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

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 min...

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Autores principales: Raposo-Amaral, Cassio Eduardo, Bueno, Daniela Franco, Almeida, Ana Beatriz, Jorgetti, Vanda, Costa, Cristiane Cabral, Gouveia, Cecília Helena, Vulcano, Luiz Carlos, Fanganiello, Roberto D, Passos-Bueno, Maria Rita, Alonso, Nivaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924878/
https://www.ncbi.nlm.nih.gov/pubmed/24551445
http://dx.doi.org/10.1177/2041731413519352
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author Raposo-Amaral, Cassio Eduardo
Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos
Fanganiello, Roberto D
Passos-Bueno, Maria Rita
Alonso, Nivaldo
author_facet Raposo-Amaral, Cassio Eduardo
Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos
Fanganiello, Roberto D
Passos-Bueno, Maria Rita
Alonso, Nivaldo
author_sort Raposo-Amaral, Cassio Eduardo
collection PubMed
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.
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spelling pubmed-39248782014-02-18 Is bone transplantation the gold standard for repair of alveolar bone defects? Raposo-Amaral, Cassio Eduardo Bueno, Daniela Franco Almeida, Ana Beatriz Jorgetti, Vanda Costa, Cristiane Cabral Gouveia, Cecília Helena Vulcano, Luiz Carlos Fanganiello, Roberto D Passos-Bueno, Maria Rita Alonso, Nivaldo J Tissue Eng Article 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. SAGE Publications 2014-01-17 /pmc/articles/PMC3924878/ /pubmed/24551445 http://dx.doi.org/10.1177/2041731413519352 Text en © The Author(s) 2014
spellingShingle Article
Raposo-Amaral, Cassio Eduardo
Bueno, Daniela Franco
Almeida, Ana Beatriz
Jorgetti, Vanda
Costa, Cristiane Cabral
Gouveia, Cecília Helena
Vulcano, Luiz Carlos
Fanganiello, Roberto D
Passos-Bueno, Maria Rita
Alonso, Nivaldo
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?
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_short 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?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924878/
https://www.ncbi.nlm.nih.gov/pubmed/24551445
http://dx.doi.org/10.1177/2041731413519352
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