Abstract

PurposeOsteoporosis is a highly prevalent skeletal disease that frequently entails vertebral fractures. Areal bone mineral density (BMD) derived from dual-energy X-ray absorptiometry (DXA) is the reference standard, but has well-known limitations. Texture analysis can provide surrogate markers of tissue microstructure based on computed tomography (CT) or magnetic resonance imaging (MRI) data of the spine, thus potentially improving fracture risk estimation beyond areal BMD. However, it is largely unknown whether MRI-derived texture analysis can predict volumetric BMD (vBMD), or whether a model incorporating texture analysis based on CT and MRI may be capable of differentiating between patients with and without osteoporotic vertebral fractures.Materials and MethodsTwenty-six patients (15 females, median age: 73 years, 11 patients showing at least one osteoporotic vertebral fracture) who had CT and 3-Tesla chemical shift encoding-based water-fat MRI (CSE-MRI) available were analyzed. In total, 171 vertebral bodies of the thoracolumbar spine were segmented using an automatic convolutional neural network (CNN)-based framework, followed by extraction of integral and trabecular vBMD using CT data. For CSE-MRI, manual segmentation of vertebral bodies and consecutive extraction of the mean proton density fat fraction (PDFF) and T2* was performed. First-order, second-order, and higher-order texture features were derived from texture analysis using CT and CSE-MRI data. Stepwise multivariate linear regression models were computed using integral vBMD and fracture status as dependent variables.ResultsPatients with osteoporotic vertebral fractures showed significantly lower integral and trabecular vBMD when compared to patients without fractures (p<0.001). For the model with integral vBMD as the dependent variable, T2* combined with three PDFF-based texture features explained 40% of the variance (adjusted R2 = 0.40; p<0.001). Furthermore, regarding the differentiation between patients with and without osteoporotic vertebral fractures, a model including texture features from CT and CSE-MRI data showed better performance than a model based on integral vBMD and PDFF only ( = 0.47 vs. = 0.81; included texture features in the final model: integral vBMD, CT_Short-run_emphasis, CT_Varianceglobal, and PDFF_Variance).ConclusionUsing texture analysis for spine CT and CSE-MRI can facilitate the differentiation between patients with and without osteoporotic vertebral fractures, implicating that future fracture prediction in osteoporosis may be improved.

Highlights

  • In clinical routine, assessment of areal bone mineral density (BMD) and the individual risk of bone fracture is commonly obtained using dual-energy X-ray absorptiometry (DXA) [1,2,3,4]

  • We used texture analysis on computed tomography (CT) and chemical shift encoding-based water-fat Magnetic resonance imaging (MRI) (CSE-MRI) data covering the thoracolumbar spine in patients with and without osteoporotic vertebral fractures to predict Volumetric BMD (vBMD), and to discriminate between patients with and without osteoporotic vertebral fractures based on models including vBMD, proton density fat fraction (PDFF), T2*, and texture features

  • The main findings are as follow: first, a model including T2* combined with three PDFF-based texture features explained 40% of the variance in integral vBMD; second, a model consisting of integral vBMD and three texture features (CT_SRE, CT_Varianceglobal, and PDFF_Variance) explained 81% of the variance regarding the osteoporotic vertebral fracture status, compared to 47% when the model was based on integral vBMD and PDFF only

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Summary

Introduction

Assessment of areal bone mineral density (BMD) and the individual risk of bone fracture is commonly obtained using dual-energy X-ray absorptiometry (DXA) [1,2,3,4]. Vertebral fractures are prevalent, with an estimated 12.6-fold increase in the risk of future additional vertebral fractures [1, 11,12,13]. A major clinical issue of these fractures is that they occur frequently but can remain asymptomatic for a long time [13, 14]. This can delay diagnosis, timely treatment initiation, and subsequent approaches to avoid future additional osteoporotic vertebral fractures [13, 14]

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