Evidence map›Paper›PMID 38940878›Full record

ArticleClinical oral investigations2024

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

Yasemin Beliz Önder, Nazli Zeynep Alpaslan

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Article in Clinical oral investigations, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Yasemin Beliz ÖnderFaculty of Dentistry, Department of Periodontology, Bilecik Şeyh Edebali University, Bilecik, Turkey. ybyilmaz@gmail.com.ORCID 0000-0002-6006-3375
Nazli Zeynep AlpaslanFaculty of Dentistry, Department of Periodontology, Van Yuzuncu Yil University, Van, Turkey.ORCID 0000-0002-6311-385X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe 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

methods77 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.

resultsPrT-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).

conclusionsPPh plays a role in influencing the severity of peri-implant diseases. However, the impact of phenotype on NSMT outcomes was similar in both groups. CLINICAL RELEVANCE: The PPh should be considered when planning implant surgery.

Indexed as

Gingival Crevicular FluidLeukocyte L1 Antigen ComplexMatrix Metalloproteinase 8Peri-ImplantitisPhenotypeAdultAgedBiomarkersDental ImplantsEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedPeriodontal IndexProspective StudiesBiomarkersDental ImplantsLeukocyte L1 Antigen ComplexMatrix Metalloproteinase 8CalprotectinMMP-8Peri-implantitisPhenotype

Identifiers

PMID38940878
PMCPMC11213734

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.