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Open AccessJournal ArticleDOI

High-resolution T1 mapping of the brain at 3T with driven equilibrium single pulse observation of T1 with high-speed incorporation of RF field inhomogeneities (DESPOT1-HIFI)

Sean C.L. Deoni
- 01 Oct 2007 - 
- Vol. 26, Iss: 4, pp 1106-1111
TLDR
An alternative approach to correct for flip angle inaccuracies in the driven equilibrium single pulse observation of T1 (DESPOT1) T1 mapping method is investigated.
Abstract
Purpose To investigate an alternative approach to correct for flip angle inaccuracies in the driven equilibrium single pulse observation of T1 (DESPOT1) T1 mapping method. Materials and Methods While DESPOT1 is a robust method for rapid whole-brain voxelwise mapping of the longitudinal relaxation time, the approach is inherently sensitive to inaccuracies in the transmitted flip angle, defined by the B1 field, which become more severe with increased field. Here we propose an extension of the DESPOT1 technique, involving the additional acquisition of an inversion-prepared SPGR image alongside the conventional multiangle DESPOT1 data. From these combined data both B1 and T1 may be determined with high accuracy and precision. The method is evaluated at 3T with phantom and in vivo imaging experiments, with derived T1 estimates compared with values calculated from multiple inversion time inversion recovery data. Results The method provides robust correction of flip angle variations, with less than 5% error compared with reference values for T1 between 300 msec and 2500 msec. Conclusions The described approach, dubbed DESPOT1-HIFI, permits whole-brain T1 mapping at 3T, with 1 mm3 isotropic voxels, in a clinically feasible time (≈10 minutes) with T1 accuracy greater than 5% and with high precision. J. Magn. Reson. Imaging 2007;26:1106–1111. © 2007 Wiley-Liss, Inc.

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Citations
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MP2RAGE, a self bias-field corrected sequence for improved segmentation and T1-mapping at high field

TL;DR: The MPRAGE sequence was modified to generate two different images at different inversion times, MP2RAGE, to create T(1)-weighted images where the result image was free of proton density contrast, T(2) contrast, reception bias field, and, to first order, transmit field inhomogeneity.
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Gleaning multicomponent T1 and T2 information from steady-state imaging data.

TL;DR: The multicomponent driven equilibrium single-pulse observation of T(1)/T(2) (mcDESPOT) was proposed in this article to characterize the longitudinal and transverse relaxation times of the human white matter and gray matter.
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Characterization of cerebral white matter properties using quantitative magnetic resonance imaging stains.

TL;DR: Three quantitative MRI methods for characterizing white matter (WM) microstructural properties are reviewed, all of which measure complementary aspects of how water interacts with the tissue environment.
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References
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Journal ArticleDOI

T1, T2 relaxation and magnetization transfer in tissue at 3T

TL;DR: The results provide a useful reference for optimization of pulse sequence parameters for MRI at 3 T and the phenomenological MT parameter, magnetization transfer ratio, MTR, was lower by approximately 2 to 10%.
Journal ArticleDOI

7T vs. 4T: RF power, homogeneity, and signal-to-noise comparison in head images.

TL;DR: Signal‐to‐noise ratio (SNR), RF field (B1), and RF power requirement for human head imaging were examined at 7T and 4T magnetic field strengths and were consistent with calculations performed using a human head model and Maxwell's equations.
Journal ArticleDOI

Rapid combined T1 and T2 mapping using gradient recalled acquisition in the steady state.

TL;DR: The method permits real‐time clinical acquisition and display of whole brain T1 and T2 maps for the first time and represents the most efficient of those examined.
Journal ArticleDOI

Spiral-in/out BOLD fMRI for increased SNR and reduced susceptibility artifacts.

TL;DR: The use of spiral‐in trajectories that begin at the edge of k‐space and end at the origin, and spiral in/out trajectories in which a spiral‐ in readout is followed by a conventional spiral‐out trajectory are reported.
Journal ArticleDOI

Imaging of the active B1 field in vivo.

TL;DR: With the described method the active B1 field can be determined in vivo in 23 cross‐sections in less than 6 min, and the stability and accuracy of the presented method is shown by several phantom and in vivo measurements.
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