Rapid single‐scan T‐mapping using exponential excitation pulses and image‐based correction for linear background gradients

A method for fast quantitative T mapping based on multiple gradient‐echo (multi‐GE) imaging with correction for static magnetic field inhomogeneities is described, using an exponential excitation pulse. Field gradient maps are obtained from the phase information and modulus data are subsequently corrected, allowing for simple monoexponential T fitting. Echoes with long echo times suffering from major signal losses due to field inhomogeneities are excluded from the analysis. The acquisition time for a matrix size of 256 × 256, 1 mm in‐plane resolution, and 2 mm slice thickness amounts to 15 s per slice. An additional correction for in‐plane field gradients further improves accuracy. Phantom experiments show that the method provides accurate T values for field gradients up to 200 μT/m; for gradients up to 300 μT/m errors do not exceed 15%. In vivo T values acquired on healthy volunteers at 3T are in excellent agreement with results from the literature. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

A technique for rapid single‐echo spin‐echo T2 mapping

A rapid technique for mapping of T₂ relaxation times is presented. The method is based on the conventional single‐echo spin echo approach but uses a much shorter pulse repetition time to accelerate data acquisition. The premise of the new method is the use of a constant difference between the echo time and pulse repetition time, which removes the conventional and restrictive requirement of pulse repetition time ? T₁. Theoretical and simulation investigations were performed to evaluate the criteria for accurate T₂ measurements. Measured T₂s were shown to be within 1% error as long as the key criterion of pulse repetition time/T₂ ≥3 is met. Strictly, a second condition of echo time/T₁ ? 1 is also required. However, violations of this condition were found to have minimal impact in most clinical scenarios. Validation was conducted in phantoms and in vivo T₂ mapping of healthy cartilage and brain. The proposed method offers all the advantages of single‐echo spin echo imaging (e.g., immunity to stimulated echo effects, robustness to static field inhomogeneity, flexibility in the number and choice of echo times) in a considerably reduced amount of time and is readily implemented on any clinical scanner. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Quantitative T*2‐mapping based on multi‐slice multiple gradient echo flash imaging: Retrospective correction for subject motion effects

Numerous clinical and research applications for quantitative mapping of the effective transverse relaxation time T*₂ have been described. Subject motion can severely deteriorate the quality and accuracy of results. A correction method for T*₂ maps acquired with multi‐slice multiple gradient echo FLASH imaging is presented, based on acquisition repetition with reduced spatial resolution (and consequently reduced acquisition time) and weighted averaging of both data sets, choosing weighting factors individually for each k‐space line to reduce the influence of motion. In detail, the procedure is based on the fact that motion artifacts reduce the correlation between acquired and exponentially fitted data. A target data set is constructed in image space, choosing the data yielding best correlation from the two acquired data sets. The k‐space representation of the target is subsequently approximated as linear combination of original raw data, yielding the required weighting factors. As this method only requires a single acquisition repetition with reduced spatial resolution, it can be employed on any clinical system offering a suitable sequence with export of modulus and phase images. Experimental results show that the method works well for sparse motion, but fails for strong motion affecting the same k‐space lines in both acquisitions. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.     

Center‐out echo‐planar spectroscopic imaging with correction of gradient‐echo phase and time shifts

A procedure to prevent the formation of image and spectral Nyquist ghosts in echo‐planar spectroscopic imaging is introduced. It is based on a novel Cartesian center‐out echo‐planar spectroscopic imaging trajectory, referred to as EPSICO, and combined with a correction of the gradient‐echo phase and time shifts. Processing of homogenous sets of forward and reflected echoes is no longer necessary, resulting in an optimized spectral width. The proposed center‐out trajectory passively prevents the formation of Nyquist ghosts by privileging the acquisition of the center k‐space line with forward echoes at the beginning of an echo‐planar spectroscopic imaging dwell time and by ensuring that all k‐space lines and their respective complex conjugates are acquired at equal time intervals. With the proposed procedure, concentrations of N‐acetyl aspartate, creatine, choline, glutamate, and myo‐inositol were reliably determined in human white matter at 3 T. Magn Reson Med, 2013. © 2012 Wiley Periodicals, Inc.     

Correction of main and transmit magnetic field (B0 and B1) inhomogeneity effects in multicomponent‐driven equilibrium single‐pulse observation of T1 and T2

Multicomponent‐driven equilibrium single‐component observation of T₁ and T₂ offers a new approach to multiple component relaxation time and myelin water analysis. The method derives two‐component relaxation information from spoiled and fully balanced steady‐state (SPGR and bSSFP) imaging data acquired over multiple flip angles. Although these steady‐state imaging techniques afford rapid acquisition times and high signal‐to‐noise ratio efficiency, they are also sensitive to main (B₀) and transmit (B₁) magnetic field inhomogeneities. These effects alter the measured signal from their theoretical values and lead to substantive errors in the derived myelin volume fraction estimates. Here, we incorporate correction techniques to mitigate these effects. DESPOT1‐HIFI is used to first calibrate the transmitted flip angles; and B₀ affects are removed through the inclusion of an additional parameter in the multicomponent‐driven equilibrium single‐component observation of T₁ and T₂ fitting, coupled with the acquisition of multiple phase‐cycled bSSFP data. The performance of these correction techniques was evaluated using numerical simulations, demonstrating effective removal of B₀ and B₁‐induced errors in the derived myelin fraction relaxation parameters. The approach was also successfully demonstrated in vivo, with near artifact‐free whole‐brain, high spatial resolution (1.7 mm × 1.7 mm × 1.7 mm isotropic voxels) myelin water fraction maps acquired in a clinically feasible 16 min. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Myocardial T mapping free of distortion using susceptibility‐weighted fast spin‐echo imaging: A feasibility study at 1.5 T and 3.0 T

This study demonstrates the feasibility of applying free‐breathing, cardiac‐gated, susceptibility‐weighted fast spin‐echo imaging together with black blood preparation and navigator‐gated respiratory motion compensation for anatomically accurate T mapping of the heart. First, T maps are presented for oil phantoms without and with respiratory motion emulation (T = (22.1 ± 1.7) ms at 1.5 T and T = (22.65 ± 0.89) ms at 3.0 T). T relaxometry of a ferrofluid revealed relaxivities of R = (477.9 ± 17) mM^?1s^?1 and R = (449.6 ± 13) mM^?1s^?1 for UFLARE and multiecho gradient‐echo imaging at 1.5 T. For inferoseptal myocardial regions mean T values of 29.9 ± 6.6 ms (1.5 T) and 22.3 ± 4.8 ms (3.0 T) were estimated. For posterior myocardial areas close to the vena cava T‐values of 24.0 ± 6.4 ms (1.5 T) and 15.4 ± 1.8 ms (3.0 T) were observed. The merits and limitations of the proposed approach are discussed and its implications for cardiac and vascular T‐mapping are considered. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Multi-gradient echo with susceptibility inhomogeneity compensation (MGESIC): Demonstration of fMRI in the olfactory cortex at 3.0 T

Short image acquisition times and sensitivity to magnetic susceptibility favor the use of gradient echo imaging methods in functional MRI (fMRI). However, magnetic susceptibility effects attributed to air-tissue interfaces also lead to severe signal loss in images of the large inferior frontal and lateral temporal cortices of the human brain, which renders these regions inaccessible to fMRI. The signal loss is caused by the local field gradients in the slice selection direction. A multigradient echo with magnetic susceptibility inhomogeneity compensation method (MGESIC) is proposed to overcome this problem. The MGESIC method effectively corrects the susceptibility artifacts and maintains the advantages of gradient echo methods to both BOLD sensitivity and fast image acquisition. The effectiveness of the MGESIC method is demonstrated by fMRI experimental results within the olfactory cortex.