Is bone transplantation the gold standard for repair of alveolar bone defects?

Detalhes bibliográficos
Autor(a) principal: Raposo-Amaral, Cassio Eduardo
Data de Publicação: 2014
Outros Autores: Bueno, Daniela Franco, Almeida, Ana Beatriz, Jorgetti, Vanda, Costa, Cristiane Cabral, Gouveia, Cecília Helena, Vulcano, Luiz Carlos [UNESP], Fanganiello, Roberto D., Passos-Bueno, Maria Rita, Alonso, Nivaldo
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1177/2041731413519352
http://hdl.handle.net/11449/131031
Resumo: New strategies to fulfill craniofacial bone defects have gained attention in recent years due to the morbidity of autologous bone graft harvesting. We aimed to evaluate the in vivo efficacy of bone tissue engineering strategy using mesenchymal stem cells associated with two matrices (bovine bone mineral and α-tricalcium phosphate), compared to an autologous bone transfer. A total of 28 adult, male, non-immunosuppressed Wistar rats underwent a critical-sized osseous defect of 5 mm diameter in the alveolar region. Animals were divided into five groups. Group 1 (n = 7) defects were repaired with autogenous bone grafts; Group 2 (n = 5) defects were repaired with bovine bone mineral free of cells; Group 3 (n = 5) defects were repaired with bovine bone mineral loaded with mesenchymal stem cells; Group 4 (n = 5) defects were repaired with α-tricalcium phosphate free of cells; and Group 5 (n = 6) defects were repaired with α-tricalcium phosphate loaded with mesenchymal stem cells. Groups 2-5 were compared to Group 1, the reference group. Healing response was evaluated by histomorphometry and computerized tomography. Histomorphometrically, Group 1 showed 60.27% ± 16.13% of bone in the defect. Groups 2 and 3 showed 23.02% ± 8.6% (p = 0.01) and 38.35% ± 19.59% (p = 0.06) of bone in the defect, respectively. Groups 4 and 5 showed 51.48% ± 11.7% (p = 0.30) and 61.80% ± 2.14% (p = 0.88) of bone in the defect, respectively. Animals whose bone defects were repaired with α-tricalcium phosphate and mesenchymal stem cells presented the highest bone volume filling the defects; both were not statistically different from autogenous bone.
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spelling Is bone transplantation the gold standard for repair of alveolar bone defects?Stem cellAlveolar defectBiomaterialBoneBone tissue engineeringOsseous defectΑ-tricalcium phosphateNew strategies to fulfill craniofacial bone defects have gained attention in recent years due to the morbidity of autologous bone graft harvesting. We aimed to evaluate the in vivo efficacy of bone tissue engineering strategy using mesenchymal stem cells associated with two matrices (bovine bone mineral and α-tricalcium phosphate), compared to an autologous bone transfer. A total of 28 adult, male, non-immunosuppressed Wistar rats underwent a critical-sized osseous defect of 5 mm diameter in the alveolar region. Animals were divided into five groups. Group 1 (n = 7) defects were repaired with autogenous bone grafts; Group 2 (n = 5) defects were repaired with bovine bone mineral free of cells; Group 3 (n = 5) defects were repaired with bovine bone mineral loaded with mesenchymal stem cells; Group 4 (n = 5) defects were repaired with α-tricalcium phosphate free of cells; and Group 5 (n = 6) defects were repaired with α-tricalcium phosphate loaded with mesenchymal stem cells. Groups 2-5 were compared to Group 1, the reference group. Healing response was evaluated by histomorphometry and computerized tomography. Histomorphometrically, Group 1 showed 60.27% ± 16.13% of bone in the defect. Groups 2 and 3 showed 23.02% ± 8.6% (p = 0.01) and 38.35% ± 19.59% (p = 0.06) of bone in the defect, respectively. Groups 4 and 5 showed 51.48% ± 11.7% (p = 0.30) and 61.80% ± 2.14% (p = 0.88) of bone in the defect, respectively. Animals whose bone defects were repaired with α-tricalcium phosphate and mesenchymal stem cells presented the highest bone volume filling the defects; both were not statistically different from autogenous bone.Departamento de Cirurgia Plástica e Queimaduras, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, Brazil.Centro de Estudos do Genoma Humano, Instituto de Biociências, Universidade de São Paulo (USP), São Paulo, Brazil.Departamento de Clínica Médica, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, Brazil.Faculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP), São Paulo, Brazil.Faculdade de Medicina Veterinária e Zootecnia, Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP), São Paulo, Brazil.Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Raposo-Amaral, Cassio EduardoBueno, Daniela FrancoAlmeida, Ana BeatrizJorgetti, VandaCosta, Cristiane CabralGouveia, Cecília HelenaVulcano, Luiz Carlos [UNESP]Fanganiello, Roberto D.Passos-Bueno, Maria RitaAlonso, Nivaldo2015-12-07T15:31:01Z2015-12-07T15:31:01Z2014info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1-11application/pdfhttp://dx.doi.org/10.1177/2041731413519352Journal Of Tissue Engineering, v. 5, p. 1-11, 2014.2041-7314http://hdl.handle.net/11449/13103110.1177/2041731413519352PMC3924878.pdf9790998212635563406510501462575324551445PMC3924878PubMedreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal Of Tissue Engineering5.789info:eu-repo/semantics/openAccess2024-09-09T14:05:42Zoai:repositorio.unesp.br:11449/131031Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-09T14:05:42Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Is bone transplantation the gold standard for repair of alveolar bone defects?
title Is bone transplantation the gold standard for repair of alveolar bone defects?
spellingShingle Is bone transplantation the gold standard for repair of alveolar bone defects?
Raposo-Amaral, Cassio Eduardo
Stem cell
Alveolar defect
Biomaterial
Bone
Bone tissue engineering
Osseous defect
Α-tricalcium phosphate
title_short Is bone transplantation the gold standard for repair of alveolar bone defects?
title_full Is bone transplantation the gold standard for repair of alveolar bone defects?
title_fullStr Is bone transplantation the gold standard for repair of alveolar bone defects?
title_full_unstemmed Is bone transplantation the gold standard for repair of alveolar bone defects?
title_sort Is bone transplantation the gold standard for repair of alveolar bone defects?
author Raposo-Amaral, Cassio Eduardo
author_facet Raposo-Amaral, Cassio Eduardo
Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos [UNESP]
Fanganiello, Roberto D.
Passos-Bueno, Maria Rita
Alonso, Nivaldo
author_role author
author2 Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos [UNESP]
Fanganiello, Roberto D.
Passos-Bueno, Maria Rita
Alonso, Nivaldo
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Raposo-Amaral, Cassio Eduardo
Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos [UNESP]
Fanganiello, Roberto D.
Passos-Bueno, Maria Rita
Alonso, Nivaldo
dc.subject.por.fl_str_mv Stem cell
Alveolar defect
Biomaterial
Bone
Bone tissue engineering
Osseous defect
Α-tricalcium phosphate
topic Stem cell
Alveolar defect
Biomaterial
Bone
Bone tissue engineering
Osseous defect
Α-tricalcium phosphate
description New strategies to fulfill craniofacial bone defects have gained attention in recent years due to the morbidity of autologous bone graft harvesting. We aimed to evaluate the in vivo efficacy of bone tissue engineering strategy using mesenchymal stem cells associated with two matrices (bovine bone mineral and α-tricalcium phosphate), compared to an autologous bone transfer. A total of 28 adult, male, non-immunosuppressed Wistar rats underwent a critical-sized osseous defect of 5 mm diameter in the alveolar region. Animals were divided into five groups. Group 1 (n = 7) defects were repaired with autogenous bone grafts; Group 2 (n = 5) defects were repaired with bovine bone mineral free of cells; Group 3 (n = 5) defects were repaired with bovine bone mineral loaded with mesenchymal stem cells; Group 4 (n = 5) defects were repaired with α-tricalcium phosphate free of cells; and Group 5 (n = 6) defects were repaired with α-tricalcium phosphate loaded with mesenchymal stem cells. Groups 2-5 were compared to Group 1, the reference group. Healing response was evaluated by histomorphometry and computerized tomography. Histomorphometrically, Group 1 showed 60.27% ± 16.13% of bone in the defect. Groups 2 and 3 showed 23.02% ± 8.6% (p = 0.01) and 38.35% ± 19.59% (p = 0.06) of bone in the defect, respectively. Groups 4 and 5 showed 51.48% ± 11.7% (p = 0.30) and 61.80% ± 2.14% (p = 0.88) of bone in the defect, respectively. Animals whose bone defects were repaired with α-tricalcium phosphate and mesenchymal stem cells presented the highest bone volume filling the defects; both were not statistically different from autogenous bone.
publishDate 2014
dc.date.none.fl_str_mv 2014
2015-12-07T15:31:01Z
2015-12-07T15:31:01Z
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/10.1177/2041731413519352
Journal Of Tissue Engineering, v. 5, p. 1-11, 2014.
2041-7314
http://hdl.handle.net/11449/131031
10.1177/2041731413519352
PMC3924878.pdf
9790998212635563
4065105014625753
24551445
PMC3924878
url http://dx.doi.org/10.1177/2041731413519352
http://hdl.handle.net/11449/131031
identifier_str_mv Journal Of Tissue Engineering, v. 5, p. 1-11, 2014.
2041-7314
10.1177/2041731413519352
PMC3924878.pdf
9790998212635563
4065105014625753
24551445
PMC3924878
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal Of Tissue Engineering
5.789
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1-11
application/pdf
dc.source.none.fl_str_mv PubMed
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 repositoriounesp@unesp.br
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