<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wu Q</submitter><funding>National Institute of Aging</funding><funding>NIA NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>National Institute on Minority Health and Health Disparities</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>462-472</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11262147</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>39(4)</volume><pubmed_abstract>This study aimed to enhance the fracture risk prediction accuracy in major osteoporotic fractures (MOFs) and hip fractures (HFs) by integrating genetic profiles, machine learning (ML) techniques, and Bayesian optimization. The genetic risk score (GRS), derived from 1,103 risk single nucleotide polymorphisms (SNPs) from genome-wide association studies (GWAS), was formulated for 25,772 postmenopausal women from the Women's Health Initiative dataset. We developed four ML models: Support Vector Machine (SVM), Random Forest, XGBoost, and Artificial Neural Network (ANN) for binary fracture outcome and 10-year fracture risk prediction. GRS and FRAX clinical risk factors (CRFs) were used as predictors. Death as a competing risk was accounted for in ML models for time-to-fracture data. ML models we</pubmed_abstract><journal>Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research</journal><pubmed_title>Enhanced osteoporotic fracture prediction in postmenopausal women using Bayesian optimization of machine learning models with genetic risk score.</pubmed_title><pmcid>PMC11262147</pmcid><funding_grant_id>R21 MD013681</funding_grant_id><funding_grant_id>R01 AG080017</funding_grant_id><funding_grant_id>R21MD013681</funding_grant_id><funding_grant_id>P20 GM121325</funding_grant_id><funding_grant_id>P20GM121325</funding_grant_id><funding_grant_id>R01AG080017</funding_grant_id><pubmed_authors>Wu Q</pubmed_authors><pubmed_authors>Dai J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Enhanced osteoporotic fracture prediction in postmenopausal women using Bayesian optimization of machine learning models with genetic risk score.</name><description>This study aimed to enhance the fracture risk prediction accuracy in major osteoporotic fractures (MOFs) and hip fractures (HFs) by integrating genetic profiles, machine learning (ML) techniques, and Bayesian optimization. The genetic risk score (GRS), derived from 1,103 risk single nucleotide polymorphisms (SNPs) from genome-wide association studies (GWAS), was formulated for 25,772 postmenopausal women from the Women's Health Initiative dataset. We developed four ML models: Support Vector Machine (SVM), Random Forest, XGBoost, and Artificial Neural Network (ANN) for binary fracture outcome and 10-year fracture risk prediction. GRS and FRAX clinical risk factors (CRFs) were used as predictors. Death as a competing risk was accounted for in ML models for time-to-fracture data. ML models we</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2025-04-05T11:34:25.563Z</modification><creation>2025-04-05T11:34:25.563Z</creation></dates><accession>S-EPMC11262147</accession><cross_references><pubmed>38477741</pubmed><doi>10.1093/jbmr/zjae025</doi></cross_references></HashMap>