TY - JOUR
T1 - The impact of alloplast and allograft on bone homeostasis
T2 - Orthodontic tooth movement into regenerated bone
AU - Klein, Yehuda
AU - Kunthawong, Natthapong
AU - Fleissig, Omer
AU - Casap, Nardi
AU - Polak, David
AU - Chaushu, Stella
N1 - Publisher Copyright:
© 2019 American Academy of Periodontology
PY - 2020/8/1
Y1 - 2020/8/1
N2 - 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.
AB - 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.
KW - bone regeneration
KW - orthodontics
KW - wound healing
UR - http://www.scopus.com/inward/record.url?scp=85082109794&partnerID=8YFLogxK
U2 - 10.1002/JPER.19-0145
DO - 10.1002/JPER.19-0145
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C2 - 31887228
AN - SCOPUS:85082109794
SN - 0022-3492
VL - 91
SP - 1067
EP - 1075
JO - Journal of Periodontology
JF - Journal of Periodontology
IS - 8
ER -