Publication:
Comparison of Keratinocyte Proliferation in Diabetic and Non-Diabetic Inflamed Gingiva

dc.authorscopusid6603291949
dc.authorscopusid24477464400
dc.authorscopusid6701347162
dc.contributor.authorAçikgöz, G.
dc.contributor.authorDevrim, I.
dc.contributor.authorÖzdamar, Ş.
dc.date.accessioned2020-06-21T15:38:48Z
dc.date.available2020-06-21T15:38:48Z
dc.date.issued2004
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Açikgöz] Gökhan, Department of Periodontology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Devrim] Inci, Department of Periodontology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Özdamar] Şükrü Oĝuz, Department of Pathology, Hacettepe Üniversitesi, Ankara, Turkeyen_US
dc.description.abstractBackground: Keratinocytes are chiefly cells of the epidermis but also constitute 90% of the gingival cells. The molecular mechanisms of proliferative activity in keratinization whereby diabetes alters periodontal physiology have not been elucidated. In this study, we aimed to investigate the role of gingival keratinocytes in hyperglycemic subjects by examining their mitotic activities. Methods: We tested 30 patients with periodontitis, of whom 15 were type II diabetics and the remainder systemically healthy. Biopsies were obtained from the bottom of the deepest pocket in each subject by reverse beveled incision. Formalin-fixed and paraffin-embedded specimens were then processed for periodic acid-Schiff (PAS)-diastase histochemistry and proliferating cell nuclear antigen (PCNA) (P10). Immunohistochemical studies were employed to determine the presence of PCNA and were used to detect the proliferating potential of keratinocytes needed in synthesizing DNA. The expression of PCNA was evaluated using an immunoperoxidase technique and PC10 monoclonal antibody to PCNA. Mitotic index was calculated from basal cells. Statistical analysis employed the chi-square test. Results: No significant difference between the diabetic and non-diabetic patients was found in the mitotic index of the oral-gingival epithelium. Conclusion: Although the mitotic index in patients with diabetes was slightly lower, keratinization in the gingival tissues for both groups was essentially identical.en_US
dc.identifier.doi10.1902/jop.2004.75.7.989
dc.identifier.endpage994en_US
dc.identifier.issn0022-3492
dc.identifier.issn1943-3670
dc.identifier.issue7en_US
dc.identifier.pmid15341357
dc.identifier.scopus2-s2.0-4444234240
dc.identifier.scopusqualityQ1
dc.identifier.startpage989en_US
dc.identifier.urihttps://doi.org/10.1902/jop.2004.75.7.989
dc.identifier.volume75en_US
dc.identifier.wosWOS:000222956900010
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherAmer. Acad. Periodontologyen_US
dc.relation.ispartofJournal of Periodontologyen_US
dc.relation.journalJournal of Periodontologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectGingiva/Anatomy and Physiologyen_US
dc.subjectKeratinocytesen_US
dc.subjectMitosisen_US
dc.subjectPeriodontal Diseases/Metabolismen_US
dc.titleComparison of Keratinocyte Proliferation in Diabetic and Non-Diabetic Inflamed Gingivaen_US
dc.typeArticleen_US
dspace.entity.typePublication

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