QCT-based finite element models predict human vertebral strength in vitro significantly better than simulated DEXA

被引:155
作者
Dall'Ara, E. [1 ]
Pahr, D. [1 ]
Varga, P. [1 ]
Kainberger, F. [2 ]
Zysset, P. [1 ]
机构
[1] Vienna Univ Technol, Inst Lightweight Design & Struct Biomech, A-1040 Vienna, Austria
[2] Med Univ Vienna, Dept Radiol, A-1090 Vienna, Austria
关键词
Finite element modeling; Bone mineral density; DXA; Bone strength; Osteoporosis; Mechanical testing; QUANTITATIVE COMPUTED-TOMOGRAPHY; BONE STRENGTH; TRABECULAR BONE; MECHANICAL-PROPERTIES; CORTICAL BONE; DENSITY; FRACTURE; OSTEOPOROSIS; BIOMECHANICS; ARCHITECTURE;
D O I
10.1007/s00198-011-1568-3
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
While dual energy X-ray absorptiometry (DXA) is considered the gold standard to evaluate fracture risk in vivo, in the present study, the quantitative computed tomography (QCT)-based finite element modeling has been found to provide a quantitative and significantly improved prediction of vertebral strength in vitro. This technique might be used in vivo considering however the much larger doses of radiation needed for QCT. Vertebral fracture is a common medical problem in osteoporotic individuals. Bone mineral density (BMD) is the gold standard measure to evaluate fracture risk in vivo. QCT-based finite element (FE) modeling is an engineering method to predict vertebral strength. The aim of this study was to compare the ability of FE and clinical diagnostic tools to predict vertebral strength in vitro using an improved testing protocol. Thirty-seven vertebral sections were scanned with QCT and high resolution peripheral QCT (HR-pQCT). Bone mineral content (BMC), total BMD (tBMD), areal BMD from lateral (aBMD-lat), and anterior-posterior (aBMD-ap) projections were evaluated for both resolutions. Wedge-shaped fractures were then induced in each specimen with a novel testing setup. Nonlinear homogenized FE models (hFE) and linear micro-FE (mu FE) were generated from QCT and HR-pQCT images, respectively. For experiments and models, both structural properties (stiffness, ultimate load) and material properties (apparent modulus and strength) were computed and compared. Both hFE and mu FE models predicted material properties better than structural ones and predicted strength significantly better than aBMD computed from QCT and HR-pQCT (hFE: RA(2) = 0.79, mu FE: RA(2) = 0.88, aBMD-ap: RA(2) = 0.48-0.47, aBMD-lat: RA(2)aEuro parts per thousand= 0.41-0.43). Moreover, the hFE provided reasonable quantitative estimations of the experimental mechanical properties without fitting the model parameters. The QCT-based hFE method provides a quantitative and significantly improved prediction of vertebral strength in vitro when compared to simulated DXA. This superior predictive power needs to be verified for loading conditions that simulate even more the in vivo case for human vertebrae.
引用
收藏
页码:563 / 572
页数:10
相关论文
共 58 条
[1]
Bone strength and its determinants [J].
Ammann, P ;
Rizzoli, R .
OSTEOPOROSIS INTERNATIONAL, 2003, 14 (Suppl 3) :S13-S18
[2]
A scalable multi-level preconditioner for matrix-free μ-finite element analysis of human bone structures [J].
Arbenz, Peter ;
van Lenthe, G. Harry ;
Mennel, Uche ;
Mueller, Ralph ;
Sala, Marzio .
INTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN ENGINEERING, 2008, 73 (07) :927-947
[3]
The role of cortical bone and its microstructure in bone strength [J].
Augat, Peter ;
Schorlemmer, Sandra .
AGE AND AGEING, 2006, 35 :27-31
[4]
A comparison of spinal quantitative computed tomography with dual energy X-ray absorptiometry in European women with vertebral and nonvertebral fractures [J].
Bergot, C ;
Laval-Jeantet, AM ;
Hutchinson, K ;
Dautraix, I ;
Caulin, F ;
Genant, HK .
CALCIFIED TISSUE INTERNATIONAL, 2001, 68 (02) :74-82
[5]
Alendronate increases bone strength by increasing the mean degree of mineralization of bone tissue in osteoporotic women [J].
Boivin, GY ;
Chavassieux, PM ;
Santora, AC ;
Yates, J ;
Meunier, PJ .
BONE, 2000, 27 (05) :687-694
[6]
Bone quality: where do we go from here? [J].
Bouxsein, ML .
OSTEOPOROSIS INTERNATIONAL, 2003, 14 (Suppl 5) :S118-S127
[7]
Allometric scaling and biomechanical behavior of the bone tissue: An experimental intraspecific investigation [J].
Brianza, Stefano Z. M. ;
D'Amelio, Patrizia ;
Pugno, Nicola ;
Delise, Marco ;
Bignardi, Cristina ;
Isaia, Giancarlo .
BONE, 2007, 40 (06) :1635-1642
[8]
Comparison of quantitative computed tomography-based measures in predicting vertebral compressive strength [J].
Buckley, Jenni M. ;
Loo, Kenneth ;
Motherway, Julie .
BONE, 2007, 40 (03) :767-774
[9]
Automated simulation of areal bone mineral density assessment in the distal radius from high-resolution peripheral quantitative computed tomography [J].
Burghardt, A. J. ;
Kazakia, G. J. ;
Link, T. M. ;
Majumdar, S. .
OSTEOPOROSIS INTERNATIONAL, 2009, 20 (12) :2017-2024
[10]
A patient-specific finite element methodology to predict damage accumulation in vertebral bodies under axial compression, sagittal flexion and combined loads [J].
Chevalier, Yan ;
Charlebois, Mathieu ;
Pahr, Dieter ;
Varga, Peter ;
Heini, Paul ;
Schneider, Erich ;
Zysset, Philippe .
COMPUTER METHODS IN BIOMECHANICS AND BIOMEDICAL ENGINEERING, 2008, 11 (05) :477-487