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Computed Tomography and Optical Imaging of Osteogenesis-angiogenesis Coupling to Assess Integration of Cranial Bone Autografts and Allografts
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Optimizing autologous bone contribution to implant osseointegration.

Benjamin R Coyac1, Qiang Sun1,2, Brian Leahy1

  • 1Department of Plastic and Reconstructive Surgery, School of Medicine, Stanford University, Palo Alto, California, USA.

Journal of Periodontology
|April 13, 2020
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Summary

A new bone-cutting instrument yields more osteogenic autologous bone chips than conventional drills. Wnt signaling (WNT) therapy further enhances bone chip osteogenesis and peri-implant bone area around dental implants.

Keywords:
autograftgrafting, boneosteogenesisosteotomyregenerationwnt proteins

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Area of Science:

  • Regenerative Medicine
  • Biomaterials Science
  • Oral and Maxillofacial Surgery

Background:

  • Autologous bone chips are used in bone regeneration but their osteogenic potential varies with collection method.
  • Conventional drills and bone scrapers are common tools for harvesting bone, but may damage osteoprogenitor cells.
  • A novel slow-speed instrument for bone chip generation was developed to potentially improve osteogenesis.

Purpose of the Study:

  • To compare the osteogenic capacity of autologous bone chips generated by a new instrument versus conventional methods.
  • To investigate if Wnt signaling (WNT) therapy can enhance the osteogenic potential of these bone chips.
  • To evaluate the effect of WNT therapy on peri-implant bone regeneration in an immediate post-extraction implant model.

Main Methods:

  • Osteotomies were created in rat maxillary molar extraction sockets using a conventional drill or a new osseo-shaping instrument.
  • Titanium alloy implants were placed immediately after osteotomy preparation.
  • Bone chips were analyzed for cell viability and osteogenic potential using molecular, cellular, and histological methods; some were treated with a WNT therapeutic.

Main Results:

  • Bone chips from the new instrument exhibited preserved osteoprogenitor cell viability, unlike those from conventional drills which showed significant apoptosis.
  • Exogenous WNT therapeutic treatment increased the rate of osteogenesis around immediate post-extraction implants.
  • Sites treated with liposomal WNT3A (L-WNT3A) showed a significantly greater area of peri-implant bone compared to placebo controls.

Conclusions:

  • The new bone-cutting instrument produces more viable and osteogenic autologous bone chips compared to conventional drills.
  • Wnt signaling (WNT) therapy significantly enhances the osteogenic capacity of bone chips and promotes peri-implant bone regeneration.
  • This approach holds promise for improving outcomes in dental implant procedures requiring bone augmentation.