Expression of immune-inflammatory markers in sites of chronic periodontitis in patients with type 2 diabetes

J Periodontol. 2012 Apr;83(4):426-34. doi: 10.1902/jop.2011.110324. Epub 2011 Aug 22.

Abstract

Background: The aim of this study is to evaluate the gene expression of immune-inflammatory markers in gingival biopsies of patients with type 2 diabetes with chronic periodontitis (CP).

Methods: Gingival biopsies were harvested from systemically and periodontally healthy patients (SPH), systemically healthy patients with CP (SHCP), and patients with better-controlled and poorly controlled diabetes and CP. The levels of mRNA of interleukin (IL)-17, IL-6, IL-23, IL-10, IL-4, interferon-γ, toll-like receptor (TLR)-2, TLR-4, osteoprotegerin, receptor activator of nuclear factor-kappa B ligand (RANKL), tumor necrosis factor-α, transforming growth factor-β, transcription factor forkhead box p3, transcription factor orphan nuclear receptor C2 (RORC2), and receptor of advanced glycation end products (RAGE) were evaluated by quantitative real-time polymerase chain reaction.

Results: All CP groups presented higher levels of mRNA of TLR-2, TLR-4, IL-17, RANKL, and RAGE and a higher frequency of IL-17 and TLR-2 mRNA-positive biopsies when compared to SPH (P <0.05). There was a higher frequency of detection of RORC2 in the biopsies from both groups with diabetes compared to the other groups (P <0.05). The frequency of IL-4 mRNA-positive tissues was lower in patients with diabetes compared to SHCP (P <0.05).

Conclusion: CP, but not type 2 diabetes mellitus, significantly affected the expressions of the evaluated genes related to the innate and adaptive immune responses.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptive Immunity / immunology
  • Adult
  • Biomarkers / analysis
  • Chronic Periodontitis / complications
  • Chronic Periodontitis / immunology*
  • Cytokines / analysis*
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / immunology*
  • Female
  • Forkhead Transcription Factors / analysis
  • Gingiva / immunology
  • Humans
  • Immunity, Innate / immunology
  • Inflammation Mediators / analysis*
  • Interferon-gamma / analysis
  • Interleukin-10 / analysis
  • Interleukin-12
  • Interleukin-17 / analysis
  • Interleukin-4 / analysis
  • Interleukin-6 / analysis
  • Male
  • Middle Aged
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / analysis
  • Osteoprotegerin / analysis
  • RANK Ligand / analysis
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic / analysis
  • Toll-Like Receptor 2 / analysis
  • Toll-Like Receptor 4 / analysis
  • Transforming Growth Factor beta / analysis
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Biomarkers
  • Cytokines
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • IFNG protein, human
  • IL10 protein, human
  • IL4 protein, human
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-17
  • Interleukin-6
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • Osteoprotegerin
  • RANK Ligand
  • Receptor for Advanced Glycation End Products
  • Receptors, Immunologic
  • TLR2 protein, human
  • TLR4 protein, human
  • TNFRSF11B protein, human
  • TNFSF11 protein, human
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interleukin-12
  • Interleukin-4
  • Interferon-gamma