The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model

Detalhes bibliográficos
Autor(a) principal: Silva, Jonathan Ribeiro da
Data de Publicação: 2021
Outros Autores: Balbas, Maria Cristina de Moraes, Correa, Caroline Agueda, Zanela, Manuella, Okamoto, Roberta [UNESP], Pereira, Rodrigo dos Santos, Homsi, Nicolas, Hochuli-Vieira, Eduardo [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1177/19433875211048367
http://hdl.handle.net/11449/218701
Resumo: Objective: To evaluate the effects of inorganic bovine bone graft (Lumina Bone, Criteria, Brazil) and beta-tricalcium phosphate (beta-TCP) graft (ChronOS, Synthes, Brazil) in rats with the risk of developing post-extraction medication-related osteonecrosis of the jaw (MRONJ). Methods: Eighteen male Wistar rats weighing 350 to 450 g were induced to develop MRONJ using zoledronic acid for 5 weeks. In the sixth week, the right maxillary first molar was extracted. The animals in Group I (G1) did not receive bone grafts after tooth extraction, while Group II (G2) animals received inorganic bovine bone grafts, and Group III (G3) animals received beta-tricalcium phosphate (beta-TCP) grafts. Clinical evaluation and histomorphometric and immunohistochemical analyses were performed. ANOVA and Tukey's statistical tests were used and a level of significance was considered to be 5%. Results: In the clinical evaluation, animals from G2 and G3 did not present clinical manifestations of osteonecrosis, unlike the control group (G1) animals, which presented necrotic bone tissue exposure in all samples. In the histomorphometric evaluation, animals in G3 showed greater formation of bone tissue (66%) and less formation of bone lacuna (18%) than animals in G1 (58%/32%) and in G2 (59%/27%) (P < 0.05). Moderate (++) immunostaining was observed in G2 and G3 for RANKL, TRAP, and OC, while G1 showed moderate (++) labeling for OC and mild (+) immunostaining for TRAP and RANKL. Conclusions: Greater formation of bone tissue and fewer bone lacunae were found in animals treated with beta-TCP. In clinical evaluation, bone graft groups presented with the clinical manifestation of MRONJ and showed higher intensity of immunostaining for TRAP and RANKL. Despite the limitations of experimental animal studies, the results of this work may assist in the development of future clinical research for the prevention of MRONJ.
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spelling The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Modelbisphosphonateosteonecrosisbone graftbisphosphonate-associated osteonecrosis of the jawratsWistarObjective: To evaluate the effects of inorganic bovine bone graft (Lumina Bone, Criteria, Brazil) and beta-tricalcium phosphate (beta-TCP) graft (ChronOS, Synthes, Brazil) in rats with the risk of developing post-extraction medication-related osteonecrosis of the jaw (MRONJ). Methods: Eighteen male Wistar rats weighing 350 to 450 g were induced to develop MRONJ using zoledronic acid for 5 weeks. In the sixth week, the right maxillary first molar was extracted. The animals in Group I (G1) did not receive bone grafts after tooth extraction, while Group II (G2) animals received inorganic bovine bone grafts, and Group III (G3) animals received beta-tricalcium phosphate (beta-TCP) grafts. Clinical evaluation and histomorphometric and immunohistochemical analyses were performed. ANOVA and Tukey's statistical tests were used and a level of significance was considered to be 5%. Results: In the clinical evaluation, animals from G2 and G3 did not present clinical manifestations of osteonecrosis, unlike the control group (G1) animals, which presented necrotic bone tissue exposure in all samples. In the histomorphometric evaluation, animals in G3 showed greater formation of bone tissue (66%) and less formation of bone lacuna (18%) than animals in G1 (58%/32%) and in G2 (59%/27%) (P < 0.05). Moderate (++) immunostaining was observed in G2 and G3 for RANKL, TRAP, and OC, while G1 showed moderate (++) labeling for OC and mild (+) immunostaining for TRAP and RANKL. Conclusions: Greater formation of bone tissue and fewer bone lacunae were found in animals treated with beta-TCP. In clinical evaluation, bone graft groups presented with the clinical manifestation of MRONJ and showed higher intensity of immunostaining for TRAP and RANKL. Despite the limitations of experimental animal studies, the results of this work may assist in the development of future clinical research for the prevention of MRONJ.AOCMF SwitzerlandFundacao Educ Serra Orgaos, Dept Oral & Maxillofacial Surg, Av Alberto Torres 111 Alto, BR-25964004 Teresopolis, RJ, BrazilUniv Fed Fluminense, Dept Oral & Maxillofacial Surg, Nova Friburgo, RJ, BrazilUniv Estadual Paulista, Dept Oral & Maxillofacial Surg, Aracatuba, SP, BrazilSao Paulo Estate Univ, Dept Oral & Maxillofacial Surg, Aracatuba, SP, BrazilUniv Estadual Paulista, Dept Oral & Maxillofacial Surg, Aracatuba, SP, BrazilAOCMF Switzerland: AOCMF-16-02 H.Sage Publications IncFundacao Educ Serra OrgaosUniversidade Federal Fluminense (UFF)Universidade Estadual Paulista (UNESP)Sao Paulo Estate UnivSilva, Jonathan Ribeiro daBalbas, Maria Cristina de MoraesCorrea, Caroline AguedaZanela, ManuellaOkamoto, Roberta [UNESP]Pereira, Rodrigo dos SantosHomsi, NicolasHochuli-Vieira, Eduardo [UNESP]2022-04-28T17:22:35Z2022-04-28T17:22:35Z2021-10-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article8http://dx.doi.org/10.1177/19433875211048367Craniomaxillofacial Trauma & Reconstruction. Thousand Oaks: Sage Publications Inc, 8 p., 2021.1943-3875http://hdl.handle.net/11449/21870110.1177/19433875211048367WOS:000713698000001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCraniomaxillofacial Trauma & Reconstructioninfo:eu-repo/semantics/openAccess2022-04-28T17:22:35Zoai:repositorio.unesp.br:11449/218701Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:12:16.191156Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
title The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
spellingShingle The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
Silva, Jonathan Ribeiro da
bisphosphonate
osteonecrosis
bone graft
bisphosphonate-associated osteonecrosis of the jaw
rats
Wistar
title_short The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
title_full The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
title_fullStr The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
title_full_unstemmed The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
title_sort The Role of Bone Grafts in Preventing Medication-Related Osteonecrosis of the Jaw: Histomorphometric, Immunohistochemical, and Clinical Evaluation in Animal Model
author Silva, Jonathan Ribeiro da
author_facet Silva, Jonathan Ribeiro da
Balbas, Maria Cristina de Moraes
Correa, Caroline Agueda
Zanela, Manuella
Okamoto, Roberta [UNESP]
Pereira, Rodrigo dos Santos
Homsi, Nicolas
Hochuli-Vieira, Eduardo [UNESP]
author_role author
author2 Balbas, Maria Cristina de Moraes
Correa, Caroline Agueda
Zanela, Manuella
Okamoto, Roberta [UNESP]
Pereira, Rodrigo dos Santos
Homsi, Nicolas
Hochuli-Vieira, Eduardo [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Fundacao Educ Serra Orgaos
Universidade Federal Fluminense (UFF)
Universidade Estadual Paulista (UNESP)
Sao Paulo Estate Univ
dc.contributor.author.fl_str_mv Silva, Jonathan Ribeiro da
Balbas, Maria Cristina de Moraes
Correa, Caroline Agueda
Zanela, Manuella
Okamoto, Roberta [UNESP]
Pereira, Rodrigo dos Santos
Homsi, Nicolas
Hochuli-Vieira, Eduardo [UNESP]
dc.subject.por.fl_str_mv bisphosphonate
osteonecrosis
bone graft
bisphosphonate-associated osteonecrosis of the jaw
rats
Wistar
topic bisphosphonate
osteonecrosis
bone graft
bisphosphonate-associated osteonecrosis of the jaw
rats
Wistar
description Objective: To evaluate the effects of inorganic bovine bone graft (Lumina Bone, Criteria, Brazil) and beta-tricalcium phosphate (beta-TCP) graft (ChronOS, Synthes, Brazil) in rats with the risk of developing post-extraction medication-related osteonecrosis of the jaw (MRONJ). Methods: Eighteen male Wistar rats weighing 350 to 450 g were induced to develop MRONJ using zoledronic acid for 5 weeks. In the sixth week, the right maxillary first molar was extracted. The animals in Group I (G1) did not receive bone grafts after tooth extraction, while Group II (G2) animals received inorganic bovine bone grafts, and Group III (G3) animals received beta-tricalcium phosphate (beta-TCP) grafts. Clinical evaluation and histomorphometric and immunohistochemical analyses were performed. ANOVA and Tukey's statistical tests were used and a level of significance was considered to be 5%. Results: In the clinical evaluation, animals from G2 and G3 did not present clinical manifestations of osteonecrosis, unlike the control group (G1) animals, which presented necrotic bone tissue exposure in all samples. In the histomorphometric evaluation, animals in G3 showed greater formation of bone tissue (66%) and less formation of bone lacuna (18%) than animals in G1 (58%/32%) and in G2 (59%/27%) (P < 0.05). Moderate (++) immunostaining was observed in G2 and G3 for RANKL, TRAP, and OC, while G1 showed moderate (++) labeling for OC and mild (+) immunostaining for TRAP and RANKL. Conclusions: Greater formation of bone tissue and fewer bone lacunae were found in animals treated with beta-TCP. In clinical evaluation, bone graft groups presented with the clinical manifestation of MRONJ and showed higher intensity of immunostaining for TRAP and RANKL. Despite the limitations of experimental animal studies, the results of this work may assist in the development of future clinical research for the prevention of MRONJ.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-30
2022-04-28T17:22:35Z
2022-04-28T17:22:35Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1177/19433875211048367
Craniomaxillofacial Trauma & Reconstruction. Thousand Oaks: Sage Publications Inc, 8 p., 2021.
1943-3875
http://hdl.handle.net/11449/218701
10.1177/19433875211048367
WOS:000713698000001
url http://dx.doi.org/10.1177/19433875211048367
http://hdl.handle.net/11449/218701
identifier_str_mv Craniomaxillofacial Trauma & Reconstruction. Thousand Oaks: Sage Publications Inc, 8 p., 2021.
1943-3875
10.1177/19433875211048367
WOS:000713698000001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Craniomaxillofacial Trauma & Reconstruction
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 8
dc.publisher.none.fl_str_mv Sage Publications Inc
publisher.none.fl_str_mv Sage Publications Inc
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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