TY - JOUR
T1 - Evaluation of DNA methylation of inflammatory genes following treatment of chronic periodontitis
T2 - A pilot case–control study
AU - Asa'ad, Farah
AU - Bollati, Valentina
AU - Pagni, Giorgio
AU - Castilho, Rogerio M.
AU - Rossi, Eleonora
AU - Pomingi, Francesca
AU - Tarantini, Letizia
AU - Consonni, Dario
AU - Giannobile, William V.
AU - Rasperini, Giulio
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Objective: To evaluate the influence of periodontal therapy on DNA methylation in patients with chronic periodontitis as compared to healthy individuals. Material and Methods: Twenty patients were enrolled into two groups: (i) 10 diagnosed as clinically healthy; and (ii) 10 diagnosed with chronic periodontitis. Clinical measures were recorded and gingival biopsies were harvested at baseline (both patient groups) and at 2 and 8 weeks post-baseline for diseased individuals. Molecular DNA methylation analysis was performed by pyrosequencing for the putative inflammation-associated genes LINE-1, COX-2, IFN-γ and TNF-α. Random-intercept linear regression models were applied to evaluate methylation levels across groups at baseline and the methylation changes over time in the diseased and normal tissues. Results: Periodontal therapy did not influence gene expression methylation of TNF-α, IFN-γ and LINE-1 levels at normal and periodontitis sites over time. However, it significantly reduced COX-2 methylation levels comparable to healthy individuals at both 2 and 8 weeks post-treatment (p <.05). Conclusions: Periodontal therapy resets the DNA methylation status of inflammatory gene for COX-2 in patients with periodontal disease. DNA methylation levels of TNF-α, IFN-γ and LINE-1 were sustained in periodontitis sites despite therapy. Future studies should consider an expanded panel of inflammatory genes over time. (ClinicalTrials.gov NCT02835898).
AB - Objective: To evaluate the influence of periodontal therapy on DNA methylation in patients with chronic periodontitis as compared to healthy individuals. Material and Methods: Twenty patients were enrolled into two groups: (i) 10 diagnosed as clinically healthy; and (ii) 10 diagnosed with chronic periodontitis. Clinical measures were recorded and gingival biopsies were harvested at baseline (both patient groups) and at 2 and 8 weeks post-baseline for diseased individuals. Molecular DNA methylation analysis was performed by pyrosequencing for the putative inflammation-associated genes LINE-1, COX-2, IFN-γ and TNF-α. Random-intercept linear regression models were applied to evaluate methylation levels across groups at baseline and the methylation changes over time in the diseased and normal tissues. Results: Periodontal therapy did not influence gene expression methylation of TNF-α, IFN-γ and LINE-1 levels at normal and periodontitis sites over time. However, it significantly reduced COX-2 methylation levels comparable to healthy individuals at both 2 and 8 weeks post-treatment (p <.05). Conclusions: Periodontal therapy resets the DNA methylation status of inflammatory gene for COX-2 in patients with periodontal disease. DNA methylation levels of TNF-α, IFN-γ and LINE-1 were sustained in periodontitis sites despite therapy. Future studies should consider an expanded panel of inflammatory genes over time. (ClinicalTrials.gov NCT02835898).
KW - biomarkers
KW - DNA methylation
KW - epigenetics
KW - inflammatory genes
KW - periodontal disease pathogenesis
KW - periodontal diseases/therapy
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U2 - 10.1111/jcpe.12783
DO - 10.1111/jcpe.12783
M3 - Article
AN - SCOPUS:85027511239
SN - 0303-6979
VL - 44
SP - 905
EP - 914
JO - Journal of Clinical Periodontology
JF - Journal of Clinical Periodontology
IS - 9
ER -