Healing sequelae following tooth extraction and dental implant placement in an aged, ovariectomy model

• Published in: JBMR plus 2024-10, Vol.8 (10), p.ziae113
• Main Authors: Latimer, Jessica M, Maekawa, Shogo, Shiba, Takahiko, Fretwurst, Tobias, Chen, Michael, Larsson, Lena, Sugai, James V, Kostenuik, Paul, Mitlak, Bruce, Lanske, Beate, Giannobile, William V
• Format: Article
• Language: English
• Subjects: aging; bone regeneration; Endocrinology and Diabetes; Endokrinologi och diabetes; implant; osteoporosis; tooth extraction
• ISSN: 2473-4039; 2473-4039
• DOI: 10.1093/jbmrpl/ziae113

At present, a lack of consensus exists regarding the clinical impact of osteoporosis on alveolar bone metabolism during implant osseointegration. While limited preclinical and clinical evidence demonstrates a negative influence of osteoporosis on dental extraction socket healing, no preclinical studies offer data on the results of implant placement in 6-mo-old, ovariectomized (OVX) Sprague-Dawley rats. This study aimed to investigate the outcomes of dental tooth extraction socket healing and implant placement in a rodent model of osteoporosis following daily vehicle (VEH) or abaloparatide (ABL) administration. Micro-CT and histologic analysis demonstrated signs of delayed wound healing, consistent with alveolar osteitis in extraction sockets following 42 d of healing in both the VEH and ABL groups. In a semiquantitative histological analysis, the OVX-ABL group demonstrated a tendency for improved socket regeneration with a 3-fold greater rate for moderate socket healing when compared to the OVX-VEH group (43% vs 14%), however, this finding was not statistically significant ( =.11). No significant differences were observed between vehicle and test groups in terms of implant outcomes (BMD and bone volume/total volume) at 14- and 21-d post-implant placement. Abaloparatide (ABL) significantly increased BMD of the femoral shaft and intact maxillary alveolar bone sites in OVX animals, demonstrating the therapeutic potential for oral hard tissue regeneration. The present model involving estrogen-deficiency-induced bone loss demonstrated an impaired healing response to dental extraction and implant installation.