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Article: Effect of recombinant human bone morphogenetic protein-2 on mandibular distraction at different rates in an experimental model
Title | Effect of recombinant human bone morphogenetic protein-2 on mandibular distraction at different rates in an experimental model |
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Authors | |
Keywords | Distraction osteogenesis Mandible Rabbit Recombinant human bone morphogenetic protein-2 |
Issue Date | 2006 |
Publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://www.jcraniofacialsurgery.com |
Citation | Journal Of Craniofacial Surgery, 2006, v. 17 n. 1, p. 100-108 How to Cite? |
Abstract | This study evaluates the effect of recombinant human (rh) bone morphogenetic protein (BMP)-2 on mandibular distraction at normal and rapid distraction rates. This study also determines the feasibility of compensating for the increased distraction rate by the addition of rhBMP-2 while maintaining the quality of the distraction regenerate. Twenty-four New Zealand white rabbits were divided into 2 groups, 1 treated at a normal distraction rate (0.9 mm/d) and the other at a rapid distraction rate (2.7 mm/d). At the end of the active distraction period, rhBMP-2 was injected into distraction regenerate, and the contralateral side was used as a control. The distraction regenerates were analyzed by plain radiography, microcomputed tomography, and mechanical testing. The results showed that rhBMP-2 can promote bone formation at both rapid and normal distraction rates. At week 2 and week 4 of consolidation, bone volumes in the BMP-injection sides were significantly higher than in the control sides, but no statistically significant difference was observed between the BMP-injection sides of the rapid and normal distraction groups. At week 8 of consolidation, mechanical testing demonstrated no significant difference of the failure load and stiffness between the BMP-injection and control sides. In conclusion, the study indicates that rhBMP-2 can enhance bone ossification at both normal and rapid distraction rates. The addition of rhBMP-2 can compensate for the rapid distraction rate in mandibular distraction osteogenesis. However, in the long term, the bone quality and stiffness of the distraction regeneration was not influenced by rhBMP-2. Copyright © Mutaz B. Habal, MD. |
Persistent Identifier | http://hdl.handle.net/10722/90706 |
ISSN | 2023 Impact Factor: 1.0 2023 SCImago Journal Rankings: 0.420 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Cheung, LK | en_HK |
dc.contributor.author | Zheng, LW | en_HK |
dc.date.accessioned | 2010-09-17T10:07:05Z | - |
dc.date.available | 2010-09-17T10:07:05Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Journal Of Craniofacial Surgery, 2006, v. 17 n. 1, p. 100-108 | en_HK |
dc.identifier.issn | 1049-2275 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/90706 | - |
dc.description.abstract | This study evaluates the effect of recombinant human (rh) bone morphogenetic protein (BMP)-2 on mandibular distraction at normal and rapid distraction rates. This study also determines the feasibility of compensating for the increased distraction rate by the addition of rhBMP-2 while maintaining the quality of the distraction regenerate. Twenty-four New Zealand white rabbits were divided into 2 groups, 1 treated at a normal distraction rate (0.9 mm/d) and the other at a rapid distraction rate (2.7 mm/d). At the end of the active distraction period, rhBMP-2 was injected into distraction regenerate, and the contralateral side was used as a control. The distraction regenerates were analyzed by plain radiography, microcomputed tomography, and mechanical testing. The results showed that rhBMP-2 can promote bone formation at both rapid and normal distraction rates. At week 2 and week 4 of consolidation, bone volumes in the BMP-injection sides were significantly higher than in the control sides, but no statistically significant difference was observed between the BMP-injection sides of the rapid and normal distraction groups. At week 8 of consolidation, mechanical testing demonstrated no significant difference of the failure load and stiffness between the BMP-injection and control sides. In conclusion, the study indicates that rhBMP-2 can enhance bone ossification at both normal and rapid distraction rates. The addition of rhBMP-2 can compensate for the rapid distraction rate in mandibular distraction osteogenesis. However, in the long term, the bone quality and stiffness of the distraction regeneration was not influenced by rhBMP-2. Copyright © Mutaz B. Habal, MD. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Lippincott Williams & Wilkins. The Journal's web site is located at http://www.jcraniofacialsurgery.com | en_HK |
dc.relation.ispartof | Journal of Craniofacial Surgery | en_HK |
dc.subject | Distraction osteogenesis | en_HK |
dc.subject | Mandible | en_HK |
dc.subject | Rabbit | en_HK |
dc.subject | Recombinant human bone morphogenetic protein-2 | en_HK |
dc.title | Effect of recombinant human bone morphogenetic protein-2 on mandibular distraction at different rates in an experimental model | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Cheung, LK:lkcheung@hkucc.hku.hk | en_HK |
dc.identifier.email | Zheng, LW:lwzheng@hku.hk | en_HK |
dc.identifier.authority | Cheung, LK=rp00013 | en_HK |
dc.identifier.authority | Zheng, LW=rp01411 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1097/01.scs.0000188744.06723.1f | en_HK |
dc.identifier.scopus | eid_2-s2.0-33645807396 | en_HK |
dc.identifier.hkuros | 114008 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33645807396&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 17 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 100 | en_HK |
dc.identifier.epage | 108 | en_HK |
dc.identifier.isi | WOS:000235065900021 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Cheung, LK=7102302747 | en_HK |
dc.identifier.scopusauthorid | Zheng, LW=11241247300 | en_HK |
dc.identifier.issnl | 1049-2275 | - |