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Machine Learning Approaches for Predicting Bisphosphonate-Related Osteonecrosis in Women with Osteoporosis Using VEGFA Gene Polymorphisms

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dc.contributor.authorKim, Jin-Woo-
dc.contributor.authorYee, Jeong-
dc.contributor.authorOh, Sang-Hyeon-
dc.contributor.authorKim, Sun-Hyun-
dc.contributor.authorKim, Sun-Jong-
dc.contributor.authorChung, Jee-Eun-
dc.contributor.authorGwak, Hye-Sun-
dc.date.accessioned2021-07-28T08:08:20Z-
dc.date.available2021-07-28T08:08:20Z-
dc.date.created2021-07-22-
dc.date.issued2021-06-
dc.identifier.issn2075-4426-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/105737-
dc.description.abstractObjective: This nested case-control study aimed to investigate the effects of VEGFA polymorphisms on the development of bisphosphonate-related osteonecrosis of the jaw (BRONJ) in women with osteoporosis. Methods: Eleven single nucleotide polymorphisms (SNPs) of the VEGFA were assessed in a total of 125 patients. Logistic regression was performed for multivariable analysis. Machine learning algorithms, namely, fivefold cross-validated multivariate logistic regression, elastic net, random forest, and support vector machine, were developed to predict risk factors for BRONJ occurrence. Area under the receiver-operating curve (AUROC) analysis was conducted to assess clinical performance. Results: The VEGFA rs881858 was significantly associated with BRONJ development. The odds of BRONJ development were 6.45 times (95% CI, 1.69-24.65) higher among carriers of the wild-type rs881858 allele compared with variant homozygote carriers after adjusting for covariates. Additionally, variant homozygote (GG) carriers of rs10434 had higher odds than those with wild-type allele (OR, 3.16). Age >= 65 years (OR, 16.05) and bisphosphonate exposure >= 36 months (OR, 3.67) were also significant risk factors for BRONJ occurrence. AUROC values were higher than 0.78 for all machine learning methods employed in this study. Conclusion: Our study showed that the BRONJ occurrence was associated with VEGFA polymorphisms in osteoporotic women.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.titleMachine Learning Approaches for Predicting Bisphosphonate-Related Osteonecrosis in Women with Osteoporosis Using VEGFA Gene Polymorphisms-
dc.typeArticle-
dc.contributor.affiliatedAuthorChung, Jee-Eun-
dc.identifier.doi10.3390/jpm11060541-
dc.identifier.scopusid2-s2.0-85108696872-
dc.identifier.wosid000666063600001-
dc.identifier.bibliographicCitationJOURNAL OF PERSONALIZED MEDICINE, v.11, no.6, pp.1 - 10-
dc.relation.isPartOfJOURNAL OF PERSONALIZED MEDICINE-
dc.citation.titleJOURNAL OF PERSONALIZED MEDICINE-
dc.citation.volume11-
dc.citation.number6-
dc.citation.startPage1-
dc.citation.endPage10-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaHealth Care Sciences & Services-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
dc.relation.journalWebOfScienceCategoryHealth Care Sciences & Services-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.subject.keywordPlusENDOTHELIAL-GROWTH-FACTOR-
dc.subject.keywordPlusMEDICATION-RELATED OSTEONECROSIS-
dc.subject.keywordPlusMULTIPLE-MYELOMA-
dc.subject.keywordPlusRISK-FACTORS-
dc.subject.keywordPlusJAW-
dc.subject.keywordPlusPHARMACOGENETICS-
dc.subject.keywordPlusPREECLAMPSIA-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordAuthorbisphosphonate-related osteonecrosis-
dc.subject.keywordAuthorVEGFA-
dc.subject.keywordAuthorgene polymorphism-
dc.subject.keywordAuthormachine learning-
dc.identifier.urlhttps://www.mdpi.com/2075-4426/11/6/541-
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