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Omega-3 and aspirin in the nonsurgical treatment of grade C periodontitis: A randomized clinical trial

dc.contributor.authorAraujo, Cássia F. [UNESP]
dc.contributor.authorAndere, Naira M. R. B. [UNESP]
dc.contributor.authorCastro dos Santos, Nidia C.
dc.contributor.authorFerraz, Laís F. F. [UNESP]
dc.contributor.authorMiguel, Manuela M. V. [UNESP]
dc.contributor.authorMathias-Santamaria, Ingrid F.
dc.contributor.authorMonteiro, Mabelle F.
dc.contributor.authorShaddox, Luciana M.
dc.contributor.authorCasarin, Renato C. V.
dc.contributor.authorSantamaria, Mauro P. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFaculdade Santo Antônio
dc.contributor.institutionGuarulhos University
dc.contributor.institutionUniversity of Kentucky
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2025-04-29T20:11:00Z
dc.date.issued2025-01-01
dc.description.abstractBackground: The use of omega-3 (Ω-3) polyunsaturated fatty acids and acetylsalicylic acid (ASA, aspirin) has shown better clinical outcomes in the treatment of periodontitis compared to nonsurgical periodontal therapy (NSPT) alone. This randomized clinical trial aimed to evaluate the use of 900 mg Ω-3 and 100 mg ASA for 180 days as adjuncts to NSPT for generalized stage III–IV grade C periodontitis (GCP). Methods: Patients underwent subgingival debridement (SD) associated with Ω-3+ASA or cellulose placebo and received monthly prophylaxis. Clinical and immunological parameters were compared at baseline, 3, and 6 months after treatment. The daily dose of Ω-3 consisted of 540 mg eicosapentaenoic acid (EPA) and 360 mg docosahexaenoic acid (DHA). Results: Thirty-eight patients, 12 males (7 in the SD+Ω-3+AAS group and 5 in the SD+Placebo group; p > 0.05), with a mean age of 32.84 ± 5.47 and 30.42 ± 5.79 years, respectively (p > 0.05), were included. Both groups showed significant improvements (p < 0.05) in all full-mouth parameters. Reductions in the number of pockets, mean probing depth (PD), and clinical attachment level of moderate and deep sites, as well as the number and percentage of residual pockets, were observed (intragroup p < 0.05; intergroup p > 0.05). However, residual pockets' mean PD decrease (p < 0.05) was only observed at 6 months in the SD+Ω-3+ASA group. The concentration of interleukin (IL)-1β from moderate and deep pockets decreased (p < 0.05) in both groups. The matrix metalloproteinase (MMP)-9 to tissue metalloproteinase inhibitor (TIMP)-1 ratio in the SD+Placebo group at 3 months revealed a proinflammatory profile in moderate (intergroup p = 0.006) and deep pockets (intergroup p < 0.001). Conclusion: Ω-3+ASA therapy did not add clinical benefits to the NSPT for generalized stage III–IV GCP, although some immunomodulatory benefits could be observed. Plain language summary: The use of omega-3 (Ω-3) and aspirin (ASA) along with subgingival debridement (SD) for root decontamination of periodontal pockets has shown better results in the nonsurgical treatment of gum disease and bone loss compared to SD alone. This investigation aimed to evaluate the use of 900 mg Ω-3 and 100 mg ASA for 180 days as adjuncts to the treatment of patients with gum disease and rapid bone loss rate. Thirty-eight patients underwent SD associated with Ω-3+ASA or placebo. Clinical and immunological parameters were evaluated at the beginning of the study and 3 and 6 months after. Both groups showed significant improvements. A significant reduction in the number of sites with diseased pockets was observed. The number of residual diseased sites was also significantly reduced, without differences between the groups. However, a significant decrease in the pocket size of the diseased sites was only observed at 6 months in the group that received Ω-3+ASA. The concentration of interleukin (IL)-1β (a protein present in the inflammatory process) from diseased sites significantly decreased in both groups. We concluded that the proposed therapy did not add any significant clinical benefits for patients with gum disease and rapid bone loss rate.en
dc.description.affiliationDepartment of Diagnosis and Surgery Division of Periodontology Institute of Science and Technology São Paulo State University, São Paulo
dc.description.affiliationDivision of Dentistry Faculdade Santo Antônio, São Paulo
dc.description.affiliationDental Research Division Guarulhos University, São Paulo
dc.description.affiliationDepartment of Oral Health Practice College of Dentistry University of Kentucky
dc.description.affiliationDepartment of Periodontics and Prosthodontics Division of Periodontics Piracicaba Dental School University of Campinas, São Paulo
dc.description.affiliationUnespDepartment of Diagnosis and Surgery Division of Periodontology Institute of Science and Technology São Paulo State University, São Paulo
dc.identifierhttp://dx.doi.org/10.1002/JPER.24-0322
dc.identifier.citationJournal of Periodontology.
dc.identifier.doi10.1002/JPER.24-0322
dc.identifier.issn0022-3492
dc.identifier.scopus2-s2.0-85219672515
dc.identifier.urihttps://hdl.handle.net/11449/308007
dc.language.isoeng
dc.relation.ispartofJournal of Periodontology
dc.sourceScopus
dc.subjectaspirin
dc.subjectimmunomodulation
dc.subjectinflammation
dc.subjectomega-3 fatty acids
dc.subjectperiodontal debridement
dc.subjectperiodontitis
dc.titleOmega-3 and aspirin in the nonsurgical treatment of grade C periodontitis: A randomized clinical trialen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0002-8918-5472[1]
unesp.author.orcid0000-0003-4832-2407[2]
unesp.author.orcid0000-0003-2041-9426[3]
unesp.author.orcid0000-0003-4486-6335[4]
unesp.author.orcid0000-0003-4828-3487[5]
unesp.author.orcid0000-0003-2518-0135[6]
unesp.author.orcid0000-0001-9333-4349[7]
unesp.author.orcid0000-0003-0948-1667[8]
unesp.author.orcid0000-0003-1743-5855[9]
unesp.author.orcid0000-0001-9468-0729[10]

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