Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/34172
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dc.contributor.authorKoneski, F.en_US
dc.contributor.authorMonevska, D. Popoviken_US
dc.contributor.authorPopovski, V.en_US
dc.contributor.authorKirkov, A.en_US
dc.contributor.authorDvojakovska, S. Bozovicen_US
dc.contributor.authorPanchevski, G.en_US
dc.contributor.authorGrchev, A.en_US
dc.contributor.authorIliev, A.en_US
dc.contributor.authorIdoska, S.en_US
dc.contributor.authorStamatoski, A.en_US
dc.date.accessioned2025-10-20T09:33:31Z-
dc.date.available2025-10-20T09:33:31Z-
dc.date.issued2024-01-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/34172-
dc.description.abstractBackground: 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.isoenen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofInternational Journal of Oral and Maxillofacial Surgeryen_US
dc.subjectatorvastatin, medication-related ostenecrosis of the jawen_US
dc.titleATORVASTATIN PREVENTS MEDICATION-RELATED OSTEONECROSIS OF THE JAW IN RATSen_US
dc.typeArticleen_US
dc.relation.conferenceInternational conference on oral and maxillofacial surgery in Vancouver, Canadaen_US
dc.identifier.doi10.1016/j.ijom.2023.10.147-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S0901502723004368?httpAccept=text/xml-
dc.identifier.urlhttps://api.elsevier.com/content/article/PII:S0901502723004368?httpAccept=text/plain-
dc.identifier.volume52-
item.fulltextNo Fulltext-
item.grantfulltextnone-
Appears in Collections:Faculty of Dentistry: Articles
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