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      Combination of Nanoindentation and Quantitative Backscattered Electron Imaging Revealed Altered Bone Material Properties Associated with Femoral Neck Fragility

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          Abstract

          Osteoporotic fragility fractures were hypothesized to be related to changes in bone material properties and not solely to reduction in bone mass. We studied cortical bone from the superior and inferior sectors of whole femoral neck sections from five female osteoporotic hip fracture cases (74–92 years) and five nonfractured controls (75–88 years). The typical calcium content (Ca Peak) and the mineral particle thickness parameter (T) were mapped in large areas of the superior and inferior regions using quantitative backscattered electron imaging (qBEI) and scanning small-angle X-ray scattering, respectively. Additionally, indentation modulus (E) and hardness (H) (determined by nanoindentation) were compared at the local level to the mineral content (Ca Ind) at the indent positions (obtained from qBEI). Ca Peak (−2.2%, P = 0.002), Ca Ind (−1.8%, P = 0.048), E (−5.6%, P = 0.040), and H (−6.0%, P = 0.016) were significantly lower for the superior compared to the inferior region. Interestingly, Ca Peak as well as Ca Ind were also lower (−2.6%, P = 0.006, and –3.7%, P = 0.002, respectively) in fracture cases compared to controls, while E and H did not show any significant reduction. T values were in the normal range, independent of region ( P = 0.181) or fracture status ( P = 0.551). In conclusion, it appears that the observed femoral neck fragility is associated with a reduced mineral content, which was not accompanied by a reduction in stiffness and hardness of the bone material. This pilot study suggests that a stiffening process in the organic matrix component contributes to bone fragility independently of mineral content.

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          An improved technique for determining hardness and elastic modulus using load and displacement sensing indentation experiments

          The indentation load-displacement behavior of six materials tested with a Berkovich indenter has been carefully documented to establish an improved method for determining hardness and elastic modulus from indentation load-displacement data. The materials included fused silica, soda–lime glass, and single crystals of aluminum, tungsten, quartz, and sapphire. It is shown that the load–displacement curves during unloading in these materials are not linear, even in the initial stages, thereby suggesting that the flat punch approximation used so often in the analysis of unloading data is not entirely adequate. An analysis technique is presented that accounts for the curvature in the unloading data and provides a physically justifiable procedure for determining the depth which should be used in conjunction with the indenter shape function to establish the contact area at peak load. The hardnesses and elastic moduli of the six materials are computed using the analysis procedure and compared with values determined by independent means to assess the accuracy of the method. The results show that with good technique, moduli can be measured to within 5%.
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            Two-dimensional detector software: From real detector to idealised image or two-theta scan

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              Diagnosis of osteoporosis and assessment of fracture risk.

              John Kanis (2002)
              The diagnosis of osteoporosis centres on the assessment of bone mineral density (BMD). Osteoporosis is defined as a BMD 2.5 SD or more below the average value for premenopausal women (T score < -2.5 SD). Severe osteoporosis denotes osteoporosis in the presence of one or more fragility fractures. The same absolute value for BMD used in women can be used in men. The recommended site for diagnosis is the proximal femur with dual energy X-ray absorptiometry (DXA). Other sites and validated techniques, however, can be used for fracture prediction. Although hip fracture prediction with BMD alone is at least as good as blood pressure readings to predict stroke, the predictive value of BMD can be enhanced by use of other factors, such as biochemical indices of bone resorption and clinical risk factors. Clinical risk factors that contribute to fracture risk independently of BMD include age, previous fragility fracture, premature menopause, a family history of hip fracture, and the use of oral corticosteroids. In the absence of validated population screening strategies, a case finding strategy is recommended based on the finding of risk factors. Treatment should be considered in individuals subsequently shown to have a high fracture risk. Because of the many techniques available for fracture risk assessment, the 10-year probability of fracture is the desirable measurement to determine intervention thresholds. Many treatments can be provided cost-effectively to men and women if hip fracture probability over 10 years ranges from 2% to 10% dependent on age.
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                Author and article information

                Contributors
                barbara.misof@osteologie.at
                Journal
                Calcif Tissue Int
                Calcified Tissue International
                Springer-Verlag (New York )
                0171-967X
                1432-0827
                12 September 2009
                October 2009
                : 85
                : 4
                : 335-343
                Affiliations
                [1 ]Ludwig Boltzmann Institute of Osteology, Hanusch Hospital of WGKK and AUVA Trauma Center Meidling, 4th Medical Department, Hanusch Hospital, 1140 Vienna, Austria
                [2 ]Department of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany
                [3 ]Erich Schmid Institute of Materials Science, Austrian Academy of Sciences and Institute of Metal Physics, University of Leoben, 8700 Leoben, Austria
                [4 ]Bone Research Division, Department of Medicine, University of Cambridge, Cambridge, CB2 2QQ UK
                [5 ]Ludwig Boltzmann Institute of Osteology, UKH Meidling, Kundratstrasse 37, A-1120 Vienna, Austria
                [6 ]Laboratoire de Physique des Solides, Université Paris-Sud, Bat. 510, 91405 Orsay cedex, France
                Article
                9289
                10.1007/s00223-009-9289-8
                2759010
                19756347
                767f6b7d-d7b2-4036-b8ae-8915d6323948
                © The Author(s) 2009
                History
                : 29 April 2009
                : 2 August 2009
                Categories
                Article
                Custom metadata
                © Springer Science+Business Media, LLC 2009

                Human biology
                osteoporosis,nanoindentation,small-angle x-ray scattering,quantitative backscattered electron imaging,femoral neck

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