TY - JOUR
T1 - Osteoporosis
AU - Baum, Thomas
AU - Karampinos, Dimitrios C.
AU - Ruschke, Stefan
AU - Liebl, Hans
AU - Noël, Peter B.
AU - Bauer, Jan S.
N1 - Publisher Copyright:
© Springer International Publishing Switzerland 2015.
PY - 2015
Y1 - 2015
N2 - Osteoporosis is defined as a skeletal disorder characterized by compromised bone strength predisposing an individual to an increased risk for fracture. Osteoporotic fractures, in particular spine fractures, are associated with a high mortality and generate immense financial costs. Osteoporotic vertebral fractures frequently occur in absence of a specific trauma and may be asymptomatic. Since a prevalent vertebral fracture increases the risk of a subsequent fracture, the diagnosis of osteoporotic vertebral fractures is highly important to initiate appropriate therapy. Computer-assisted diagnostic tools for spine radiographs, dual-energy X-ray absorptiometry (DXA) and multi-detector computed tomography (MDCT) images have been developed to support radiologists to correctly diagnose and report osteoporotic vertebral fractures. The assessment of fracture risk at the spine has traditionally relied on the measurements of bone mineral density (BMD) by using DXA. However, BMD values of subjects with versus without osteoporotic fractures overlap. Bone strength reflects the integration of BMD and bone quality. The latter can be partly determined by measurements of bone microstructure. High-resolution MDCT allows for the assessment of trabecular bone microstructure at the spine. MDCT-based trabecular bone microstructure parameters and finite element models have shown to improve the prediction of bone strength beyond DXA-based BMD and revealed pharmacotherapy effects, which were partly not captured by BMD.
AB - Osteoporosis is defined as a skeletal disorder characterized by compromised bone strength predisposing an individual to an increased risk for fracture. Osteoporotic fractures, in particular spine fractures, are associated with a high mortality and generate immense financial costs. Osteoporotic vertebral fractures frequently occur in absence of a specific trauma and may be asymptomatic. Since a prevalent vertebral fracture increases the risk of a subsequent fracture, the diagnosis of osteoporotic vertebral fractures is highly important to initiate appropriate therapy. Computer-assisted diagnostic tools for spine radiographs, dual-energy X-ray absorptiometry (DXA) and multi-detector computed tomography (MDCT) images have been developed to support radiologists to correctly diagnose and report osteoporotic vertebral fractures. The assessment of fracture risk at the spine has traditionally relied on the measurements of bone mineral density (BMD) by using DXA. However, BMD values of subjects with versus without osteoporotic fractures overlap. Bone strength reflects the integration of BMD and bone quality. The latter can be partly determined by measurements of bone microstructure. High-resolution MDCT allows for the assessment of trabecular bone microstructure at the spine. MDCT-based trabecular bone microstructure parameters and finite element models have shown to improve the prediction of bone strength beyond DXA-based BMD and revealed pharmacotherapy effects, which were partly not captured by BMD.
UR - http://www.scopus.com/inward/record.url?scp=84927516252&partnerID=8YFLogxK
U2 - 10.1007/978-3-319-12508-4_3
DO - 10.1007/978-3-319-12508-4_3
M3 - Article
AN - SCOPUS:84927516252
SN - 2212-9391
VL - 18
SP - 67
EP - 93
JO - Lecture Notes in Computational Vision and Biomechanics
JF - Lecture Notes in Computational Vision and Biomechanics
ER -