TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
TRADITIONAL POSTER - ismrm
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Poster Sessions<br />
1766. Combined Assessment of Vascular Territories and Haemodynamic Parameter Maps<br />
Rebecca Susan Dewey 1,2 , Dorothee P. Auer 1 , Susan T. Francis 2<br />
1 Division of Academic Radiology, University of Nottingham, Nottingham, Nottinghamshire, United Kingdom; 2 Sir Peter Mansfield<br />
Magnetic Resonance Centre, University of Nottingham, Nottingham, Nottinghamshire, United Kingdom<br />
Watershed areas are brain regions supplied by the most distal branches of the cerebral arteries and are most susceptible to haemodynamic ischaemia. We<br />
assess the use of territorial ASL to define Left and Right Internal Carotid, Anterior Cerebral, and Basilar Artery territories to distinguish the watershed area,<br />
and assess its correspondence with haemodynamic parameters (perfusion rate, arterial blood volume and arterial and tissue transit times) from multiphase<br />
ASL. Specified anatomical regions are assessed for vascular supply and haemodynamic parameters. Combining these techniques, an atlas of parameters can<br />
be formed for region-specific perfusion and position and functional effects of watershed areas.<br />
1767. Simultaneous Measurements of Arterial Transit Times and Water Exchange Rates by Diffusion-<br />
Weighted ASL<br />
Keith S. St. Lawrence 1,2 , Jodi Miller 1 , Jiongjiong Wang 3<br />
1 Imaging, Lawson Health Research Institute, London, ON, Canada; 2 Medical Biophysics, University of Western Ontario, London,<br />
ON, Canada; 3 Radiology, University of Pennsylvania, Philadelphia, PA, United States<br />
The arterial transit time (τa) and the exchange rate of water (kw) across the blood-brain barrier were determined using diffusion-weighted arterial spin<br />
labelling (ASL) with multiple post-labelling delay times. τa was determined using bipolar gradients to suppress the arterial signal (i.e., the FEAST method)<br />
and kw was determined using bipolar gradients strong enough to suppress all vascular signals and a kinetic model to characterize water exchange across the<br />
BBB. Averaged over four volunteers, kw was 119 min-1 in grey matter and τa was 1.26 s. From repeat measurements, the intra-subject coefficient of<br />
variation of kw was 12%.<br />
1768. Flow-Weighted Arterial Transit Time Mapping of the Human Brain<br />
Toralf Mildner 1 , Stefan Hetzer 1 , Wolfgang Driesel 1 , Karsten Müller 1 , Harald E. Möller 1<br />
1 NMR unit, Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Saxony, Germany<br />
Mapping of Arterial Transit times by Intravascular Signal SElection (MATISSE) was performed with and without a mild flow-weighting (FW). The arterial<br />
transit times, δa , of the flow-weighted data were increased on average by about 700 ms and the signal amplitudes roughly were halved. Flow-through signals,<br />
i. e. signals of arterial vessels permeating the voxel, are removed almost completely, although the MATISSE signal still is expected to be of vascular origin.<br />
The fact that δa with mild FW was found to be easily larger than 2 s might be important for the quantification of CBF in standard dual-coil CASL<br />
experiments.<br />
1769. Arterial Transit Delay Measurement Using Pseudo-Continuous ASL with Variable TR and Interleaved<br />
Post-Labeling Delays<br />
Kun Lu 1 , Thomas T. Liu 1 , Youngkyoo Jung 1<br />
1 Center for Functional MRI, UCSD, La Jolla, CA, United States<br />
Conventional arterial transit delay measurements consist of a series of separate ASL experiments acquired at several different post-labeling delays. Such<br />
measurements are usually time-consuming and can be formidable overheads for ASL studies. The time requirement also makes the measurements highly<br />
sensitive to motion. This study presents a simple yet effective modification of the conventional method for measuring transit delay with shorter scan time<br />
and less motion sensitivity. Such a method could be beneficial to all ASL studies.<br />
1770. Eliminating the Partition Coefficient from ASL Perfusion Quantification with a Homogeneous<br />
Contrast Reference Image<br />
Weiying Dai 1 , Philip M. Robson 1 , Ajit Shankaranarayanan 2 , David C. Alsop 1<br />
1 Radiology, Beth Israel Deaconess Medical Center,Harvard Medical School, Boston, MA, United States; 2 Global Applied Science<br />
Laboratory, GE Healthcare, Menlo Park, CA, United States<br />
Conventional ASL perfusion quantification requires division by a proton density reference image and assumes a uniform brain-blood partition coefficient.<br />
The brain-blood partition coefficient is not constant, however, and may especially differ in areas of pathology. In cortical regions where CSF, white matter<br />
and gray matter may all be mixed within a voxel, division by the proton density image can also add nonlinear systematic errors. Here we propose using an<br />
optimized inversion preparation to generate an image whose intensity is essentially independent of tissue type. This highly homogeneous image can replace<br />
the proton density image and makes the assumption of a brain-blood partition coefficient unnecessary. In-vivo results demonstrate that such homogeneous<br />
contrast is achievable and can be used to improve the pixel-by-pixel perfusion measurement.<br />
1771. Potential Tracking of Oxygen Consumption Using Arterial Spin Labeling Susceptibility Imaging<br />
Johannes Gregori 1,2 , Norbert Schuff 3,4 , Matthias Günther 1,5<br />
1 Institute for Medical Image Computing, Fraunhofer MEVIS, Bremen, Germany; 2 Neurology, Universitätsmedizin Mannheim,<br />
Heidelberg University, Mannheim, Germany; 3 Radiology & Biomedical Imaging, University of San Francisco, San Francisco, CA,<br />
United States; 4 Center for Imaging of Neurodegenerate Diseases (CIND), VA Medical Center, San Francisco, CA, United States;<br />
5 mediri GmbH, Heidelberg, Germany<br />
We present ASL time series measurements with spin/gradient double echo spiral 3D-GRASE readout to quantify R2' of the ASL difference signal. R2' can<br />
give information about blood oxygenation and blood volume, while ASL time series are used to investigate perfusion dynamics. Using the combination of<br />
both techniques, we can measure the changes of R2' over different inflow times and discuss the physiological underlyings.