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

Authors
Kim, Jin-WooYee, JeongOh, Sang-HyeonKim, Sun-HyunKim, Sun-JongChung, Jee-EunGwak, Hye-Sun
Issue Date
Jun-2021
Publisher
MDPI
Keywords
bisphosphonate-related osteonecrosis; VEGFA; gene polymorphism; machine learning
Citation
JOURNAL OF PERSONALIZED MEDICINE, v.11, no.6, pp.1 - 10
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PERSONALIZED MEDICINE
Volume
11
Number
6
Start Page
1
End Page
10
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/105737
DOI
10.3390/jpm11060541
ISSN
2075-4426
Abstract
Objective: 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.
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