Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/34172
DC Field | Value | Language |
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dc.contributor.author | Koneski, F. | en_US |
dc.contributor.author | Monevska, D. Popovik | en_US |
dc.contributor.author | Popovski, V. | en_US |
dc.contributor.author | Kirkov, A. | en_US |
dc.contributor.author | Dvojakovska, S. Bozovic | en_US |
dc.contributor.author | Panchevski, G. | en_US |
dc.contributor.author | Grchev, A. | en_US |
dc.contributor.author | Iliev, A. | en_US |
dc.contributor.author | Idoska, S. | en_US |
dc.contributor.author | Stamatoski, A. | en_US |
dc.date.accessioned | 2025-10-20T09:33:31Z | - |
dc.date.available | 2025-10-20T09:33:31Z | - |
dc.date.issued | 2024-01 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.12188/34172 | - |
dc.description.abstract | Background: Medication-related osteonecrosis of the jaw (MRONJ) is a serious complication of antiresorptive drugs, that is still a subject of clinical and experimental research. Recent studies show that statins might have a potential positive effect on bone metabolism via stimu- lation of osteoblastic activity. Aim: The aim of this study is to assess the effects of atorvastatin on the prevention of MRONJ. Methods: Twenty-five white laboratory Wistar rats were divided equally in five groups. Positive control group received only saline i.p. while all other groups received 0.06 mg/kg zoledronic acid i.p., once weekly for seven weeks, including the negative control group. In addition, examined groups 1, 2 and 3 received a single atorvastatin injection on the extraction site immediately after the extraction, once weekly intraperitoneal atorvastatin in- jection for seven weeks, and local injection of atorva- statin two weeks after the tooth extraction, respectively. Tooth extraction was performed in all groups on day 21. Clinical scores of wound healing and three-dimensional cone-beam computed tomography (CBCT) were per- formed to evaluate the occurrence of MRONJ. Mann- Whitney U test was used for statistical analysis and P value of <0.05 was considered as significant. Results: Negative control group showed significantly impaired wound healing, with exposed necrotic bone, confirmed with osteolytic lesions on CBCT. All groups treated with atorvastatin showed statistically sig- nificant improved wound healing, less osteonecrosis and better scores on CBCT evaluation, when com- pared to negative control group, but similar to posi- tive control group. Conclusion: Atorvastatin may be an option for preven- tion and treatment of MRONJ. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier BV | en_US |
dc.relation.ispartof | International Journal of Oral and Maxillofacial Surgery | en_US |
dc.subject | atorvastatin, medication-related ostenecrosis of the jaw | en_US |
dc.title | ATORVASTATIN PREVENTS MEDICATION-RELATED OSTEONECROSIS OF THE JAW IN RATS | en_US |
dc.type | Article | en_US |
dc.relation.conference | International conference on oral and maxillofacial surgery in Vancouver, Canada | en_US |
dc.identifier.doi | 10.1016/j.ijom.2023.10.147 | - |
dc.identifier.url | https://api.elsevier.com/content/article/PII:S0901502723004368?httpAccept=text/xml | - |
dc.identifier.url | https://api.elsevier.com/content/article/PII:S0901502723004368?httpAccept=text/plain | - |
dc.identifier.volume | 52 | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | Faculty of Dentistry: Articles |
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