Stroke is the third most frequent cause of mortality in western society. Recent progress in the field of ischernic stroke has shown that thrombolysis treatment increases survival and reduces disability, but that early intervention is the key to successful therapeutic outcome. Because treatment also poses risks in terms of increased chance of hemorrhage, it is essential to determine whether reversible or irreversible damage has occured during and after ischernic periods. Magnetic Resonance Imaging (MRI) and Spectroscopy (MRS) hold great promise for noninvasive assessment of brain damage. In addition to assessing large- vessel and small-vessel perfusion using MR angiography (MRA) and dynamic contrast imaging, respectively, the occurrence of a mismatch between diffusion and perfusion abnormalities has been used as an indicator for need for treatment. Even though this has met with some success to extend the treatment window from 3 to 6 or even more hours post-ictus, the exact meaning of the diffusion and perfusion deficits remains a point of discussion and there is a general consensus that a multi-parameter assessment of different flow and metabolic zones in the ischernic region would enhance the specificity of the MR assessment. The ultimate goal of our research is to establish a set of MRI criteria that will allow such an assessment. Towards this end our research has focused on the development of new functional imaging methods that can quantitatively assess tissue status when neurologic recovery is still possible. Based on results obtained in the previous grant period, we have designed the following hypotheses for ischernic stroke: (1) The area of hypoperfusion that has reduced pH predicts the area that will go to infarction if no treatment is initiated; (2) The area of increased microvascular cerebral blood volume (CBV) is a marker for tissue at risk of infarction. (3) quantification of oxygen extraction fraction (OEF) can predict the risk for tissue infarction based on the principle of flow thresholds. Our corresponding three aims are to develop new noninvasive MRI methodologies that are sensitive to changes in pH, CBV, and OEF and to subsequently test our three hypothesis on rat brain models of transient focal ischemia. Our fourth and final aim is to implement the new technologies on the clinical scanner and to optimize their use for a fast and specific clinical stroke exam.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB002634-13
Application #
7126467
Study Section
Biomedical Imaging Technology Study Section (BMIT)
Program Officer
Mclaughlin, Alan Charles
Project Start
1992-06-10
Project End
2009-07-31
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
13
Fiscal Year
2006
Total Cost
$359,322
Indirect Cost
Name
Johns Hopkins University
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Qin, Qin; Strouse, John J; van Zijl, Peter C M (2011) Fast measurement of blood T1 in the human jugular vein at 3 Tesla. Magn Reson Med 65:1297-304
Qin, Qin; Grgac, Ksenija; van Zijl, Peter C M (2011) Determination of whole-brain oxygen extraction fractions by fast measurement of blood T(2) in the jugular vein. Magn Reson Med 65:471-9
Zhou, Jinyuan (2011) Amide proton transfer imaging of the human brain. Methods Mol Biol 711:227-37
Hua, Jun; Qin, Qin; Pekar, James J et al. (2011) Measurement of absolute arterial cerebral blood volume in human brain without using a contrast agent. NMR Biomed 24:1313-25
Qin, Qin (2011) A simple approach for three-dimensional mapping of baseline cerebrospinal fluid volume fraction. Magn Reson Med 65:385-91
Hua, Jun; Qin, Qin; Donahue, Manus J et al. (2011) Inflow-based vascular-space-occupancy (iVASO) MRI. Magn Reson Med 66:40-56
Kim, Mina; Gillen, Joseph; Landman, Bennett A et al. (2009) Water saturation shift referencing (WASSR) for chemical exchange saturation transfer (CEST) experiments. Magn Reson Med 61:1441-50
Zhou, Jinyuan; Blakeley, Jaishri O; Hua, Jun et al. (2008) Practical data acquisition method for human brain tumor amide proton transfer (APT) imaging. Magn Reson Med 60:842-9
Salhotra, Amandeep; Lal, Bachchu; Laterra, John et al. (2008) Amide proton transfer imaging of 9L gliosarcoma and human glioblastoma xenografts. NMR Biomed 21:489-97
Sun, Phillip Zhe (2007) Improved diffusion measurement in heterogeneous systems using the magic asymmetric gradient stimulated echo (MAGSTE) technique. J Magn Reson 187:177-83

Showing the most recent 10 out of 21 publications