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Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects
CONTEXT: Bone morphogenetic proteins (BMP) are multifunctional molecules of transforming growth factor-β superfamily that induces the differentiation of fibroblasts into osteoblasts to form bone. AIMS: This study was undertaken to evaluate the effects of recombinant human BMP-7 (rhBMP-7) in bone hea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714274/ https://www.ncbi.nlm.nih.gov/pubmed/31516225 http://dx.doi.org/10.4103/jomfp.JOMFP_292_18 |
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author | Anand, Vaibhav Vignesh, U Mehrotra, Divya Kumar, Sumit |
author_facet | Anand, Vaibhav Vignesh, U Mehrotra, Divya Kumar, Sumit |
author_sort | Anand, Vaibhav |
collection | PubMed |
description | CONTEXT: Bone morphogenetic proteins (BMP) are multifunctional molecules of transforming growth factor-β superfamily that induces the differentiation of fibroblasts into osteoblasts to form bone. AIMS: This study was undertaken to evaluate the effects of recombinant human BMP-7 (rhBMP-7) in bone healing of small maxillofacial bone defects and assess the serum levels of osteopontin (OPN) and receptor activator of nuclear factor kappa-B ligand (RANKL) biomarkers for bone remodeling. MATERIALS AND METHODS: Twenty patients with small maxillofacial bony defects were enrolled in this study and randomly allocated to two groups; wherein after apicoectomy of the involved teeth, the control group had defect filled with collagen sponge only while the experimental group had rhBMP-7 impregnated collagen sponge placed in the defect. RESULTS: The clinical parameters showed no significant difference between the two groups (P > 0.05). The radiographic parameters showed a significantly slower rate of reduction in bone defect volume (P < 0.01) in control group than the experimental group when followed at 2, 4 and 24 postoperative weeks. RANKL and OPN serum levels showed no significant changes in pre- and post-operative stage. CONCLUSION: This study confirms that rhBMP-7 in collagen definitely accelerates bone healing in maxillofacial bone defects and minimizes postoperative complications. RANKL and OPN biomarkers in serum may not show bone remodeling, hence tissue samples may be used to assess their levels. |
format | Online Article Text |
id | pubmed-6714274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-67142742019-09-12 Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects Anand, Vaibhav Vignesh, U Mehrotra, Divya Kumar, Sumit J Oral Maxillofac Pathol Original Article CONTEXT: Bone morphogenetic proteins (BMP) are multifunctional molecules of transforming growth factor-β superfamily that induces the differentiation of fibroblasts into osteoblasts to form bone. AIMS: This study was undertaken to evaluate the effects of recombinant human BMP-7 (rhBMP-7) in bone healing of small maxillofacial bone defects and assess the serum levels of osteopontin (OPN) and receptor activator of nuclear factor kappa-B ligand (RANKL) biomarkers for bone remodeling. MATERIALS AND METHODS: Twenty patients with small maxillofacial bony defects were enrolled in this study and randomly allocated to two groups; wherein after apicoectomy of the involved teeth, the control group had defect filled with collagen sponge only while the experimental group had rhBMP-7 impregnated collagen sponge placed in the defect. RESULTS: The clinical parameters showed no significant difference between the two groups (P > 0.05). The radiographic parameters showed a significantly slower rate of reduction in bone defect volume (P < 0.01) in control group than the experimental group when followed at 2, 4 and 24 postoperative weeks. RANKL and OPN serum levels showed no significant changes in pre- and post-operative stage. CONCLUSION: This study confirms that rhBMP-7 in collagen definitely accelerates bone healing in maxillofacial bone defects and minimizes postoperative complications. RANKL and OPN biomarkers in serum may not show bone remodeling, hence tissue samples may be used to assess their levels. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6714274/ /pubmed/31516225 http://dx.doi.org/10.4103/jomfp.JOMFP_292_18 Text en Copyright: © 2019 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Anand, Vaibhav Vignesh, U Mehrotra, Divya Kumar, Sumit Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title | Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title_full | Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title_fullStr | Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title_full_unstemmed | Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title_short | Evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
title_sort | evaluation of bone formation using recombinant human bone morphogenetic proteins-7 in small maxillofacial bony defects |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714274/ https://www.ncbi.nlm.nih.gov/pubmed/31516225 http://dx.doi.org/10.4103/jomfp.JOMFP_292_18 |
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