Automated bone mineral density prediction and fracture risk assessment using plain radiographs via deep learning
Chen-I Hsieh,
Kang Zheng,
Chihung Lin,
Ling Mei,
Le Lu,
Weijian Li,
Fang-Ping Chen,
Yirui Wang,
Xiaoyun Zhou,
Fakai Wang,
Guotong Xie,
Jing Xiao,
Shun Miao () and
Chang-Fu Kuo ()
Additional contact information
Chen-I Hsieh: Chang Gung Memorial Hospital
Kang Zheng: PAII Inc.
Chihung Lin: Chang Gung Memorial Hospital
Ling Mei: Wuhan Hospital of Traditional Chinese Medicine
Le Lu: PAII Inc.
Weijian Li: PAII Inc.
Fang-Ping Chen: Chang Gung University, Kwei-Shan
Yirui Wang: PAII Inc.
Xiaoyun Zhou: PAII Inc.
Fakai Wang: PAII Inc.
Guotong Xie: Ping An Insurance (Group) Company of China, Ltd.
Jing Xiao: Ping An Insurance (Group) Company of China, Ltd.
Shun Miao: PAII Inc.
Chang-Fu Kuo: Chang Gung Memorial Hospital
Nature Communications, 2021, vol. 12, issue 1, 1-9
Abstract:
Abstract Dual-energy X-ray absorptiometry (DXA) is underutilized to measure bone mineral density (BMD) and evaluate fracture risk. We present an automated tool to identify fractures, predict BMD, and evaluate fracture risk using plain radiographs. The tool performance is evaluated on 5164 and 18175 patients with pelvis/lumbar spine radiographs and Hologic DXA. The model is well calibrated with minimal bias in the hip (slope = 0.982, calibration-in-the-large = −0.003) and the lumbar spine BMD (slope = 0.978, calibration-in-the-large = 0.003). The area under the precision-recall curve and accuracy are 0.89 and 91.7% for hip osteoporosis, 0.89 and 86.2% for spine osteoporosis, 0.83 and 95.0% for high 10-year major fracture risk, and 0.96 and 90.0% for high hip fracture risk. The tool classifies 5206 (84.8%) patients with 95% positive or negative predictive value for osteoporosis, compared to 3008 DXA conducted at the same study period. This automated tool may help identify high-risk patients for osteoporosis.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25779-x
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DOI: 10.1038/s41467-021-25779-x
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