Contribution of Statins towards Periodontal Treatment: A Review

Mediators Inflamm. 2019 Feb 27:2019:6367402. doi: 10.1155/2019/6367402. eCollection 2019.

Abstract

The pleiotropic effects of statins have been evaluated to assess their potential benefit in the treatment of various inflammatory and immune-mediated diseases including periodontitis. Herein, the adjunctive use of statins in periodontal therapy in vitro, in vivo, and in clinical trials was reviewed. Statins act through several pathways to modulate inflammation, immune response, bone metabolism, and bacterial clearance. They control periodontal inflammation through inhibition of proinflammatory cytokines and promotion of anti-inflammatory and/or proresolution molecule release, mainly, through the ERK, MAPK, PI3-Akt, and NF-κB pathways. Moreover, they are able to modulate the host response activated by bacterial challenge, to prevent inflammation-mediated bone resorption and to promote bone formation. Furthermore, they reduce bacterial growth, disrupt bacterial membrane stability, and increase bacterial clearance, thus averting the exacerbation of infection. Local statin delivery as adjunct to both nonsurgical and surgical periodontal therapies results in better periodontal treatment outcomes compared to systemic delivery. Moreover, combination of statin therapy with other regenerative agents improves periodontal healing response. Therefore, statins could be proposed as a potential adjuvant to periodontal therapy. However, optimization of the combination of their dose, type, and carrier could be instrumental in achieving the best treatment response.

Publication types

  • Review

MeSH terms

  • Animals
  • Cytokines / metabolism
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / metabolism
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Periodontal Diseases / drug therapy*
  • Periodontal Diseases / metabolism
  • Periodontitis / drug therapy
  • Periodontitis / metabolism

Substances

  • Cytokines
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors