Publication:
Neurogenic Inflammation in Periimplant and Periodontal Disease: A Case–Control Split-Mouth Study

dc.authorscopusid54390095500
dc.authorscopusid6602760999
dc.authorscopusid16031909300
dc.authorscopusid57002980900
dc.authorscopusid57209338190
dc.authorscopusid16746539800
dc.contributor.authorSert, S.
dc.contributor.authorSakallioǧlu, U.
dc.contributor.authorLütfiog̊lu, M.
dc.contributor.authorAydoğdu, A.
dc.contributor.authorAcarel, E.
dc.contributor.authorGünaydin, M.
dc.date.accessioned2020-06-21T12:26:14Z
dc.date.available2020-06-21T12:26:14Z
dc.date.issued2019
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Sert] Sertaç, Department of Periodontology, Ankara Center of Oral and Dental Health, Ankara, Turkiye, Turkey; [Sakallioǧlu] Umur, Department of Periodontology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Lütfiog̊lu] Müge, Department of Periodontology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aydoğdu] Ahmet, Department of Periodontology, Bezmi Alem University, Istanbul, Istanbul, Turkey; [Acarel] Elif Eser, Department of Periodontology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Günaydin] Murat, Department of Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractObjective: Although the regulatory effects of substance-P (SP), neurokinin-A (NKA), calcitonin gene-linked peptide (CGRP) and neuropeptide-Y (NPY) on periodontal inflammatory responses have been described, the effects of these neuropeptides on healthy and diseased periimplant tissues are not clearly defined. Materials and methods: Thirty-nine implants loaded at least for 12 months with their symmetrically matching teeth were evaluated and compared by a split-mouth study design. Six study groups were created in this regard as follows: group 1 (healthy periodontal tissues), group 2 (healthy periimplant tissues), group 3 (gingivitis), group 4 (periimplant mucositis), group 5 (periodontitis) and group 6 (periimplantitis). Clinical examinations included Silness–Löe plaque index, Löe–Silness gingival index, bleeding on probing, probing pocket depth and clinical attachment level measurements. Gingival crevicular fluid and periimplant sulcular fluid samples were collected, and the concentrations of neuropeptides were determined by enzyme-linked immunosorbent assay. Their levels and correlations were investigated together with the clinical parameters. Results: Neuropeptide levels were different in the teeth and implant groups according to the periodontal status (p < 0.001). SP and NKA levels were increased, whereas CGRP and NPY levels were decreased in the diseased states. There were no differences between the neuropeptide levels of matching teeth and implants (groups 1–2, groups 3–4 and groups 5–6; p > 0.05). Conclusion: Our study demonstrated the presence of local neuropeptides in healthy and diseased periimplant tissues. The neurogenic inflammatory responses were also found to be similar in both periimplant and periodontal tissues. © 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltden_US
dc.identifier.doi10.1111/clr.13486
dc.identifier.endpage807en_US
dc.identifier.issn0905-7161
dc.identifier.issn1600-0501
dc.identifier.issue8en_US
dc.identifier.pmid31121061
dc.identifier.scopus2-s2.0-85067518975
dc.identifier.scopusqualityQ1
dc.identifier.startpage800en_US
dc.identifier.urihttps://doi.org/10.1111/clr.13486
dc.identifier.volume30en_US
dc.identifier.wosWOS:000479265600009
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherBlackwell Munksgaard info@mks.blackwellpublising.comen_US
dc.relation.ispartofClinical Oral Implants Researchen_US
dc.relation.journalClinical Oral Implants Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGingivitisen_US
dc.subjectInflammationen_US
dc.subjectNeuropeptidesen_US
dc.subjectPeriimplantitisen_US
dc.subjectPeriodontitisen_US
dc.titleNeurogenic Inflammation in Periimplant and Periodontal Disease: A Case–Control Split-Mouth Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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