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Bone formation at recombinant human bone morphogenetic protein-2-coated titanium implants in the posterior mandible (Type II bone) in dogs

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dc.contributor.authorWikesjö, UM-
dc.contributor.authorXiropaidis, AV-
dc.contributor.authorQahash, M-
dc.contributor.authorLim, Won Hee-
dc.contributor.authorSorensen, RG-
dc.contributor.authorRohrer, MD-
dc.contributor.authorWozney, JM-
dc.contributor.authorHall, J.-
dc.date.accessioned2010-09-09T05:52:30Z-
dc.date.available2010-09-09T05:52:30Z-
dc.date.issued2008-11-
dc.identifier.citationJ Clin Periodontol. 35(11), 985-991en
dc.identifier.issn0303-6979-
dc.identifier.urihttps://hdl.handle.net/10371/69777-
dc.description.abstractBACKGROUND: Conventional oral/maxillofacial implants reach osseointegration over several months during which the titanium fixtures interact with alveolar bone. The objective of this study was to determine if adsorbing recombinant human bone morphogenetic protein-2 (rhBMP-2) onto a titanium porous oxide (TPO) implant surface might enhance or accelerate local bone formation and support osseointegration in a large animal oral/maxillofacial orthotopic model. MATERIAL AND METHODS: Endosseous implants with a TPO surface were installed into the edentulated posterior mandible in eight adult Hound Labrador mongrel dogs. The implant surface had been adsorbed with rhBMP-2 at 0.2 or 4.0 mg/ml. TPO implants without rhBMP-2 served as control. Treatments were randomized between jaw quadrants. Mucosal flaps were advanced and sutured leaving the implants submerged. Clinical and radiographic evaluations were made immediately post-surgery, at day 10 (suture removal), and week 4 and 8 post-surgery. The animals received fluorescent bone markers at week 3, 4, and at week 8 post-surgery, when they were euthanized for histologic analysis. RESULTS: TPO implants coated with rhBMP-2 exhibited dose-dependent bone remodelling including immediate resorption and formation of implant adjacent bone, and early establishment of clinically relevant osseointegration. The resulting bone-implant contact, although clinically respectable, appeared significantly lower for rhBMP-2-coated implants compared with the control [rhBMP-2 (0.2 mg/ml) 43.3+/-10.8%versus 71.7+/-7.8%, p<0.02; rhBMP-2 (4.0 mg/ml) 35.4+/-10.6%versus 68.2+/-11.0%, p<0.03]. CONCLUSIONS: rhBMP-2 adsorbed onto TPO implant surfaces initiates dose-dependent peri-implant bone re-modelling resulting in the formation of normal, physiologic bone and clinically relevant osseointegration within 8 weeks.en
dc.description.sponsorshipThis study was supported by a grant from
Wyeth Research, Cambridge, MA, USA,
and Nobel Biocare AB, Go¨teborg, Sweden.
Jan Hall is an employee of Nobel Biocare
AB. Rachel G. Sorensen was an employee
of Wyeth Research at the time of study.
John Wozney is an employee of Wyeth
Research. Ulf M. E. Wikesjo¨ was an
employee of Wyeth Research, and presently
serves as consultant to Wyeth
Research and Nobel Biocare AB.
en
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.subjectbone morphogenetic proteinen
dc.subjectdental/oral implantsen
dc.subjectdogsen
dc.subjectosseointegrationen
dc.subjectporous titanium oxideen
dc.subjectrhBMP-2en
dc.subjecttissue engineeringen
dc.subjecttitaniumen
dc.titleBone formation at recombinant human bone morphogenetic protein-2-coated titanium implants in the posterior mandible (Type II bone) in dogsen
dc.typeArticleen
dc.contributor.AlternativeAuthor임원희-
dc.identifier.doi10.1111/j.1600-051X.2008.01318.x.-
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