De novo bone induction by recombinant human bone morphogenetic protein-2 (rhBMP-2) in maxillary sinus floor augmentation

被引:267
作者
Boyne, PJ
Lilly, LC
Marx, RE
Moy, PK
Nevins, M
Spagnoli, DB
Triplett, RG
机构
[1] Loma Linda Univ, Med Ctr, Dept Surg, Oral & Maxillofacial Surg Serv, Loma Linda, CA 92350 USA
[2] Wyeth Ayerst Res, Clin Trial Operat, Cambridge, MA USA
[3] Univ Miami, Miller Sch Med, Div Oral & Maxillofacial Surg, Miami, FL 33152 USA
[4] Univ Calif Los Angeles, Los Angeles, CA 90024 USA
[5] Harvard Univ, Sch Dent Med, Swampscott, MA USA
[6] Univ Oral & Maxillofacial Surg, Charlotte, NC USA
[7] Texas A&M Univ Syst, Baylor Coll Dent, Hlth Sci Ctr, Dallas, TX USA
关键词
D O I
10.1016/j.joms.2005.08.018
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: This phase 11 study was designed to evaluate 2 concentrations of recombinant human bone morphogenetic protein-2 (rhBMP-2) for safety and efficacy in inducing adequate bone for endosseous dental implant in patients requiring staged maxillary sinus floor augmentation. Materials and Methods: Patients were treated with rhBMP-2 (via an absorbable collagen sponge [ACS]), at concentrations of 0.75 mg/mL (n = 18), 1.50 mg/mL (n = 17), or with bone graft (n = 13). Bone induction was assessed by alveolar ridge height, width, and density measurements from computed tomography scans obtained before and 4 months after treatment and 6 months post-functional loading of dental implants (density only). Results: Mean increases in alveolar ridge height at 4 months after treatment were similar among the groups; 11.3 mm, 9.5 mm, and 10.2 mm, respectively, in the bone graft, 0.75 mg/mL, and 1.50 mg/mL rhBMP-2/ACS treatment groups. Mean increases in alveolar ridge width (buccal to lingual) at the crest of the ridge were statistically different among the treatment groups; 4.7 mm, 2.0 mm, and 2.0 mm, respectively, in the bone graft, 0.75 mg/mL, and 1.50 mg/mL treatment groups (P <= .01 vs 0.75 mg/mL; P < .01 vs 1.50 mg/mL). At 4 months postoperative new bone density was statistically different among the treatment groups; 350 mg/cc, 84 mg/cc, and 134 mg/cc for the bone graft, 0.75 mg/mL, and 1.50 mg/mL rhBMP-2/ACS treatment groups, respectively (P = .003 vs 0.75 mg/mL, P = .0137 vs 1.50 mg/mL, P = .0188; 1.50 mg/niL vs 0.75 mg/mL). Core bone biopsies obtained at the time of dental implant placement confirmed normal bone formation. The proportion of patients who received dental implants that were functionally loaded and remained functional at 36 months post-functional loading was 62%, 67%, and 76% in the bone graft, 0.75 mg/mL, and 1.50 mg/mL rhBMP-2/ACS treatment groups, respectively. Conclusion: This study is the first randomized controlled trial demonstrating de novo organ tissue growth in humans from a recombinant human protein. rhBMP-2/ACS safely induced adequate bone for the placement and functional loading of endosseous dental implants in patients requiring staged maxillary sinus floor augmentation. (c) 2005 American Association of Oral and Maxillofacial Surgeons.
引用
收藏
页码:1693 / 1707
页数:15
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