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一种使用机器学习和不确定性量化来预测髋部骨折风险的分阶段方法。

A Staged Approach using Machine Learning and Uncertainty Quantification to Predict the Risk of Hip Fracture.

作者信息

Shaik Anjum, Larsen Kristoffer, Lane Nancy E, Zhao Chen, Su Kuan-Jui, Keyak Joyce H, Tian Qing, Sha Qiuying, Shen Hui, Deng Hong-Wen, Zhou Weihua

机构信息

Department of Applied Computing, Michigan Technological University, 1400 Townsend Dr, Houghton, MI, 49931.

Department of Mathematical Sciences, Michigan Technological University, Houghton, MI, USA.

出版信息

ArXiv. 2024 May 30:arXiv:2405.20071v1.

PMID:38855554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11160872/
Abstract

Hip fractures present a significant healthcare challenge, especially within aging populations, where they are often caused by falls. These fractures lead to substantial morbidity and mortality, emphasizing the need for timely surgical intervention. Despite advancements in medical care, hip fractures impose a significant burden on individuals and healthcare systems. This paper focuses on the prediction of hip fracture risk in older and middle-aged adults, where falls and compromised bone quality are predominant factors. We propose a novel staged model that combines advanced imaging and clinical data to improve predictive performance. By using convolutional neural networks (CNNs) to extract features from hip DXA images, along with clinical variables, shape measurements, and texture features, our method provides a comprehensive framework for assessing fracture risk. The study cohort included 547 patients, with 94 experiencing hip fracture. A staged machine learning-based model was developed using two ensemble models: Ensemble 1 (clinical variables only) and Ensemble 2 (clinical variables and DXA imaging features). This staged approach used uncertainty quantification from Ensemble 1 to decide if DXA features are necessary for further prediction. Ensemble 2 exhibited the highest performance, achieving an Area Under the Curve (AUC) of 0.9541, an accuracy of 0.9195, a sensitivity of 0.8078, and a specificity of 0.9427. The staged model also performed well, with an AUC of 0.8486, an accuracy of 0.8611, a sensitivity of 0.5578, and a specificity of 0.9249, outperforming Ensemble 1, which had an AUC of 0.5549, an accuracy of 0.7239, a sensitivity of 0.1956, and a specificity of 0.8343. Furthermore, the staged model suggested that 54.49% of patients did not require DXA scanning. It effectively balanced accuracy and specificity, offering a robust solution when DXA data acquisition is not always feasible. Statistical tests confirmed significant differences between the models, highlighting the advantages of the advanced modeling strategies. Our staged approach offers a cost-effective holistic view of patients' health. It could identify individuals at risk with a high accuracy but reduce the unnecessary DXA scanning. Our approach has great promise to guide interventions to prevent hip fractures with reduced cost and radiation.

摘要

髋部骨折对医疗保健构成了重大挑战,尤其是在老年人群中,髋部骨折通常由跌倒引起。这些骨折会导致严重的发病率和死亡率,凸显了及时进行手术干预的必要性。尽管医疗有所进步,但髋部骨折给个人和医疗系统带来了沉重负担。本文聚焦于预测中老年成年人的髋部骨折风险,其中跌倒和骨质受损是主要因素。我们提出了一种新颖的分阶段模型,该模型结合了先进的影像学和临床数据以提高预测性能。通过使用卷积神经网络(CNN)从髋部双能X线吸收测定(DXA)图像中提取特征,并结合临床变量、形态测量和纹理特征,我们的方法为评估骨折风险提供了一个全面的框架。研究队列包括547名患者,其中94人发生了髋部骨折。使用两个集成模型开发了一种基于机器学习的分阶段模型:集成模型1(仅临床变量)和集成模型2(临床变量和DXA影像学特征)。这种分阶段方法利用集成模型1的不确定性量化来决定DXA特征对于进一步预测是否必要。集成模型2表现出最高的性能,曲线下面积(AUC)为0.9541,准确率为0.9195,灵敏度为0.8078,特异性为0.9427。分阶段模型也表现良好,AUC为0.8486,准确率为0.8611,灵敏度为0.5578,特异性为0.9249,优于集成模型1,集成模型1的AUC为0.5549,准确率为0.7239,灵敏度为0.1956,特异性为0.8343。此外,分阶段模型表明54.49%的患者不需要进行DXA扫描。它有效地平衡了准确率和特异性,在DXA数据采集并非总是可行时提供了一个可靠的解决方案。统计检验证实了各模型之间存在显著差异,突出了先进建模策略的优势。我们的分阶段方法提供了一种具有成本效益的患者健康整体观。它可以高精度地识别有风险的个体,但减少不必要的DXA扫描。我们的方法有望以降低成本和辐射的方式指导预防髋部骨折的干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/46e2a1bd2a3f/nihpp-2405.20071v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/4153dbfcbd85/nihpp-2405.20071v1-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/aae7e1387163/nihpp-2405.20071v1-f0006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/46e2a1bd2a3f/nihpp-2405.20071v1-f0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/4153dbfcbd85/nihpp-2405.20071v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/cdf12f6ff235/nihpp-2405.20071v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/800d67af01e9/nihpp-2405.20071v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/a74c9c3ba9f2/nihpp-2405.20071v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/1129982aa2a7/nihpp-2405.20071v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/aae7e1387163/nihpp-2405.20071v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/9df6077811ef/nihpp-2405.20071v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14dc/11160872/46e2a1bd2a3f/nihpp-2405.20071v1-f0008.jpg

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