{"title":"Predicting skeletal age from HR-pQCT imaging","authors":"Annabel R. Bugbird , Steven K. Boyd","doi":"10.1016/j.bone.2025.117761","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction:</h3><div>High-resolution peripheral quantitative computed tomography (HR-pQCT) provides detailed bone microarchitecture assessments, but the interpretability of its many complex parameters remains challenging. This study aimed to develop a deep learning model to estimate skeletal age from HR-pQCT scans, offering an interpretable, quantitative summary of bone health relative to chronological age.</div></div><div><h3>Methods:</h3><div>The <em>training</em> dataset included 1236 adults (62.1% female) from a normative cohort, and an independent <em>test</em> set of 460 adults (69.3% female). HR-pQCT scans of the distal radius and tibia were acquired for all participants. Five models were trained: 2D models using a single radius (<em>2DRad</em>) and tibia (<em>2DTib</em>) slice from the middle of the scan; 3D models using full volumetric radius (<em>3DRad</em>) and tibia (<em>3DTib</em>); and a combined 2D model (<em>2DRadTib</em>) applying linear regression to the 2D outputs.</div></div><div><h3>Results:</h3><div>The <em>2DRadTib</em> model achieved the best performance, with a <em>validation</em> mean absolute error (MAE) of 5.29 ± 4.60 years (R<span><math><msup><mrow></mrow><mrow><mn>2</mn></mrow></msup></math></span> = 0.85) and <em>test</em> MAE of 5.34 ± 4.38 years (R<span><math><msup><mrow></mrow><mrow><mn>2</mn></mrow></msup></math></span> = 0.85). Saliency maps revealed cortical bone was most influential in younger individuals, while both cortical and trabecular features contributed in older participants. Predicted skeletal age was strongly correlated with established HR-pQCT parameters, particularly cortical and density measures (<span><math><mi>ρ</mi></math></span> = –0.51 to 0.85), indicating the model relies on key bone features.</div></div><div><h3>Conclusion:</h3><div>We present a novel deep learning framework for skeletal age prediction from HR-pQCT, providing a concise and interpretable summary measure of bone health. This approach may enhance the clinical utility of HR-pQCT by improving interpretability and supporting early identification of accelerated skeletal aging.</div></div><div><h3>Lay Summary</h3><div>High-resolution peripheral quantitative computed tomography (HR-pQCT) provides detailed images of bone structure, but the volume and complexity of data can make interpretation difficult. In this study, we developed a deep learning model to estimate skeletal age from HR-pQCT scans, offering a simplified and interpretable measure of bone health. By translating complex imaging data into an age-based summary, this approach may enhance clinical use of HR-pQCT, support early identification of individuals at risk of accelerated bone loss, and improve patient understanding by providing a relatable measure of skeletal integrity.</div></div>","PeriodicalId":9301,"journal":{"name":"Bone","volume":"204 ","pages":"Article 117761"},"PeriodicalIF":3.9000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bone","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S8756328225003734","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/13 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction:
High-resolution peripheral quantitative computed tomography (HR-pQCT) provides detailed bone microarchitecture assessments, but the interpretability of its many complex parameters remains challenging. This study aimed to develop a deep learning model to estimate skeletal age from HR-pQCT scans, offering an interpretable, quantitative summary of bone health relative to chronological age.
Methods:
The training dataset included 1236 adults (62.1% female) from a normative cohort, and an independent test set of 460 adults (69.3% female). HR-pQCT scans of the distal radius and tibia were acquired for all participants. Five models were trained: 2D models using a single radius (2DRad) and tibia (2DTib) slice from the middle of the scan; 3D models using full volumetric radius (3DRad) and tibia (3DTib); and a combined 2D model (2DRadTib) applying linear regression to the 2D outputs.
Results:
The 2DRadTib model achieved the best performance, with a validation mean absolute error (MAE) of 5.29 ± 4.60 years (R = 0.85) and test MAE of 5.34 ± 4.38 years (R = 0.85). Saliency maps revealed cortical bone was most influential in younger individuals, while both cortical and trabecular features contributed in older participants. Predicted skeletal age was strongly correlated with established HR-pQCT parameters, particularly cortical and density measures ( = –0.51 to 0.85), indicating the model relies on key bone features.
Conclusion:
We present a novel deep learning framework for skeletal age prediction from HR-pQCT, providing a concise and interpretable summary measure of bone health. This approach may enhance the clinical utility of HR-pQCT by improving interpretability and supporting early identification of accelerated skeletal aging.
Lay Summary
High-resolution peripheral quantitative computed tomography (HR-pQCT) provides detailed images of bone structure, but the volume and complexity of data can make interpretation difficult. In this study, we developed a deep learning model to estimate skeletal age from HR-pQCT scans, offering a simplified and interpretable measure of bone health. By translating complex imaging data into an age-based summary, this approach may enhance clinical use of HR-pQCT, support early identification of individuals at risk of accelerated bone loss, and improve patient understanding by providing a relatable measure of skeletal integrity.
期刊介绍:
BONE is an interdisciplinary forum for the rapid publication of original articles and reviews on basic, translational, and clinical aspects of bone and mineral metabolism. The Journal also encourages submissions related to interactions of bone with other organ systems, including cartilage, endocrine, muscle, fat, neural, vascular, gastrointestinal, hematopoietic, and immune systems. Particular attention is placed on the application of experimental studies to clinical practice.