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Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men

The study aimed to utilize machine learning (ML) approaches and genomic data to develop a prediction model for bone mineral density (BMD) and identify the best modeling approach for BMD prediction. The genomic and phenotypic data of Osteoporotic Fractures in Men Study (n = 5130) was analyzed. Geneti...

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Autores principales: Wu, Qing, Nasoz, Fatma, Jung, Jongyun, Bhattarai, Bibek, Han, Mira V., Greenes, Robert A., Saag, Kenneth G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904941/
https://www.ncbi.nlm.nih.gov/pubmed/33627720
http://dx.doi.org/10.1038/s41598-021-83828-3
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author Wu, Qing
Nasoz, Fatma
Jung, Jongyun
Bhattarai, Bibek
Han, Mira V.
Greenes, Robert A.
Saag, Kenneth G.
author_facet Wu, Qing
Nasoz, Fatma
Jung, Jongyun
Bhattarai, Bibek
Han, Mira V.
Greenes, Robert A.
Saag, Kenneth G.
author_sort Wu, Qing
collection PubMed
description The study aimed to utilize machine learning (ML) approaches and genomic data to develop a prediction model for bone mineral density (BMD) and identify the best modeling approach for BMD prediction. The genomic and phenotypic data of Osteoporotic Fractures in Men Study (n = 5130) was analyzed. Genetic risk score (GRS) was calculated from 1103 associated SNPs for each participant after a comprehensive genotype imputation. Data were normalized and divided into a training set (80%) and a validation set (20%) for analysis. Random forest, gradient boosting, neural network, and linear regression were used to develop BMD prediction models separately. Ten-fold cross-validation was used for hyper-parameters optimization. Mean square error and mean absolute error were used to assess model performance. When using GRS and phenotypic covariates as the predictors, all ML models’ performance and linear regression in BMD prediction were similar. However, when replacing GRS with the 1103 individual SNPs in the model, ML models performed significantly better than linear regression (with lasso regularization), and the gradient boosting model performed the best. Our study suggested that ML models, especially gradient boosting, can improve BMD prediction in genomic data.
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spelling pubmed-79049412021-02-26 Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men Wu, Qing Nasoz, Fatma Jung, Jongyun Bhattarai, Bibek Han, Mira V. Greenes, Robert A. Saag, Kenneth G. Sci Rep Article The study aimed to utilize machine learning (ML) approaches and genomic data to develop a prediction model for bone mineral density (BMD) and identify the best modeling approach for BMD prediction. The genomic and phenotypic data of Osteoporotic Fractures in Men Study (n = 5130) was analyzed. Genetic risk score (GRS) was calculated from 1103 associated SNPs for each participant after a comprehensive genotype imputation. Data were normalized and divided into a training set (80%) and a validation set (20%) for analysis. Random forest, gradient boosting, neural network, and linear regression were used to develop BMD prediction models separately. Ten-fold cross-validation was used for hyper-parameters optimization. Mean square error and mean absolute error were used to assess model performance. When using GRS and phenotypic covariates as the predictors, all ML models’ performance and linear regression in BMD prediction were similar. However, when replacing GRS with the 1103 individual SNPs in the model, ML models performed significantly better than linear regression (with lasso regularization), and the gradient boosting model performed the best. Our study suggested that ML models, especially gradient boosting, can improve BMD prediction in genomic data. Nature Publishing Group UK 2021-02-24 /pmc/articles/PMC7904941/ /pubmed/33627720 http://dx.doi.org/10.1038/s41598-021-83828-3 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wu, Qing
Nasoz, Fatma
Jung, Jongyun
Bhattarai, Bibek
Han, Mira V.
Greenes, Robert A.
Saag, Kenneth G.
Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title_full Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title_fullStr Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title_full_unstemmed Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title_short Machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
title_sort machine learning approaches for the prediction of bone mineral density by using genomic and phenotypic data of 5130 older men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904941/
https://www.ncbi.nlm.nih.gov/pubmed/33627720
http://dx.doi.org/10.1038/s41598-021-83828-3
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