Transsutural distraction and tissue regeneration of the midfacial skeleton: experimental studies in growing dogs

Cleft Palate Craniofac J. 2014 May;51(3):326-33. doi: 10.1597/12-056. Epub 2013 Jan 31.

Abstract

Objective : The purpose of this study was to evaluate the effect of different mechanical forces on the expansion of the palatine suture using transsutural distraction osteogenesis. Methods : A total of 48 dogs were used in this study. The experimental groups were treated with a custom-designed internal distractor. Bone regeneration was determined with x-rays and histology. The computed values underwent statistical analyses using analysis of variance. Results : The maxillary complex was most noticeably advanced with an applied mechanical force of 600 g (20.15 ± 1.36 mm), compared with forces of 400 g (19.88 ± 1.41 mm) and 800 g (2.24 ± 0.93 mm). Immunohistochemical staining showed that the expression of bone morphogenetic protein-2 and bone morphogenetic protein-4 fluctuated with different mechanical forces. These changes were statistically significant when 600 g of force was applied within 30 days of distraction (P < .05). Conclusions : Transsutural distraction osteogenesis in the growing dog should be safe and well tolerated in inducing bony lengthening of the maxilla, and the optimal force is 600 × g. Bone morphogenetic protein-2 and bone morphogenetic protein-4 may play an important roles in the signaling pathways that link mechanical forces and biological responses.

Keywords: BMPs; bone regeneration; midfacial hypoplasia; transsutural distraction osteogenesis.

MeSH terms

  • Animals
  • Biomechanical Phenomena
  • Bone Morphogenetic Protein 2 / metabolism
  • Bone Morphogenetic Protein 4 / metabolism
  • Bone Regeneration / physiology*
  • Bone Remodeling / physiology
  • Cranial Sutures / surgery*
  • Dogs
  • Equipment Design
  • Immunohistochemistry
  • Models, Animal
  • Osteogenesis, Distraction / instrumentation
  • Osteogenesis, Distraction / methods*

Substances

  • Bone Morphogenetic Protein 2
  • Bone Morphogenetic Protein 4