TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
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Poster Sessions<br />
1569. White Matter Model for Diffusional Kurtosis Imaging<br />
Els Fieremans 1 , Jens H. Jensen 1 , Ali Tabesh 1 , Caixia Hu 1,2 , Joseph A. Helpern 1,2<br />
1 Radiology, New York University School of Medicine, New York, United States; 2 Center for Advanced Brain Imaging, Nathan S.<br />
Kline Institute, Orangeburg, NY, United States<br />
We develop an idealized two-compartment diffusion model of white matter suitable for analysis with diffusional kurtosis imaging (DKI). The standard DKI<br />
metrics are used to derive the extracellular and axonal bare diffusion coefficients, the axonal water fraction (AWF), and tortuosity of the extra-axonal<br />
geometry, both providing information related to axonal and myelin density. Values for these parameters obtained for a healthy volunteer agree well with<br />
those of prior studies. Since a DKI dataset is acquired within a few minutes, this approach may allow for the clinical assessment of myelin associated<br />
neuropathologies, such as multiple sclerosis and Alzheimer’s disease.<br />
1570. A Mechanism for Exchange Between Intraaxonal and Extracellular Water: Permeable Nodes of<br />
Ranvier<br />
Markus Nilsson 1 , Håkan Hagslätt 2,3 , Danielle van Westen 2,3 , Ronnie Wirestam 1 , Freddy Ståhlberg 1,3 , Jimmy<br />
Lätt 1,2<br />
1 Department of Medical Radiation Physics, Lund University, Lund, Sweden; 2 Center for Medical Imaging and Physiology, Lund<br />
University Hospital, Lund, Sweden; 3 Department of Diagnostic Radiology, Lund University, Lund, Sweden<br />
The axonal water exchange time was investigated in Monte Carlo simulations using impermeable myelin sheaths, but permeable nodes of Ranvier. The<br />
results showed that axonal exchange times on the sub-second were possible for short and intermediate internodal lengths (i.e. length of the myelin sheath)<br />
and high nodal permeability. This is of importance for high b-value diffusion MRI when measured with different diffusion times.<br />
1571. Renormalization Group Method: Influence of Packing Density of Axons on Diffusivity in Enhanced<br />
Basser-Sen Model of the Brain White Matter<br />
Oleg P. Posnansky 1 , N. J. Shah 2,3<br />
1 Institute of Neuroscience and Medicine - 4, Medical Imaging Physics, Forschungszentrum Juelich, GmbH, 52425 Juelich, Germany;<br />
2 Institute of Neuroscience and Medicine - 4, Medical Imaging Physics , Forschungszentrum Juelich, GmbH , 52425 Juelich, Germany;<br />
3 Deparment of Neurology, Faculty of Medicine, RWTH Aachen University, 52074 Aachen, Germany<br />
Diffusion weighted MRI is sensitive to tissue architecture on a micrometer scale. Determining whether it is possible to infer the specific mechanisms that<br />
underlie changes in the DW-MRI could lead to new diffusion contrasts specific to particular white-matter degeneration processes. We have developed a<br />
renormalization-group method in order to explore the effects of a large range of microparameters on apparent-diffusion and applied it to different kind of<br />
brain tissue tessellations. Our approach takes the influence of disorder into the consideration and it allows quantitative investigation of the sensitivity of<br />
apparent-diffusion to the variations of the dominant set of microparameters.<br />
1572. Observation of Anisotropy at Different Length Scales in Optic and Sciatic Nerve Speciments<br />
Evren Ozarslan 1 , N Shemesh 2 , Y Cohen 2 , Peter J. Basser<br />
1 NIH, Bethesda, MD, United States; 2 Tel Aviv University<br />
Double-PFG MR is a promising method to assess restriction induced anisotropy at different length scales enabling the extraction of information such as<br />
compartment size, shape, and orientation distribution function. In this work, we present the simultaneous characterization of the axon diameter and the<br />
dispersion in the orientation of the axons in excised optic and sciatic nerve specimens. Assuming a von Mises distribution for the orientation distribution<br />
function enabled the characterization of the dispersion of fiber orientations via the estimation of only one additional parameter.<br />
1573. Random Walks in the Model Brain Tissue: Monte Carlo Simulations and Implications for Diffusion<br />
Imaging<br />
Farida Grinberg 1 , Yuliya Kupriyanova 1 , Ana-Maria Oros-Peusquens 1 , N Jon Shah 1,2<br />
1 Medical Imaging Physics, Institute of Neuroscience and Medicine 4, Forschungszentrum Juelich GmbH, Juelich, Germany;<br />
2 Department of Neurology, Faculty of Medicine, RWTH Aachen University, Aachen, Germany<br />
The propagation of water molecules in the brain and the corresponding NMR response are affected by many factors such as compartmentalization,<br />
restrictions, and anisotropy imposed by the cellular microstructure. In addition, interfacial interactions with the cell membranes and exchange play a role.<br />
Therefore, a differentiation between the various contributions to the average NMR signal in in vivo studies represents a difficult task. In this work, we have<br />
performed random-walk Monte Carlo simulations in model systems aiming at establishing the quantitative relations between the dynamics and<br />
microstructure. A detailed analysis of the average diffusion propagators and the corresponding signal attenuations is presented and the implications for<br />
experimental studies are discussed.<br />
1574. Discovering White Matter Structure Beyond Fractional Anisotropy Maps<br />
Jakub Piatkowski 1 , Amos J. Storkey 2 , Mark E. Bastin 3<br />
1 Neuroinformatics Doctoral Training Centre, University of Edinburgh, Edinburgh, United Kingdom; 2 Institute for Adaptive and<br />
Neural Computation, School of Informatics, University of Edinburgh, Edinburgh, United Kingdom; 3 Medical Physics, University of<br />
Edinburgh, Edinburgh, Midlothian, United Kingdom<br />
We use a fully physical two-compartment model, comprising isotropic and anisotropic terms, to describe diffusion MRI data. The posterior distributions<br />
over the parameters of this model are estimated using sampling techniques. This yields maps of white matter (WM) volume, which reveal a level of structure<br />
missing in FA maps. Additionally, we get tensor parameters for the anisotropic compartment (i.e. WM), which provide a measure of fibre-specific<br />
anisotropy that doesn't suffer from partial volume effects.