Effect of surgical implantation of recombinant human bone morphogenetic protein-2 in a bioabsorbable collagen sponge or calcium phosphate putty carrier in intrabony periodontal defects in the baboon

被引:38
作者
Blumenthal, NM
Koh-Kunst, G
Alves, MEAF
Miranda, D
Sorensen, RG
Wozney, JM
Wikesjö, UME
机构
[1] Univ Illinois, Coll Dent, Dept Periodontol, Chicago, IL 60612 USA
[2] Wyeth Ayerst Res, Musculoskeletal Sci Bone Biol & Applicat Genet In, Cambridge, MA USA
[3] Temple Univ, Sch Dent, Lab Appl Periodontal & Craniofacial Regenerat, Dept Periodontol, Philadelphia, PA USA
关键词
animal studies; bone regeneration; periodontal attachment; periodontal regeneration; dental cementum/growth and development; proteins; bone morphogenetic; wound healing;
D O I
10.1902/jop.2002.73.12.1494
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: Recombinant human bone morphogenetic protein-2 (rhBMP-2) in a proper carrier has been shown to induce clinically relevant bone formation for several oral/maxillofacial and periodontal indications and to stimulate regeneration of the periodontal attachment. The objective of this study is to evaluate regeneration of alveolar bone, cementum, periodontal ligament, and associated root resorption and ankylosis following surgical implantation of rhBMP-2 in an absorbable Collagen sponge (ACS) or a calcium phosphate putty (alphaBSM) carrier in 3-wall intrabony periodontal defects in the baboon. Methods: rhBMP-2/ACS and rhBMP-2/alphaBSM were implanted in surgically produced, maxillary and mandibular, large size, 3-wall intrabony defects in 4 baboons. Contralateral jaw quadrants were implanted with buffer/ACS, buffer/ alphaBSM, or served as sham-operated surgical controls. Treatments were allocated to left and right, maxillary and mandibular, jaw quadrants following a randomization schedule. Four months following implantation, block biopsies of defect sites were obtained, processed, and subjected to histologic and histometric analysis. Results: Defect sites receiving rhBMP-2/ACS and rhBMP-2/alphaBSM demonstrated significantly greater regeneration than controls. No significant differences were observed between defect sites receiving rhBMP-2/ACS or rhBMP-2/alphaBSM regarding epithelial migration and connective tissue attachment and new bone formation. However, rhBMP-2/ACS supported significantly greater new cementum formation. Ankylosis or root resorption were not observed. Conclusions: The results of this study support the use of rhBMP-2 to enhance periodontal regeneration of intrabony periodontal defects. While this novel technology holds promise, refinement in carrier systems may provide the key to enhancement of the regenerative potential.
引用
收藏
页码:1494 / 1506
页数:13
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