The Role of Apical Periodontitis Disease in the Development of Bisphosphonate-Related Osteonecrosis of the Jaw: An Animal Study

Author:

Marques-Ferreira Manuel1234ORCID,Abrantes Ana Margarida1345ORCID,Paula Anabela1346ORCID,Laranjo Mafalda1345ORCID,Pires Ana Salomé1345ORCID,Caramelo Francisco134ORCID,Segura-Egea Juan José7ORCID,Brito Ana1,Carvalho Lina148,Botelho Maria Filomena1345ORCID,Carrilho Eunice136ORCID,Marto Carlos Miguel13469ORCID,Paulo Siri124ORCID

Affiliation:

1. Univ. Coimbra, Coimbra Institute for Clinical and Biomedical Research (iCBR), Area of Environment, Genetics and Oncobiology (CIMAGO), Faculty of Medicine, 3000-548 Coimbra, Portugal

2. Univ. Coimbra, Institute of Endodontics, Faculty of Medicine, 3000-548 Coimbra, Portugal

3. Univ. Coimbra, Center for Innovative Biomedicine and Biotechnology (CIBB), 3004-504 Coimbra, Portugal

4. Clinical Academic Center of Coimbra (CACC), 3004-561 Coimbra, Portugal

5. Univ. Coimbra, Institute of Biophysics, Faculty of Medicine, 3000-548 Coimbra, Portugal

6. Univ. Coimbra, Institute of Integrated Clinical Practice and Laboratory for Evidence-Based Sciences and Precision Dentistry (LACBE–MDP), Faculty of Medicine, 3000-548 Coimbra, Portugal

7. Department of Stomatology (Endodontics Section), University of Sevilla, 41009 Sevilla, Spain

8. Univ. of Coimbra, IAP, Faculty of Medicine, 3004-504 Coimbra, Portugal

9. Univ. of Coimbra, Institute of Experimental Pathology, Faculty of Medicine, 3000-548 Coimbra, Portugal

Abstract

Background: Microorganisms and their by-products are responsible for establishing pulpal and periapical diseases. Healing is compromised in patients under bisphosphonate therapy, and the presence of periapical infections can potentially lead to the development of medication-related osteonecrosis of the jaw (MRONJ). This work aimed to evaluate if bisphosphonate therapy is a risk factor for MRONJ development in the presence of periapical lesions. Methods: Two groups of 10 female Wistar rats were used. The experimental group received zoledronate (0.1 mg/kg) intraperitoneally, and the control received a saline solution, three times a week for three weeks. One week after the last injection, apical periodontitis was induced through pulpal exposure in the mandibular first molars. Twenty-one days later, the animals were intravenously injected with 99mTc-HMDP, and the radioactivity uptake by mandibular specimens was counted. In addition, sample radiographs and a histological examination were performed. Results: The bone loss was higher in the control group when compared to the experimental group (p = 0.027). 99mTc-HMDP uptake in the control was reduced compared with the experimental group, although without statistical significance. Conclusions: In the presence of zoledronate therapy, apical periodontitis does not increase the risk of MRONJ development, and periapical lesions have lower bone resorption when compared to the control group.

Funder

Foundation for Science and Technology (FCT), Portugal

Publisher

MDPI AG

Subject

General Dentistry

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