Abstract

Background Areal bone mineral density is predictive for fracture risk. Microstructural bone parameters evaluated at the appendicular skeleton by high-resolution peripheral quantitative computed tomography (HR-pQCT) display differences between healthy patients and fracture patients. With the simple geometry of the cortex at the distal tibial diaphysis, a cortical index of the tibia combining material and mechanical properties correlated highly with bone strength ex vivo. The trabecular bone score derived from the scan of the lumbar spine by dual-energy X-ray absorptiometry (DXA) correlated ex vivo with the micro architectural parameters. It is unknown if these microstructural correlations could be made in healthy premenopausal women. Methods Randomly selected women between 20–40 years of age were examined by DXA and HR-pQCT at the standard regions of interest and at customized sub regions to focus on cortical and trabecular parameters of strength separately. For cortical strength, at the distal tibia the volumetric cortical index was calculated directly from HR-pQCT and the areal cortical index was derived from the DXA scan using a Canny threshold-based tool. For trabecular strength, the trabecular bone score was calculated based on the DXA scan of the lumbar spine and was compared with the corresponding parameters derived from the HR-pQCT measurements at radius and tibia. Results Seventy-two healthy women were included (average age 33.8 years, average BMI 23.2 kg/m2). The areal cortical index correlated highly with the volumetric cortical index at the distal tibia (R = 0.798). The trabecular bone score correlated moderately with the microstructural parameters of the trabecular bone. Conclusion This study in randomly selected premenopausal women demonstrated that microstructural parameters of the bone evaluated by HR-pQCT correlated with the DXA derived parameters of skeletal regions containing predominantly cortical or cancellous bone. Whether these indexes are suitable for better predictions of the fracture risk deserves further investigation.

Highlights

  • In addition to low bone mass, osteoporosis was characterized in the WHO Technical Report of 1994 [1] by the micro architectural deterioration of bone tissue

  • The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

  • Driven by sex steroid hormone levels changing with aging, the structures of the long bones are altered by enhanced endosteal resorption and are only in part compensated by periosteal apposition [2]

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Summary

Introduction

In addition to low bone mass, osteoporosis was characterized in the WHO Technical Report of 1994 [1] by the micro architectural deterioration of bone tissue. Driven by sex steroid hormone levels changing with aging, the structures of the long bones are altered by enhanced endosteal resorption and are only in part compensated by periosteal apposition [2] This change translates into altered micro architecture of the trabecular and cortical bone in vivo as assessed by high resolution imaging techniques, such as high-resolution peripheral quantitative computed tomography (HR-pQCT) [3]. The trabecular bone score derived from the scan of the lumbar spine by dual-energy X-ray absorptiometry (DXA) correlated ex vivo with the micro architectural parameters. It is unknown if these microstructural correlations could be made in healthy premenopausal women

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