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Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses

OBJECTIVES: To compare in persons aged 70 years or older the clinical and inflammatory changes occurring around implants and natural teeth during and after a phase of undisturbed plaque accumulation. MATERIAL AND METHODS: Twenty partially edentulous participants with titanium implants refrained from...

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Autores principales: Meyer, Simon, Giannopoulou, Catherine, Courvoisier, Delphine, Schimmel, Martin, Müller, Frauke, Mombelli, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599942/
https://www.ncbi.nlm.nih.gov/pubmed/27333829
http://dx.doi.org/10.1111/clr.12912
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author Meyer, Simon
Giannopoulou, Catherine
Courvoisier, Delphine
Schimmel, Martin
Müller, Frauke
Mombelli, Andrea
author_facet Meyer, Simon
Giannopoulou, Catherine
Courvoisier, Delphine
Schimmel, Martin
Müller, Frauke
Mombelli, Andrea
author_sort Meyer, Simon
collection PubMed
description OBJECTIVES: To compare in persons aged 70 years or older the clinical and inflammatory changes occurring around implants and natural teeth during and after a phase of undisturbed plaque accumulation. MATERIAL AND METHODS: Twenty partially edentulous participants with titanium implants refrained from oral hygiene practices while being clinically monitored in weekly intervals for 21 days. Teeth and implants were then cleaned, oral hygiene resumed, and the participants were further monitored for 3 weeks. Twelve biomarkers were assessed in gingival and peri‐implant crevicular fluid (GCF, PCF). RESULTS: During 3 weeks of oral hygiene abstention, the gingival index (GI) continuously increased. On day 21, there were significantly more sites with GI >1 at implants than at teeth. After restarting oral hygiene, the GI decreased markedly in both groups. Throughout the experiment, the plaque index was significantly higher on teeth than on implants. The different biomarkers reacted variably. IL‐1β increased significantly with plaque accumulation. IL‐1β, GM‐CSF, TNF‐α, and IFN‐γ were significantly higher in GCF compared to PCF at day 21. IL‐8 decreased significantly in GCF up to day 14. MIP‐1β decreased significantly in GCF, but not in PCF. At the 3‐week follow‐up, the levels of all biomarkers assessed in GCF and PCF had returned to baseline values. CONCLUSIONS: In an elderly cohort, plaque accumulation induced an inflammatory reaction around both teeth and implants. Although there was less plaque accumulation on implants, the peri‐implant mucosa showed a stronger clinical response than gingiva.
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spelling pubmed-55999422017-10-02 Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses Meyer, Simon Giannopoulou, Catherine Courvoisier, Delphine Schimmel, Martin Müller, Frauke Mombelli, Andrea Clin Oral Implants Res Original Articles OBJECTIVES: To compare in persons aged 70 years or older the clinical and inflammatory changes occurring around implants and natural teeth during and after a phase of undisturbed plaque accumulation. MATERIAL AND METHODS: Twenty partially edentulous participants with titanium implants refrained from oral hygiene practices while being clinically monitored in weekly intervals for 21 days. Teeth and implants were then cleaned, oral hygiene resumed, and the participants were further monitored for 3 weeks. Twelve biomarkers were assessed in gingival and peri‐implant crevicular fluid (GCF, PCF). RESULTS: During 3 weeks of oral hygiene abstention, the gingival index (GI) continuously increased. On day 21, there were significantly more sites with GI >1 at implants than at teeth. After restarting oral hygiene, the GI decreased markedly in both groups. Throughout the experiment, the plaque index was significantly higher on teeth than on implants. The different biomarkers reacted variably. IL‐1β increased significantly with plaque accumulation. IL‐1β, GM‐CSF, TNF‐α, and IFN‐γ were significantly higher in GCF compared to PCF at day 21. IL‐8 decreased significantly in GCF up to day 14. MIP‐1β decreased significantly in GCF, but not in PCF. At the 3‐week follow‐up, the levels of all biomarkers assessed in GCF and PCF had returned to baseline values. CONCLUSIONS: In an elderly cohort, plaque accumulation induced an inflammatory reaction around both teeth and implants. Although there was less plaque accumulation on implants, the peri‐implant mucosa showed a stronger clinical response than gingiva. John Wiley and Sons Inc. 2016-06-23 2017-08 /pmc/articles/PMC5599942/ /pubmed/27333829 http://dx.doi.org/10.1111/clr.12912 Text en © 2016 The Authors. Clinical Oral Implants Research Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Meyer, Simon
Giannopoulou, Catherine
Courvoisier, Delphine
Schimmel, Martin
Müller, Frauke
Mombelli, Andrea
Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title_full Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title_fullStr Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title_full_unstemmed Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title_short Experimental mucositis and experimental gingivitis in persons aged 70 or over. Clinical and biological responses
title_sort experimental mucositis and experimental gingivitis in persons aged 70 or over. clinical and biological responses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599942/
https://www.ncbi.nlm.nih.gov/pubmed/27333829
http://dx.doi.org/10.1111/clr.12912
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