = 75) were recruited, and participants with periodontitis received periodontal treatment and 12 months’ follow-up. Biomarkers for periodontal inflammation (gingival crevicular fluid interleukin-6, tumour necrosis factor-α, interleukin-1β, interferon-γ, matrix metalloproteinase-8, matrix metalloproteinase-9, adiponectin) and serum markers of inflammation and diabetes control (glycated haemoglobin, high sensitivity C-reactive protein, interleukin-6, tumour necrosis factor-α, interleukin-1β, interferon-γ, leptin, adiponectin) were measured. Structural equation modelling was used to evaluate periodontal treatment effects on oral and systemic inflammation. Results: Periodontal treatment resulted in significant improvements in clinical status and reductions in gingival crevicular fluid biomarkers from baseline to month 12. Structural equation modelling identified that, at baseline, individuals with diabetes and periodontitis had significantly higher systemic inflammation than non-diabetic controls with periodontitis (Δ = 0.20, p = .002), with no significant differences between groups for oral inflammation. There was a greater reduction in systemic inflammation following periodontal treatment in individuals with diabetes and periodontitis compared to those with periodontitis but not diabetes (Δ = −0.25, p = .01). Conclusions: Diabetes and periodontitis together appear to increase systemic inflammation, with evidence of reductions following periodontal treatment. en_US
dc.language.iso en en_US
dc.publisher Benghazi University en_US
dc.subject inflammation, periodontitis, diabetes mellitus, type 2 en_US
dc.title Treatment of periodontitis reduces systemic inflammation in type 2 diabetes en_US
dc.type Working Paper en_US


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