Yehuda Klein1, Natthapong Kunthawong1, Omer Fleissig1, Nardi Casap2, David Polak3, Stella Chaushu1. 1. Department of Orthodontics, Hebrew University-Hadassah Faculty of Dental Medicine, Jerusalem, Israel. 2. Department of Maxillofacial Surgery, Hebrew University-Hadassah Faculty of Dental Medicine, Jerusalem, Israel. 3. Department of Periodontology, Hebrew University-Hadassah Faculty of Dental Medicine, Jerusalem, Israel.
Abstract
BACKGROUND: The aim of the study is to examine bone healing following augmentation with allograft or β-tricalcium phosphate (β-TCP) and evaluate orthodontic tooth movement (OTM) into the augmented sites. METHODS: The study included two parts. Part I included the alveolar bone regeneration model. Osseous defects were created by extraction of the maxillary first molars in C57BL/6 mice, and the sockets were filled with allograft, β-TCP, or left unfilled (n = 6/group). Mouse allograft was prepared by a novel method using long bones. Maxillae were collected at 2, 4, and 6 weeks for microcomputed tomography (μCT) and histological analysis. In Part II, OTM was performed after full bone healing, through grafted and unfilled sockets (n = 10/group), and the second molar shift was assessed using μCT. RESULTS: Bone volume and trabeculation were reduced in β-TCP compared with allograft and non-grafted groups at 2 and 4 weeks post-grafting, but similar at 6 weeks. Graft particles could be detected at 2 weeks post-grafting for β-TCP, and at 2 and 4 weeks for allograft. Increased osteoclasts' presence was observed in the β-TCP group at 2 and 4 weeks compared with allograft and control. OTM was similar in the two graft groups, but impaired versus the non-grafted controls. CONCLUSION: β-TCP and allograft induce full normal healing but alter OTM into the regenerated sites.
BACKGROUND: The aim of the study is to examine bone healing following augmentation with allograft or β-tricalcium phosphate (β-TCP) and evaluate orthodontic tooth movement (OTM) into the augmented sites. METHODS: The study included two parts. Part I included the alveolar bone regeneration model. Osseous defects were created by extraction of the maxillary first molars in C57BL/6 mice, and the sockets were filled with allograft, β-TCP, or left unfilled (n = 6/group). Mouse allograft was prepared by a novel method using long bones. Maxillae were collected at 2, 4, and 6 weeks for microcomputed tomography (μCT) and histological analysis. In Part II, OTM was performed after full bone healing, through grafted and unfilled sockets (n = 10/group), and the second molar shift was assessed using μCT. RESULTS: Bone volume and trabeculation were reduced in β-TCP compared with allograft and non-grafted groups at 2 and 4 weeks post-grafting, but similar at 6 weeks. Graft particles could be detected at 2 weeks post-grafting for β-TCP, and at 2 and 4 weeks for allograft. Increased osteoclasts' presence was observed in the β-TCP group at 2 and 4 weeks compared with allograft and control. OTM was similar in the two graft groups, but impaired versus the non-grafted controls. CONCLUSION: β-TCP and allograft induce full normal healing but alter OTM into the regenerated sites.