Volume 21, Issue 1 pp. 4-10
CASE REPORT

Clinical application of autogenous demineralized dentin matrix loaded with recombinant human bone morphogenetic-2 for socket preservation: A case series

In-Woong Um PhD, DDS

Corresponding Author

In-Woong Um PhD, DDS

R&D Institute, Korea Tooth Bank, Seoul, Republic of Korea

Correspondence

In-Woong Um, R&D Institute, Korea Tooth Bank, 622 Eonju-ro, Gangnam-gu, Seoul 135-832, Republic of Korea.

Email: [email protected]

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Young-Kyun Kim PhD, DDS

Young-Kyun Kim PhD, DDS

Department of Oral and Maxillofacial Surgery, Section of Dentistry, Seoul National University Bundang Hospital, Seongnam, Republic of Korea

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Joo-Cheol Park PhD, DDS

Joo-Cheol Park PhD, DDS

Department of Oral Histology-Departmental Biology, School of Dentistry, Seoul National University, Seoul, Republic of Korea

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Jong-Ho Lee PhD, DDS

Jong-Ho Lee PhD, DDS

Clinical Trial Center, Seoul National University Dental Hospital, Seoul, South Korea

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First published: 27 December 2018
Citations: 27
Funding information Korea Health Industry Development Institute, Grant/Award Number: HI15C1535

Abstract

Background

Demineralized dentin matrix (DDM) has potential application as a carrier for recombinant human bone morphogenetic protein-2 (rhBMP-2) in bone regeneration.

Purpose

To evaluate the efficacy of DDM loaded with rhBMP-2 for socket preservation.

Materials and Methods

DDM loaded with rhBMP-2 (DDM/rhBMP-2) was applied to 10 experimental sites and DDM alone to 6 control sites. The changes in height and width of the extraction socket after preservation were measured by cone beam computed tomography. Trephine cores were harvested for histomorphometric evaluation before placement of the implant.

Results

The reductions in height and width of the socket were more significant in the group treated with DDM than in the group treated with DDM/rhBMP-2. The amount of new bone formation was 34.39% with DDM/rhBMP-2 and 29.75% with DDM; the respective amounts of residual dentin were 8.35% and 16.15%. Although the differences were not statistically significant, the dimensional changes, amount of bone formation, and replacement of DDM in DDM/rhBMP-2 with bone were superior to those of DDM alone.

Conclusions

Within the limitations of this study, we suggest that DDM may be a potential carrier for rhBMP-2 and that it may be possible to reduce the rhBMP-2 concentration to 0.2 mg/mL.

CONFLICT OF INTEREST

No conflicts of interest.

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