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Characterization of the apical bridge barrier formed following amelogenin apexification
BACKGROUND: Recombinant amelogenin protein (RAP) is reported to induce complete root apex formation in dog model when used as apexification therapy. It also induces pulp regeneration in 85% of the treated group. Thus, the aim of this study was to investigate the nature of the remaining regenerated c...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280449/ https://www.ncbi.nlm.nih.gov/pubmed/30514371 http://dx.doi.org/10.1186/s12903-018-0641-0 |
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author | Mounir, Maha M. F. Farsi, Jamila M. A. Alhazzazi, Turki Y. Matar, Moustafa A. El-Housseiny, Azza A. |
author_facet | Mounir, Maha M. F. Farsi, Jamila M. A. Alhazzazi, Turki Y. Matar, Moustafa A. El-Housseiny, Azza A. |
author_sort | Mounir, Maha M. F. |
collection | PubMed |
description | BACKGROUND: Recombinant amelogenin protein (RAP) is reported to induce complete root apex formation in dog model when used as apexification therapy. It also induces pulp regeneration in 85% of the treated group. Thus, the aim of this study was to investigate the nature of the remaining regenerated calcified tissues of the RAP group that showed no pulp regeneration compared to the calcium hydroxide treated group (CH). METHODS: A total of 240 dogs’ open apex root canals were used, after establishment of canals contamination. Canals were cleaned, irrigated, and filled with RAP as an apexification material and compared with CH. Treated teeth were assessed by H&E, trichrome staining, and/or immunohistochemistry technique, at 1, 3, and 6 months. RESULTS: A time-dependent increase in the calcified tissue barrier was observed in the apex of the RAP-treated group compared to the CH-treated group. The newly formed dentin in this RAP group was mainly tubular dentin and was functionally attached to the bone by periodontal ligament, while the CH group showed dentin-associated mineralized tissue (DAMT) associated with the newly formed apical barrier. CONCLUSIONS: Out results suggest that RAP can be used as novel apexification material, resulting in a thickening and strengthening of the canal walls, and achieving apical closure. |
format | Online Article Text |
id | pubmed-6280449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62804492018-12-10 Characterization of the apical bridge barrier formed following amelogenin apexification Mounir, Maha M. F. Farsi, Jamila M. A. Alhazzazi, Turki Y. Matar, Moustafa A. El-Housseiny, Azza A. BMC Oral Health Research Article BACKGROUND: Recombinant amelogenin protein (RAP) is reported to induce complete root apex formation in dog model when used as apexification therapy. It also induces pulp regeneration in 85% of the treated group. Thus, the aim of this study was to investigate the nature of the remaining regenerated calcified tissues of the RAP group that showed no pulp regeneration compared to the calcium hydroxide treated group (CH). METHODS: A total of 240 dogs’ open apex root canals were used, after establishment of canals contamination. Canals were cleaned, irrigated, and filled with RAP as an apexification material and compared with CH. Treated teeth were assessed by H&E, trichrome staining, and/or immunohistochemistry technique, at 1, 3, and 6 months. RESULTS: A time-dependent increase in the calcified tissue barrier was observed in the apex of the RAP-treated group compared to the CH-treated group. The newly formed dentin in this RAP group was mainly tubular dentin and was functionally attached to the bone by periodontal ligament, while the CH group showed dentin-associated mineralized tissue (DAMT) associated with the newly formed apical barrier. CONCLUSIONS: Out results suggest that RAP can be used as novel apexification material, resulting in a thickening and strengthening of the canal walls, and achieving apical closure. BioMed Central 2018-12-04 /pmc/articles/PMC6280449/ /pubmed/30514371 http://dx.doi.org/10.1186/s12903-018-0641-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Mounir, Maha M. F. Farsi, Jamila M. A. Alhazzazi, Turki Y. Matar, Moustafa A. El-Housseiny, Azza A. Characterization of the apical bridge barrier formed following amelogenin apexification |
title | Characterization of the apical bridge barrier formed following amelogenin apexification |
title_full | Characterization of the apical bridge barrier formed following amelogenin apexification |
title_fullStr | Characterization of the apical bridge barrier formed following amelogenin apexification |
title_full_unstemmed | Characterization of the apical bridge barrier formed following amelogenin apexification |
title_short | Characterization of the apical bridge barrier formed following amelogenin apexification |
title_sort | characterization of the apical bridge barrier formed following amelogenin apexification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6280449/ https://www.ncbi.nlm.nih.gov/pubmed/30514371 http://dx.doi.org/10.1186/s12903-018-0641-0 |
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