Modelling future bone mineral density: Simplicity or complexity?
Osteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in...
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Published in | Bone (New York, N.Y.) Vol. 187; p. 117178 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.10.2024
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ISSN | 8756-3282 1873-2763 1873-2763 |
DOI | 10.1016/j.bone.2024.117178 |
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Abstract | Osteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in BMD over time contribute to fracture risk. Predicting future fracture in individual patients is challenging and impacts clinical decisions such as when to intervene or repeat BMD measurement. Although the importance of BMD change is recognised, an effective way to incorporate this marginal effect into clinical algorithms is lacking.
We compared two methods using longitudinal DXA data generated from subjects with two or more hip DXA scans on the same machine between 2000 and 2018. A simpler statistical method (ZBM) was used to predict an individual's future BMD based on the mean BMD and the standard deviation of the reference group and their BMD measured in the latest scan. A more complex deep learning (DL)-based method was developed to cope with multidimensional longitudinal data, variables extracted from patients' historical DXA scan(s), as well as features drawn from the ZBM method. Sensitivity analyses of several subgroups was conducted to evaluate the performance of the derived models.
2948 white adults aged 40–90 years met our study inclusion: 2652 (90 %) females and 296 (10 %) males. Our DL-based models performed significantly better than the ZBM models in women, particularly our Hybrid-DL model. In contrast, the ZBM-based models performed as well or better than DL-based models in men.
Deep learning-based and statistical models have potential to forecast future BMD using longitudinal clinical data. These methods have the potential to augment clinical decisions regarding when to repeat BMD testing in the assessment of osteoporosis.
•Statistical techniques & DL-based techniques can be used to develop models to predict future BMD.•The DL-based models performed better in women than men.•The ZBM-based models performed as well/better than the DL-based models in men.•These models can augment clinical decisions regarding when to repeat BMD testing. |
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AbstractList | Osteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in BMD over time contribute to fracture risk. Predicting future fracture in individual patients is challenging and impacts clinical decisions such as when to intervene or repeat BMD measurement. Although the importance of BMD change is recognised, an effective way to incorporate this marginal effect into clinical algorithms is lacking.BACKGROUNDOsteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in BMD over time contribute to fracture risk. Predicting future fracture in individual patients is challenging and impacts clinical decisions such as when to intervene or repeat BMD measurement. Although the importance of BMD change is recognised, an effective way to incorporate this marginal effect into clinical algorithms is lacking.We compared two methods using longitudinal DXA data generated from subjects with two or more hip DXA scans on the same machine between 2000 and 2018. A simpler statistical method (ZBM) was used to predict an individual's future BMD based on the mean BMD and the standard deviation of the reference group and their BMD measured in the latest scan. A more complex deep learning (DL)-based method was developed to cope with multidimensional longitudinal data, variables extracted from patients' historical DXA scan(s), as well as features drawn from the ZBM method. Sensitivity analyses of several subgroups was conducted to evaluate the performance of the derived models.METHODSWe compared two methods using longitudinal DXA data generated from subjects with two or more hip DXA scans on the same machine between 2000 and 2018. A simpler statistical method (ZBM) was used to predict an individual's future BMD based on the mean BMD and the standard deviation of the reference group and their BMD measured in the latest scan. A more complex deep learning (DL)-based method was developed to cope with multidimensional longitudinal data, variables extracted from patients' historical DXA scan(s), as well as features drawn from the ZBM method. Sensitivity analyses of several subgroups was conducted to evaluate the performance of the derived models.2948 white adults aged 40-90 years met our study inclusion: 2652 (90 %) females and 296 (10 %) males. Our DL-based models performed significantly better than the ZBM models in women, particularly our Hybrid-DL model. In contrast, the ZBM-based models performed as well or better than DL-based models in men.RESULTS2948 white adults aged 40-90 years met our study inclusion: 2652 (90 %) females and 296 (10 %) males. Our DL-based models performed significantly better than the ZBM models in women, particularly our Hybrid-DL model. In contrast, the ZBM-based models performed as well or better than DL-based models in men.Deep learning-based and statistical models have potential to forecast future BMD using longitudinal clinical data. These methods have the potential to augment clinical decisions regarding when to repeat BMD testing in the assessment of osteoporosis.CONCLUSIONSDeep learning-based and statistical models have potential to forecast future BMD using longitudinal clinical data. These methods have the potential to augment clinical decisions regarding when to repeat BMD testing in the assessment of osteoporosis. Osteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in BMD over time contribute to fracture risk. Predicting future fracture in individual patients is challenging and impacts clinical decisions such as when to intervene or repeat BMD measurement. Although the importance of BMD change is recognised, an effective way to incorporate this marginal effect into clinical algorithms is lacking. We compared two methods using longitudinal DXA data generated from subjects with two or more hip DXA scans on the same machine between 2000 and 2018. A simpler statistical method (ZBM) was used to predict an individual's future BMD based on the mean BMD and the standard deviation of the reference group and their BMD measured in the latest scan. A more complex deep learning (DL)-based method was developed to cope with multidimensional longitudinal data, variables extracted from patients' historical DXA scan(s), as well as features drawn from the ZBM method. Sensitivity analyses of several subgroups was conducted to evaluate the performance of the derived models. 2948 white adults aged 40–90 years met our study inclusion: 2652 (90 %) females and 296 (10 %) males. Our DL-based models performed significantly better than the ZBM models in women, particularly our Hybrid-DL model. In contrast, the ZBM-based models performed as well or better than DL-based models in men. Deep learning-based and statistical models have potential to forecast future BMD using longitudinal clinical data. These methods have the potential to augment clinical decisions regarding when to repeat BMD testing in the assessment of osteoporosis. •Statistical techniques & DL-based techniques can be used to develop models to predict future BMD.•The DL-based models performed better in women than men.•The ZBM-based models performed as well/better than the DL-based models in men.•These models can augment clinical decisions regarding when to repeat BMD testing. Osteoporotic fractures are a major global public health issue, leading to patient suffering and death, and considerable healthcare costs. Bone mineral density (BMD) measurement is important to identify those with osteoporosis and assess their risk of fracture. Both the absolute BMD and the change in BMD over time contribute to fracture risk. Predicting future fracture in individual patients is challenging and impacts clinical decisions such as when to intervene or repeat BMD measurement. Although the importance of BMD change is recognised, an effective way to incorporate this marginal effect into clinical algorithms is lacking. We compared two methods using longitudinal DXA data generated from subjects with two or more hip DXA scans on the same machine between 2000 and 2018. A simpler statistical method (ZBM) was used to predict an individual's future BMD based on the mean BMD and the standard deviation of the reference group and their BMD measured in the latest scan. A more complex deep learning (DL)-based method was developed to cope with multidimensional longitudinal data, variables extracted from patients' historical DXA scan(s), as well as features drawn from the ZBM method. Sensitivity analyses of several subgroups was conducted to evaluate the performance of the derived models. 2948 white adults aged 40-90 years met our study inclusion: 2652 (90 %) females and 296 (10 %) males. Our DL-based models performed significantly better than the ZBM models in women, particularly our Hybrid-DL model. In contrast, the ZBM-based models performed as well or better than DL-based models in men. Deep learning-based and statistical models have potential to forecast future BMD using longitudinal clinical data. These methods have the potential to augment clinical decisions regarding when to repeat BMD testing in the assessment of osteoporosis. |
ArticleNumber | 117178 |
Author | Whelan, Bryan Rooney, Bridie Silke, Carmel Wang, Tingyan McPartland, Aoife Brennan, Attracta O'Malley, Gráinne Yang, Lan Ebrahimiarjestan, Mina Erjiang, E. Chan, Wing P. Carey, John J. O'Sullivan, Miriam Dempsey, Mary Yu, Ming |
Author_xml | – sequence: 1 givenname: E. surname: Erjiang fullname: Erjiang, E. organization: School of Management, Guangxi Minzu Univeristy, Nanning, China – sequence: 2 givenname: John J. surname: Carey fullname: Carey, John J. organization: School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Ireland – sequence: 3 givenname: Tingyan surname: Wang fullname: Wang, Tingyan organization: Nuffield Department of Medicine, University of Oxford, Oxford, UK – sequence: 4 givenname: Mina surname: Ebrahimiarjestan fullname: Ebrahimiarjestan, Mina organization: Department of Industrial Engineering, Tsinghua University, Beijing, China – sequence: 5 givenname: Lan surname: Yang fullname: Yang, Lan organization: Insight SFI Research Centre for Data Analytics, Data Science Institute, University of Galway, Ireland – sequence: 6 givenname: Mary surname: Dempsey fullname: Dempsey, Mary organization: School of Engineering, College of Science and Engineering, University of Galway, Ireland – sequence: 7 givenname: Ming surname: Yu fullname: Yu, Ming organization: Department of Industrial Engineering, Tsinghua University, Beijing, China – sequence: 8 givenname: Wing P. surname: Chan fullname: Chan, Wing P. organization: Department of Radiology, Wan Fang Hospital, Taipei Medical University, Taiwan – sequence: 9 givenname: Bryan surname: Whelan fullname: Whelan, Bryan organization: School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Ireland – sequence: 10 givenname: Carmel surname: Silke fullname: Silke, Carmel organization: School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Ireland – sequence: 11 givenname: Miriam surname: O'Sullivan fullname: O'Sullivan, Miriam organization: School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Ireland – sequence: 12 givenname: Bridie surname: Rooney fullname: Rooney, Bridie organization: Department of Geriatric Medicine, Sligo University Hospital, Sligo, Ireland – sequence: 13 givenname: Aoife surname: McPartland fullname: McPartland, Aoife organization: Department of Rheumatology, Our Lady's Hospital, Manorhamilton, Co. Leitrim, Ireland – sequence: 14 givenname: Gráinne surname: O'Malley fullname: O'Malley, Gráinne organization: School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Ireland – sequence: 15 givenname: Attracta surname: Brennan fullname: Brennan, Attracta email: attracta.brennan@universityofgalway.ie organization: School of Computer Science, College of Science and Engineering, University of Galway, Ireland |
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Keywords | Deep learning Longitudinal monitoring Z-score Osteoporosis Bone mineral density Decision making |
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