## Abstract The application of __T__~1~ in the rotating frame (__T__~1ρ~) to functional MRI in humans was studied at 3 T. Increases in neural activity increased parenchymal __T__~1ρ~. Modeling suggested that cerebral blood volume mediated this increase. A pulse sequence named spin‐locked echo plana
Magnetic resonance imaging with T1 dispersion contrast
✍ Scribed by Sharon E. Ungersma; Nathaniel I. Matter; Jonathan W. Hardy; Ross D. Venook; Albert Macovski; Steven M. Conolly; Greig C. Scott
- Book ID
- 102952817
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 736 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0740-3194
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Prepolarized MRI uses pulsed magnetic fields to produce MR images by polarizing the sample at one field strength (∼0.5 T) before imaging at a much lower field (∼50 mT). Contrast reflecting the T~1~ of the sample at an intermediate field strength is achieved by polarizing the sample and then allowing the magnetization to decay at a chosen “evolution” field before imaging. For tissues whose T~1~ varies with field strength (T~1~ dispersion), the difference between two images collected with different evolution fields yields an image with contrast reflecting the slope of the T~1~ dispersion curve between those fields. Tissues with high protein content, such as muscle, exhibit rapid changes in their T~1~ dispersion curves at 49 and 65 mT due to cross‐relaxation with nitrogen nuclei in protein backbones. Tissues without protein, such as fat, have fairly constant T~1~ over this range; subtracting images with two different evolution fields eliminates signal from flat T~1~ dispersion species. T~1~ dispersion protein‐content images of the human wrist and foot are presented, showing clear differentiation between muscle and fat. This technique may prove useful for delineating regions of muscle tissue in the extremities of patients with diseases affecting muscle viability, such as diabetic neuropathy, and for visualizing the protein content of tissues in vivo. Magn Reson Med 2006. © 2006 Wiley‐Liss, Inc.
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