Peri-implant phenotype, calprotectin and MMP-8 levels in cases diagnosed with peri-implant disease

dc.authoridOnder, Yasemin Beliz/0000-0002-6006-3375
dc.authoridAlpaslan, Nazli Zeynep/0000-0002-6311-385X
dc.contributor.authorOnder, Yasemin Beliz
dc.contributor.authorAlpaslan, Nazli Zeynep
dc.date.accessioned2025-05-20T18:59:51Z
dc.date.issued2024
dc.departmentBilecik Şeyh Edebali Üniversitesi
dc.description.abstractObjectives The purpose of this prospective cohort study is to evaluate the effect of peri-implant phenotype (PPh) on the severity of peri-implant diseases and the results of non-surgical mechanical treatment (NSMT), along with calprotectin (CLP) and MMP-8(matrix metalloproteinase-8) levels. Materials and methods 77 implants from 39 patients were included. The implants were categorized Group-1(peri-implant mucositis), Group-2(peri-implantitis).Baseline (0. Month-PrT) clinical parameters (PD, GI, PI, BOP, CAL) and radiographic bone loss were documented, and peri-implant crevicular fluid (PICF) samples were collected. Various intruments and methodologies were employed to assess PPh components (mucosa thickness, supracrestal tissue height, keratinized mucosa) and peri-implant attached mucosa (AM). NSMT was applied to diseased implant sites. All clinical parameters were reassessed again by taking PICF samples at the 6th month-after treatment (PT). In PICF samples obtained from both groups, MMP-8 and CLP levels were evaluated using the ELISA test. Results PrT-PD,PrT-GI,PrT-CAL and PrT-BOP percentage values in Group-2 were significantly higher than Group-1.PrT-PD,PrTPI scores are significantly higher in thin biotype implants. All components of the PPh and AM were significantly lower in thin biotype. Intra-group time-dependent changes of MMP-8 and CLP were significant in both groups (p < 0.05). When the relationship between thin and thick biotype and biochemical parameters was evaluated, the change in PrT-PT didn't show a significant difference (p > 0.05). Conclusions PPh plays a role in influencing the severity of peri-implant diseases. However, the impact of phenotype on NSMT outcomes was similar in both groups.
dc.description.sponsorshipVan Yuzuncu Yil University, Van, Turkey [TDK-2021-9493]; Scientific and Technological Research Council of Turkiye (TUBIdot;TAK)
dc.description.sponsorshipThis study was funded by the authors and by Van Yuzuncu Yil University, Van, Turkey with the Project No: TDK-2021-9493.Open access funding provided by the Scientific and Technological Research Council of Turkiye (TUB & Idot;TAK)
dc.identifier.doi10.1007/s00784-024-05798-w
dc.identifier.issn1432-6981
dc.identifier.issn1436-3771
dc.identifier.issue7
dc.identifier.pmid38940878
dc.identifier.scopus2-s2.0-85197204099
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1007/s00784-024-05798-w
dc.identifier.urihttps://hdl.handle.net/11552/8666
dc.identifier.volume28
dc.identifier.wosWOS:001258672700003
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWoS
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakWoS - Science Citation Index Expanded
dc.language.isoen
dc.publisherSpringer Heidelberg
dc.relation.ispartofClinical Oral Investigations
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250518
dc.subjectCalprotectin
dc.subjectMMP-8
dc.subjectPeri-implantitis
dc.subjectPhenotype
dc.titlePeri-implant phenotype, calprotectin and MMP-8 levels in cases diagnosed with peri-implant disease
dc.typeArticle

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