TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
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Poster Sessions<br />
793. Characterization of Trabecular Orientation in Chicken Femur by Multi-Directional SPENT (Sub-Pixel<br />
Enhancement of Non-Uniform Tissue)<br />
Bailiang Chen 1 , Bernard Siow 2 , David Carmichael 1,3 , Freddy Odille 2 , Roger Ordidge 1 , Andrew Todd-<br />
Pokropek 1<br />
1 Medical Physics and Bioengineering, University College London, London, United Kingdom; 2 Centre for Medical Image Computing,<br />
University College London, London, United Kingdom; 3 Institute of Neurology , University College London, London, United<br />
Kingdom<br />
The recently proposed SPENT sequence can provide direction specific information based on the sub-voxel structural uniformity of a sample. Analogous to<br />
diffusion tensor imaging, given a voxel with a local anisotropic structure (e.g. trabecular bone), it is possible to characterize the orientation of sub-pixel<br />
micro-structure by applying SPENT with multiple directions. A 6-direction SPENT series was applied to a chicken femur head in order to characterize its<br />
trabecular bone orientation by reconstructing a 2D tensor in each voxel. Both tensor statistics and eigensystems were computed and showed good qualitative<br />
agreement with data from a subsequent micro-CT acquisitions.<br />
794. The Effect of Freezing on Measurements of Trabecular Bone Structure Based on NMR Spectroscopy<br />
Viktoria Prantner 1 , Hanna Isaksson 1 , Johanna Närväinen 2 , Eveliina Lammentausta 3 , Olli HJ Gröhn 2,4 ,<br />
Jukka S. Jurvelin 1<br />
1 Department of Physics, University of Kuopio, Kuopio, Finland; 2 A.I. Virtanen Institute for Molecular Sciences, University of<br />
Kuopio, Kuopio, Finland; 3 Department of Diagnostic Radiology, Oulu University Hospital, Oulu, Finland; 4 Biomedical Imaging Unit,<br />
University of Kuopio, Kuopio, Finland<br />
NMR is a potential tool for the assessment of trabecular bone structure. Since trabecular bone provides a negligible NMR signal, the indirect evaluation of<br />
the trabecular bone structure is based on the analysis of water and fat components in the bone marrow. Earlier studies have revealed that freezing affects the<br />
bone marrow structure, suggesting there may be changes in the molecular structure. The aim of the current study is to investigate the effect of freezing on<br />
trabecular bone and bone marrow, as assessed by NMR spectroscopy.<br />
795. Performance of Two Spin-Echo Sequences for Quantitative Structure Analysis of Trabecular Bone<br />
Michael Jeffrey Wald 1 , Jeremy Francis Magland 1 , X. Edward Guo 2 , Felix Werner Wehrli 1<br />
1 Laboratory for Structural NMR Imaging, University of Pennsylvania Medical Center, Philadelphia, PA, United States; 2 Bone<br />
Bioengineering Laboratory, Columbia University, New York, United States<br />
The performance of two spin-echo based pulse sequences for imaging trabecular bone microstructure are evaluated at 1.5T in seven fixed, cadaveric distal<br />
tibia specimens. SNR efficiency and sensitivity of image-derived trabecular bone structural parameters to variations in bone quality as assessed by µCT were<br />
investigated. Inter- pulse sequence correlations suggest similar structural sensitivity, while comparisons to µCT reveal good sensitivity but large deviations<br />
in absolute values between modalities.<br />
796. Ultra-Short TE (UTE) Imaging of Skull and a Quantitative Comparison of Skull Images Obtained<br />
from MRI and CT<br />
Liya Wang 1 , Xiaodong Zhong 2 , Longjiang Zhang 3 , Diana Tiwari 1 , Hui Mao 1<br />
1 Department of Radiology and Emory Center for Systems Imaging, Emory University School of Medicine, Atlanta, GA, United<br />
States; 2 MR R&D Collaborations, Siemens healthcare, Atlanta, GA, United States; 3 Department of Radiology, Jinlin Hospital and<br />
Nanjing University College of Clinical Medicine, Nanjing, Jiangsu, China<br />
This study provided a quantitative evaluation of skull images obtained using UTE MRI and a direct comparison to those from CT. The skull thickness<br />
measured from UTE images showed good agreement with those obtained from CT images in different slices. There is also a good correlation between the<br />
thickness measurements obtained from CT and UTE images. Signal intensity based evaluation showed that there is no statistical difference between UTE<br />
and CT images in outer, inner layer and diploe of the skull. The comparison of bone UTE MRI and CT of skull suggests that UTE images match closely with<br />
CT images.<br />
797. MR Imaging Detects Impaired Angiogenesis and Trabecular Bone Formation During Endochondral<br />
Bone Growth Mediated Through PKBalpha/Akt1 in Gene Dosage Dependent Manner<br />
Katrien Vandoorne 1 , Jeremy Magland 2 , Vicki Plaks 1 , Inbal E. Biton 3 , Amnon Sharir 4,5 , Elazar Zelzer 4 ,<br />
Felix Wehrli 6 , Brian A. Hemmings 7 , Alon Harmelin 3 , Michal Neeman 1<br />
1 Biological Regulation, Weizmann Institute, Rehovot, Israel; 2 Department of Radiology, University of Pennsylvania Health System,<br />
Philadelphia, PA, United States; 3 Veterinary Resources, Weizmann Institute, Rehovot, Israel; 4 Molecular Genetics, Weizmann<br />
Institute, Rehovot, Israel; 5 The Laboratory of Musculoskeletal Biomechanics and Applied Anatomy, Koret School of Veterinary Medi,<br />
Hebrew University of Jerusalem, Rehovot, Israel; 6 Department of Radiology, University of Pennsylvania Health System, Philadelphia,<br />
PA, Israel; 7 Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland<br />
Since infiltration of the newly formed blood vessels is required for endochondral bone formation, and PKBalpha/Akt1 mediates intracellular signaling of<br />
angiogenesis, we postulated that a vascular deficiency at the site of the long bones could contribute indirectly to impaired bone development in<br />
PKBalpha/Akt1 deficient mice. Our study demonstrated using macromolecular DCE-MRI in vivo and ex vivo µCT and µMRI, vascular and bone<br />
developmental defects in PKBalpha/Akt1 null mice, and remarkably also in heterozygous mice, lacking a single copy of the gene.