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      Adjunctive Effects of a Sub-Antimicrobial Dose of Doxycycline on Clinical Parameters and Potential Biomarkers of Periodontal Tissue Catabolism

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          Abstract

          Objectives: The aim of the present randomized, double-blind, placebo-controlled, parallel-arm study was to examine the effectiveness of a sub-antimicrobial dose of doxycycline (SDD) in combination with nonsurgical periodontal therapy, compared to nonsurgical periodontal therapy alone, on potential gingival crevicular fluid (GCF) biomarkers of periodontal tissue catabolism related to the clinical outcomes over a 12-month period. Materials and Methods: GCF was collected and clinical parameters were recorded from 30 periodontitis patients randomized either to an SDD or placebo group. The SDD group received SDD (20 mg) b.i.d for 3 months plus scaling and root planing (SRP), while the placebo group was given placebo capsules b.i.d for 3 months plus SRP. The patients were evaluated every 3 months during the 12-month study period. At each visit, clinical parameters and GCF sampling were repeated. Matrix metalloproteinase (MMP)-8, MMP-9, MMP-13, myeloperoxidase (MPO), osteoprotegerin (OPG), and tartrate-resistant acid phosphatase-5 (TRAP-5) were determined by IFMA and ELISA. Results: Significant improvements were observed in all clinical parameters in both groups over 12 months ( p < 0.0125) while the SDD group showed significantly better reduction in gingival index (GI) and pocket depth and a gain in clinical attachment compared to the placebo group ( p < 0.05). GCF MMP-8 and OPG levels significantly reduced in the SDD group compared to baseline ( p < 0.05). GCF MMP-9 significantly decreased in both groups compared to baseline ( p < 0.05). GCF MPO significantly decreased at 3 and 9 months in the SDD group, while it significantly decreased at 6 months in the placebo group ( p < 0.05). TRAP and MMP-13 could be detected in none of the samples. Conclusions: The present results indicate that three months of adjunctive usage of SDD to nonsurgical periodontal therapy compared to nonsurgical periodontal therapy alone in periodontitis patients results in further improvement of clinical periodontal parameters and GCF markers of periodontal tissue breakdown over a 12-month period. Beneficial effects of adjunctive SDD therapy is likely to be related to the reduced levels of two major periodontitis-associated MMPs, MMP-8 and -9, and their potential oxidative activator MPO.

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          Most cited references64

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          Mechanisms of Bone Resorption in Periodontitis

          Alveolar bone loss is a hallmark of periodontitis progression and its prevention is a key clinical challenge in periodontal disease treatment. Bone destruction is mediated by the host immune and inflammatory response to the microbial challenge. However, the mechanisms by which the local immune response against periodontopathic bacteria disturbs the homeostatic balance of bone formation and resorption in favour of bone loss remain to be established. The osteoclast, the principal bone resorptive cell, differentiates from monocyte/macrophage precursors under the regulation of the critical cytokines macrophage colony-stimulating factor, RANK ligand, and osteoprotegerin. TNF-α, IL-1, and PGE2 also promote osteoclast activity, particularly in states of inflammatory osteolysis such as those found in periodontitis. The pathogenic processes of destructive inflammatory periodontal diseases are instigated by subgingival plaque microflora and factors such as lipopolysaccharides derived from specific pathogens. These are propagated by host inflammatory and immune cell influences, and the activation of T and B cells initiates the adaptive immune response via regulation of the Th1-Th2-Th17 regulatory axis. In summary, Th1-type T lymphocytes, B cell macrophages, and neutrophils promote bone loss through upregulated production of proinflammatory mediators and activation of the RANK-L expression pathways.
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            Reduced plaque formation by the chloromethyl analogue of victamine C.

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              Matrix metalloproteinases: contribution to pathogenesis, diagnosis and treatment of periodontal inflammation.

              Matrix metalloproteinases (MMPs) form a family of enzymes that mediate multiple functions both in the tissue destruction and immune responses related to periodontal inflammation. The expression and activity of MMPs in non-inflamed periodontium is low but is drastically enhanced to pathologically elevated levels due to the dental plaque and infection-induced periodontal inflammation. Soft and hard tissue destruction during periodontitis and peri-implantitis are thought to reflect a cascade of events involving bacterial virulence factors/enzymes, pro-inflammatory cytokines, reactive oxygen species and MMPs. However, recent studies suggest that MMPs can also exert anti-inflammatory effects in defence of the host by processing anti-inflammatory cytokines and chemokines, as well as by regulating apoptotic and immune responses. MMP-inhibitor (MMPI)-drugs, such as doxycycline, can be used as adjunctive medication to augment both the scaling and root planing-treatment of periodontitis locally and to reduce inflammation systematically. Furthermore, MMPs present in oral fluids (gingival crevicular fluid (GCF), peri-implant sulcular fluid (PISF), mouth-rinses and saliva) can be utilized to develop new non-invasive, chair/bed-side, point-of-care diagnostics for periodontitis and dental peri-implantitis.
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                Author and article information

                Journal
                Dent J (Basel)
                Dent J (Basel)
                dentistry
                Dentistry Journal
                MDPI
                2304-6767
                20 January 2019
                March 2019
                : 7
                : 1
                : 9
                Affiliations
                [1 ]School of Dentistry, Department of Periodontology, Ege University, İzmir 35100, Turkey; aligurkan00@ 123456yahoo.com
                [2 ]Department of Oral and Maxillofacial Diseases, University of Helsinki, Helsinki University Hospital, 00014 Helsinki, Finland; taina.tervahartiala@ 123456helsinki.fi (T.T.); timo.sorsa@ 123456helsinki.fi (T.S.); saeed.alassiri@ 123456helsinki.fi (S.A.)
                [3 ]Laboratory of Periodontal Biology and Dentistry, University of Chile, Santiago 8380492, Chile; mhernandezrios@ 123456gmail.com
                [4 ]Dentistry Unit, Faculty of Health Sciences, Universidad Autόnomia de Chile, Santiago 8910132, Chile
                [5 ]School of Medicine, Department of Medical Informatics, Ege University, İzmir 35100, Turkey; semihaozgul@ 123456hotmail.com
                [6 ]Department of Dental Medicine, Division of Periodontology, Karolinska Institutet, Stockholm 14104, Sweden
                Author notes
                [* ]Correspondence: gemingil@ 123456yahoo.com
                Author information
                https://orcid.org/0000-0002-4869-9629
                https://orcid.org/0000-0001-8289-7314
                Article
                dentistry-07-00009
                10.3390/dj7010009
                6473443
                30669541
                8bbfb598-ae7d-4e48-9d9d-30728b201cd9
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 11 November 2018
                : 08 January 2019
                Categories
                Article

                subantimicrobial-dose doxycycline,scaling and root planning,gingival crevicular fluid,adjunctive therapy

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