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Research ArticleOriginal Article
Open Access

Recombinant human bone morphogenetic protein-7 and bone marrow as a substitute for bone graft in reconstruction defect of rabbit mandible

Amer Smajilagic, Moustafa Y. Al-Khalil, Amira Redjic, Selma Filipovic, Besima Hadjihasanovic and Sami Lappalainen
Saudi Medical Journal September 2005, 26 (9) 1398-1402;
Amer Smajilagic
Clinic for Maxillofacial Surgery, University Clinic Center Sarajevo, Porodice Ribara 91, Sarajevo, Bosnia and Herzegovina. Tel. +387 (33) 664326. Fax. +387 (33) 664328. E-mail: [email protected]
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Moustafa Y. Al-Khalil
Clinic for Maxillofacial Surgery, University Clinic Center Sarajevo, Sarajevo, Bosnia and Herzegovina.
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Amira Redjic
Institute for Biology and Human Genetic, Medical Faculty, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
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Selma Filipovic
Orthopedic and Ophthalmology (Filipovic) Faculty of Veterinary Medicine, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
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Besima Hadjihasanovic
Institute of Radiology, University Clinic Center Sarajevo, Sarajevo, Bosnia and Herzegovina.
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Sami Lappalainen
Department of Health Sciences, Jyvaskyla, Finland.
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Abstract

OBJECTIVE: To obtain information on the feasibility of employing recombinant human bone morphogenetic protein-7 (rhBMP-7), mixed with bone marrow as a substitute for autologous bone graft.

METHODS: We carried out the study in the University Clinic Center, Sarajevo, Bosnia and Herzegovina, from February 2002 to January 2004. Six New Zealand rabbits underwent hemiresection of the mandible. We placed rhBMP-7 in a concentration of 100 micrograms and collagen (ACS) as carrier mixed with bone marrow in the defects in 3 animals. In another group of 3, we restored the defect by placement of autologous bone graft harvested from the iliac crest. We evaluated the results by the activity of the alkaline phosphatase enzyme (ALP), CT assessment with bone mineral density (BMD) analysis, and clinical and histologic examinations.

RESULTS: The ALP activity was significantly higher after 14 days, in the rhBMP7/ACS sites than the bone graft sites (30th day). Mean BMD of tissue induced by rhBMP-7/ACS on the 30th day was 510 mg/cm3 in caudal, and 553 mg/cm3 in sagittal plane, and bone graft tissue was 510 mg/cm3 in caudal and 530 mg/cm3 in sagittal plane. Clinical inspection and histologic examination on the 60th day showed complete bridged defects with abundant woven bone in 2 of 3 rhBMP-7/ACS sites (67%), and no incorporation of the autologous bone graft into the other groups treated sites.

CONCLUSION: The rhBMP-7/ACS mixed with bone marrow was very effective in establishing complete bone regeneration into the defects, indicating that it could be an adequate alternative for autologous bone transplantation.

  • Copyright: © Saudi Medical Journal

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Saudi Medical Journal: 26 (9)
Saudi Medical Journal
Vol. 26, Issue 9
1 Sep 2005
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Recombinant human bone morphogenetic protein-7 and bone marrow as a substitute for bone graft in reconstruction defect of rabbit mandible
Amer Smajilagic, Moustafa Y. Al-Khalil, Amira Redjic, Selma Filipovic, Besima Hadjihasanovic, Sami Lappalainen
Saudi Medical Journal Sep 2005, 26 (9) 1398-1402;

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Recombinant human bone morphogenetic protein-7 and bone marrow as a substitute for bone graft in reconstruction defect of rabbit mandible
Amer Smajilagic, Moustafa Y. Al-Khalil, Amira Redjic, Selma Filipovic, Besima Hadjihasanovic, Sami Lappalainen
Saudi Medical Journal Sep 2005, 26 (9) 1398-1402;
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© 2025 Saudi Medical Journal Saudi Medical Journal is copyright under the Berne Convention and the International Copyright Convention.  Saudi Medical Journal is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work. Electronic ISSN 1658-3175. Print ISSN 0379-5284.

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