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The Predictive Role of Skeletal Density and Porosity in Fracture Risk
13 10 月, 2025From: BSD Instrument
Introduction
Fractures, particularly osteoporotic fractures, represent a major global health concern due to their association with morbidity, mortality, and healthcare costs. Accurate prediction of fracture risk is essential for early intervention and prevention. While bone mineral density (BMD) has long been the gold standard for assessing fracture risk, emerging evidence highlights the importance of bone microarchitecture, particularly skeletal porosity, as an additional—and sometimes more sensitive—predictor. This article explores how skeletal density and porosity contribute to fracture risk prediction.
Background: Bone Density and Porosity
Bone Mineral Density (BMD): Measured primarily via Dual-energy X-ray Absorptiometry (DXA), BMD reflects the amount of mineral content per unit volume of bone. Low BMD is strongly associated with increased fracture risk, as seen in osteoporosis.
Skeletal Porosity: Refers to the presence of microscopic pores or voids within trabecular and cortical bone. Increased porosity weakens bone structure, reducing its load-bearing capacity even when BMD appears normal.
While BMD provides a macroscopic measure of bone strength, porosity offers insights into microstructural integrity, making it a complementary predictor.
Mechanisms Linking Density and Porosity to Fracture Risk
Bone Strength Depends on Both Density and Structure
BMD contributes to bone’s resistance to compression but does not account for trabecular connectivity or cortical thickness.
Porosity (especially in cortical bone) reduces bone stiffness and increases susceptibility to microcracks, leading to fractures under lower stress.
Cortical Porosity and Age-Related Bone Loss
With aging, cortical bone (the dense outer shell) undergoes endosteal resorption, increasing porosity.
Even in individuals with normal BMD, high cortical porosity can lead to fragility fractures (e.g., hip, wrist).
Trabecular Bone Microarchitecture
Trabecular bone (found in vertebrae and ends of long bones) relies on trabecular thickness and connectivity.
Increased trabecular spacing (a form of porosity) reduces structural support, raising vertebral fracture risk.
Clinical Relevance: Beyond DXA
DXA Limitations: While DXA-based BMD predicts fractures, it misses microarchitectural deterioration.
Advanced Imaging Techniques:
High-resolution peripheral quantitative computed tomography (HR-pQCT) and micro-CT assess porosity and trabecular structure.
Trabecular Bone Score (TBS) evaluates bone texture from DXA images, indirectly reflecting microarchitecture.
Predictive Power: Studies show that high cortical porosity is an independent risk factor for fractures, even in patients with normal or osteopenic BMD.
Conclusion
While skeletal density (BMD) remains a cornerstone in fracture risk assessment, skeletal porosity—particularly in cortical and trabecular bone—provides critical additional information. Advanced imaging techniques that evaluate microarchitecture and porosity can improve fracture prediction, especially in individuals with normal BMD but high fracture risk. Future clinical guidelines may incorporate porosity metrics alongside BMD for more precise risk stratification.
Key Takeaways:
✅ BMD alone is insufficient—porosity affects bone strength independently.✅ Cortical porosity increases fracture risk, even with normal BMD.✅ Advanced imaging (HR-pQCT, TBS) helps assess porosity for better fracture prediction.
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