Bone morphogenetic proteins for periodontal and alveolar indications; biological observations – clinical implications
Article first published online: 13 JUL 2009
DOI: 10.1111/j.1601-6343.2009.01461.x
Copyright © 2009 The Authors. Journal compilation © 2009 John Wiley & Sons A/S
Issue

Orthodontics & Craniofacial Research
Special Issue: Proceedings of the Fourth Biennial Conference: Biomedicine in Orthodontics - From Tooth Movement to Facial Growth
Volume 12, Issue 3, pages 263–270, August 2009
Additional Information
How to Cite
Wikesjö, U., Qahash, M., Huang, Y.-H., Xiropaidis, A., Polimeni, G. and Susin, C. (2009), Bone morphogenetic proteins for periodontal and alveolar indications; biological observations – clinical implications. Orthodontics & Craniofacial Research, 12: 263–270. doi: 10.1111/j.1601-6343.2009.01461.x
Publication History
- Issue published online: 13 JUL 2009
- Article first published online: 13 JUL 2009
- Dates: Accepted 11 March 2009
- Abstract
- Article
- References
- Cited By
Keywords:
- bone formation;
- bone morphogenetic protein;
- osseointegration;
- tissue engineering;
- titanium implants
Structured Abstract
Authors – Wikesjö UME, Qahash M, Huang Y-H, Xiropaidis A, Polimeni G, Susin C
Surgical placement of endosseous oral implants is governed by the prosthetic design and by the morphology and quality of the alveolar bone. Nevertheless, often implant placement may be complexed, if at all possible, by alveolar ridge irregularities resulting from periodontal disease, and chronic and acute trauma. In consequence, implant positioning commonly necessitates bone augmentation procedures. One objective of our laboratory is to evaluate the biologic potential of bone morphogenetic proteins (BMP) and other candidate biologics, bone biomaterials, and devices for alveolar ridge augmentation and implant fixation using discriminating large animal models. This focused review illustrates the unique biologic potential, the clinical relevance and perspectives of recombinant human BMP-2 (rhBMP-2) using a variety of carrier technologies to induce local bone formation and implant osseointegration for inlay and onlay indications. Our studies demonstrate a clinically relevant potential of a purpose-designed titanium porous oxide implant surface as stand-alone technology to deliver rhBMP-2 for alveolar augmentation. In perspective, merits and shortcomings of current treatment protocol including bone biomaterials and guided bone regeneration are addressed and explained. We demonstrate that rhBMP-2 has unparalleled potential to augment alveolar bone, and support implant osseointegration and long-term functional loading. Inclusion of rhBMP-2 for alveolar augmentation and osseointegration will not only enhance predictability of existing clinical protocol but also radically change current treatment paradigms.

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