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Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw
OBJECTIVES: The objective of this study was to retrospectively investigate the association of diseases having an influence on inhibition of angiogenesis such as hypertension, diabetes mellitus type II, hypercholesterolemia, and rheumatoid arthritis (RA) with the development of osteonecrosis of the j...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Association of Oral and Maxillofacial Surgeons
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104869/ https://www.ncbi.nlm.nih.gov/pubmed/27847735 http://dx.doi.org/10.5125/jkaoms.2016.42.5.271 |
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author | Paek, Seung Jae Park, Won-Jong Shin, Ho-Sung Choi, Moon-Gi Kwon, Kyung-Hwan Choi, Eun Joo |
author_facet | Paek, Seung Jae Park, Won-Jong Shin, Ho-Sung Choi, Moon-Gi Kwon, Kyung-Hwan Choi, Eun Joo |
author_sort | Paek, Seung Jae |
collection | PubMed |
description | OBJECTIVES: The objective of this study was to retrospectively investigate the association of diseases having an influence on inhibition of angiogenesis such as hypertension, diabetes mellitus type II, hypercholesterolemia, and rheumatoid arthritis (RA) with the development of osteonecrosis of the jaws. MATERIALS AND METHODS: The 135 patients were allocated into 4 groups of bisphosphonate-related osteonecrosis of the jaw (BRONJ) group (1A); non-BRONJ group (1B); osteonecrosis of the jaw (ONJ) group (2A); and control group (2B), according to histologic results and use of bisphosphonate. This retrospective study was conducted with patients who were treated in one institute from 2012 to 2013. Fisher's exact test and logistic regression analysis were used to analyze the odds ratios of diseases having an influence on inhibition of angiogenesis for development of ONJ. RESULTS: The effects of diabetes and hypertension were not statistically significant on development of ONJ. When not considering bisphosphonate use, RA exhibited a high odds ratio of 3.23 (P=0.094), while hyperlipidemia showed an odds ratio of 2.10 (P=0.144) for development of ONJ. More than one disease that had an influence on inhibition of angiogenesis showed a statistically significant odds ratio of 2.54 (P=0.012) for development of ONJ. CONCLUSION: Patients without diseases having an influence on inhibition of angiogenesis were at less risk for developing ONJ. |
format | Online Article Text |
id | pubmed-5104869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Association of Oral and Maxillofacial Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-51048692016-11-15 Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw Paek, Seung Jae Park, Won-Jong Shin, Ho-Sung Choi, Moon-Gi Kwon, Kyung-Hwan Choi, Eun Joo J Korean Assoc Oral Maxillofac Surg Original Article OBJECTIVES: The objective of this study was to retrospectively investigate the association of diseases having an influence on inhibition of angiogenesis such as hypertension, diabetes mellitus type II, hypercholesterolemia, and rheumatoid arthritis (RA) with the development of osteonecrosis of the jaws. MATERIALS AND METHODS: The 135 patients were allocated into 4 groups of bisphosphonate-related osteonecrosis of the jaw (BRONJ) group (1A); non-BRONJ group (1B); osteonecrosis of the jaw (ONJ) group (2A); and control group (2B), according to histologic results and use of bisphosphonate. This retrospective study was conducted with patients who were treated in one institute from 2012 to 2013. Fisher's exact test and logistic regression analysis were used to analyze the odds ratios of diseases having an influence on inhibition of angiogenesis for development of ONJ. RESULTS: The effects of diabetes and hypertension were not statistically significant on development of ONJ. When not considering bisphosphonate use, RA exhibited a high odds ratio of 3.23 (P=0.094), while hyperlipidemia showed an odds ratio of 2.10 (P=0.144) for development of ONJ. More than one disease that had an influence on inhibition of angiogenesis showed a statistically significant odds ratio of 2.54 (P=0.012) for development of ONJ. CONCLUSION: Patients without diseases having an influence on inhibition of angiogenesis were at less risk for developing ONJ. The Korean Association of Oral and Maxillofacial Surgeons 2016-10 2016-10-25 /pmc/articles/PMC5104869/ /pubmed/27847735 http://dx.doi.org/10.5125/jkaoms.2016.42.5.271 Text en Copyright © 2016 The Korean Association of Oral and Maxillofacial Surgeons. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Paek, Seung Jae Park, Won-Jong Shin, Ho-Sung Choi, Moon-Gi Kwon, Kyung-Hwan Choi, Eun Joo Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title | Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title_full | Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title_fullStr | Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title_full_unstemmed | Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title_short | Diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
title_sort | diseases having an influence on inhibition of angiogenesis as risk factors of osteonecrosis of the jaw |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104869/ https://www.ncbi.nlm.nih.gov/pubmed/27847735 http://dx.doi.org/10.5125/jkaoms.2016.42.5.271 |
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