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Histological characteristics of advanced peri-implantitis bone defects in humans
BACKGROUND: Inflammatory osteolysis is the clinical hallmark of peri-implantitis. The morphology of the remaining peri-implant bone and the level of osseointegration, however, remain unknown. Our aim was to characterize advanced peri-implantitis bone defects in humans. METHODS: Four patients (3 fema...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093613/ https://www.ncbi.nlm.nih.gov/pubmed/32211972 http://dx.doi.org/10.1186/s40729-020-00208-8 |
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author | Galárraga-Vinueza, Maria Elisa Tangl, Stefan Bianchini, Marco Magini, Ricardo Obreja, Karina Gruber, Reinhard Schwarz, Frank |
author_facet | Galárraga-Vinueza, Maria Elisa Tangl, Stefan Bianchini, Marco Magini, Ricardo Obreja, Karina Gruber, Reinhard Schwarz, Frank |
author_sort | Galárraga-Vinueza, Maria Elisa |
collection | PubMed |
description | BACKGROUND: Inflammatory osteolysis is the clinical hallmark of peri-implantitis. The morphology of the remaining peri-implant bone and the level of osseointegration, however, remain unknown. Our aim was to characterize advanced peri-implantitis bone defects in humans. METHODS: Four patients (3 female and 1 male) were diagnosed with peri-implantitis. A total of 5 implants with machined surfaces and a mean loading time of 12 ± 6 years were removed due to advanced bone loss. The defect extension, the peri-implant bone density (bone area per tissue area in percentage), bone-to-implant contact (%), and the number of filled and empty osteocyte lacunae were calculated based on undecalcified histological specimens. RESULTS: The defect extension was on average 4.2 mm (95% CI 0.8–3.4). Remaining peri-implant bone showed a high density of 85.5% (95% CI 79.1–91.3) and covered in total 74% (95% CI 70.5–77.5) of the implant surface. Filled and empty osteocyte lacunae density was on average 191 and 165/mm(2) (95% CI 132–251; 103–225), respectively. Histology further revealed signs of ongoing bone formation and resorption. CONCLUSION: There are signs that suggest that once the original cortical bone is lost due to peri-implantitis, the remaining apical trabecular bone is reinforced and transformed into cortical bone that might take over the functional load. |
format | Online Article Text |
id | pubmed-7093613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70936132020-03-27 Histological characteristics of advanced peri-implantitis bone defects in humans Galárraga-Vinueza, Maria Elisa Tangl, Stefan Bianchini, Marco Magini, Ricardo Obreja, Karina Gruber, Reinhard Schwarz, Frank Int J Implant Dent Research BACKGROUND: Inflammatory osteolysis is the clinical hallmark of peri-implantitis. The morphology of the remaining peri-implant bone and the level of osseointegration, however, remain unknown. Our aim was to characterize advanced peri-implantitis bone defects in humans. METHODS: Four patients (3 female and 1 male) were diagnosed with peri-implantitis. A total of 5 implants with machined surfaces and a mean loading time of 12 ± 6 years were removed due to advanced bone loss. The defect extension, the peri-implant bone density (bone area per tissue area in percentage), bone-to-implant contact (%), and the number of filled and empty osteocyte lacunae were calculated based on undecalcified histological specimens. RESULTS: The defect extension was on average 4.2 mm (95% CI 0.8–3.4). Remaining peri-implant bone showed a high density of 85.5% (95% CI 79.1–91.3) and covered in total 74% (95% CI 70.5–77.5) of the implant surface. Filled and empty osteocyte lacunae density was on average 191 and 165/mm(2) (95% CI 132–251; 103–225), respectively. Histology further revealed signs of ongoing bone formation and resorption. CONCLUSION: There are signs that suggest that once the original cortical bone is lost due to peri-implantitis, the remaining apical trabecular bone is reinforced and transformed into cortical bone that might take over the functional load. Springer Berlin Heidelberg 2020-03-25 /pmc/articles/PMC7093613/ /pubmed/32211972 http://dx.doi.org/10.1186/s40729-020-00208-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Galárraga-Vinueza, Maria Elisa Tangl, Stefan Bianchini, Marco Magini, Ricardo Obreja, Karina Gruber, Reinhard Schwarz, Frank Histological characteristics of advanced peri-implantitis bone defects in humans |
title | Histological characteristics of advanced peri-implantitis bone defects in humans |
title_full | Histological characteristics of advanced peri-implantitis bone defects in humans |
title_fullStr | Histological characteristics of advanced peri-implantitis bone defects in humans |
title_full_unstemmed | Histological characteristics of advanced peri-implantitis bone defects in humans |
title_short | Histological characteristics of advanced peri-implantitis bone defects in humans |
title_sort | histological characteristics of advanced peri-implantitis bone defects in humans |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093613/ https://www.ncbi.nlm.nih.gov/pubmed/32211972 http://dx.doi.org/10.1186/s40729-020-00208-8 |
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