Omega-3 PUFA and aspirin as adjuncts to periodontal debridement in patients with periodontitis and type 2 diabetes mellitus: Randomized clinical trial

  • Nidia C. Castro dos Santos
  • , Naira M.R.B. Andere
  • , Cássia F. Araujo
  • , Andrea C. de Marco
  • , Alpdogan Kantarci
  • , Thomas E. Van Dyke
  • , Mauro P. Santamaria

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

Background: Supplementation with omega-3 polyunsaturated fatty acids (ω-3 PUFA) and low-dose aspirin (ASA) have been proposed as a host modulation regimen to control chronic inflammatory diseases. The aim of this study was to investigate the clinical and immunological impact of orally administered ω-3 PUFA and ASA as adjuncts to periodontal debridement for the treatment of periodontitis in patients type 2 diabetes. Methods: Seventy-five patients (n = 25/group) were randomly assigned to receive placebo and periodontal debridement (CG), ω-3 PUFA + ASA (3 g of fish oil/d + 100 mg ASA/d for 2 months) after periodontal debridement (test group [TG]1), or ω-3 PUFA + ASA (3 g of fish oil/d + 100 mg ASA/d for 2 months) before periodontal debridement (TG2). Periodontal parameters and GCF were collected at baseline (t0), 3 months after periodontal debridement and ω-3 PUFA + ASA or placebo for TG1 and CG (t1), after ω-3 PUFA + ASA (before periodontal debridement) for TG2 (t1), and 6 months after periodontal debridement (all groups) (t2). GCF was analyzed for cytokine levels by multiplex ELISA. Results: Ten patients (40%) in TG1 and nine patients (36%) in TG2 achieved the clinical endpoint for treatment (less than or equal to four sites with probing depth ≥ 5 mm), as opposed to four (16%) in CG. There was clinical attachment gain in moderate and deep pockets for TG1. IFN-γ and interleukin (IL)-8 levels decreased over time for both test groups. IL-6 levels were lower for TG1. HbA1c levels reduced for TG1. Conclusion: Adjunctive ω-3 and ASA after periodontal debridement provides clinical and immunological benefits to the treatment of periodontitis in patients with type 2 diabetes.

Original languageEnglish
Pages (from-to)1318-1327
Number of pages10
JournalJournal of Periodontology
Volume91
Issue number10
DOIs
StatePublished - Oct 1 2020

Bibliographical note

Publisher Copyright:
© 2020 American Academy of Periodontology

Funding

The authors would like to thank Ms. Danielle Stephens for excellent technical assistance. This study was funded by São Paulo Research Foundation (Fapesp) (Grant 2016/02234‐7 and Grant 2017/21136‐9) and the National Institute of Dental and Craniofacial Research (NIH) (USPHS Grant DE025020). The authors declare no conflict of interest.

FundersFunder number
National Institutes of Health (NIH)
National Institute of Dental and Craniofacial ResearchR01DE025020
U.S. Public Health ServiceDE025020
Fundação de Amparo à Pesquisa do Estado de São Paulo2017/21136‐9, 2016/02234‐7

    Keywords

    • aspirin
    • diabetes
    • immunomodulation
    • inflammation
    • omega-3 fatty acids
    • periodontitis

    ASJC Scopus subject areas

    • Periodontics

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