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Biomarkers to predict the onset of biphosphonate-related osteonecrosis of the jaw: A systematic review

Lorenzo Pouso, Alejandro Ismael; Pérez Sayáns, Mario; Gonzalez-Palanca, S.; Chamorro Petronacci, Cintia Micaela; Bagan, J.; García García, Abel
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URI: http://hdl.handle.net/20.500.11940/15672
PMID: 30595601
DOI: 10.4317/medoral.22763
ISSN: 1698-4447
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Med Oral Patol Oral Cir Bucal. 2019 Jan 1;24(1):e26-e36. (957.7Kb)
Fecha de publicación
2019
Título de revista
Medicina Oral, Patologia Oral y Cirugia Bucal
Tipo de contenido
Artigo
DeCS
estudios de casos y controles | pruebas de valores predictivos | osteonecrosis mandíbular asociada a bifosfonatos | evaluación de riesgos | humanos
MeSH
Predictive Value of Tests | Risk Assessment | Humans | Bisphosphonate-Associated Osteonecrosis of the Jaw | Case-Control Studies
Resumen
BACKGROUND: The goal of this paper was to identify available biomarkers to predict the onset of biphosphonate-related osteonecrosis of the jaw (BRONJ). MATERIAL AND METHODS: Case-control studies comparing the different concentrations of a series of molecules detected in serum and urine as matrices of BRONJ affected patients vs. non-affected were included. PRISMA guidelines for systematic reviews were used for the present paper. Two reviewers independently screened electronic databases (Medline, Web of science, and The Cochrane Library) and performed hand searches. Risk of bias assessment of selected studies was performed by the Newcastle-Ottawa Scale. This study is registered as PROSPERO CRD42017078149. RESULTS: From a total of 601 identified studies, 7 (4 articles with high methodological quality and 3 with medium) articles were included. They investigate 2623 patients, of whom 91 (3.47%) developed BRONJ. A total of 7 biomarkers were identified and classified into 3 groups: bone turnover, angiogenesis and endocrine markers. Conflicting results were found in relation to most biomarkers. CONCLUSIONS: The present review suggests that no useful markers are currently available to evaluate BRONJ risk. Nevertheless, the present paper indicates that a paradigm shift from bone turnover biomarkers to angiogenesis and endocrine markers could shed light on this search.

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