DIfferential Subsampling with Cartesian Ordering (DISCO): a high spatio-temporal resolution Dixon imaging sequence for multiphasic contrast enhanced abdominal imaging

Purpose:

To develop and evaluate a multiphasic contrast‐enhanced MRI method called DIfferential Sub‐sampling with Cartesian Ordering (DISCO) for abdominal imaging.

Materials and Methods:

A three‐dimensional, variable density pseudo‐random k‐space segmentation scheme was developed and combined with a Dixon‐based fat‐water separation algorithm to generate high temporal resolution images with robust fat suppression and without compromise in spatial resolution or coverage. With institutional review board approval and informed consent, 11 consecutive patients referred for abdominal MRI at 3 Tesla (T) were imaged with both DISCO and a routine clinical three‐dimensional SPGR‐Dixon (LAVA FLEX) sequence. All images were graded by two radiologists using quality of fat suppression, severity of artifacts, and overall image quality as scoring criteria. For assessment of arterial phase capture efficiency, the number of temporal phases with angiographic phase and hepatic arterial phase was recorded.

Results:

There were no significant differences in quality of fat suppression, artifact severity or overall image quality between DISCO and LAVA FLEX images (P > 0.05, Wilcoxon signed rank test). The angiographic and arterial phases were captured in all 11 patients scanned using the DISCO acquisition (mean number of phases were two and three, respectively).

Conclusion:

DISCO effectively captures the fast dynamics of abdominal pathology such as hyperenhancing hepatic lesions with a high spatio‐temporal resolution. Typically, 1.1 × 1.5 × 3 mm spatial resolution over 60 slices was achieved with a temporal resolution of 4–5 s. J. Magn. Reson. Imaging 2012;35:1484–1492. © 2012 Wiley Periodicals, Inc.     

High Speed 1H Spectroscopic Imaging in Human Brain by Echo Planar Spatial-Spectral Encoding

We introduce a fast and robust spatial-spectral encoding method, which enables acquisition of high resolution short echo time (13 ms) proton spectroscopic images from human brain with acquisition times as short as 64 s when using surface coils. The encoding scheme, which was implemented on a clinical 1.5 Tesla whole body scanner, is a modification of an echo-planar spectroscopic imaging method originally proposed by Mansfield Magn. Reson. Med. 1, 370–386 (1984), and utilizes a series of read-out gradients to simultaneously encode spatial and spectral information. Superficial lipid signals are suppressed by a novel double outer volume suppression along the contours of the brain. The spectral resolution and the signal-to-noise per unit time and unit volume from resonances such as N-acetyl aspartate, choline, creatine, and inositol are comparable with those obtained with conventional methods. The short encoding time of this technique enhances the flexibility of in vivo spectroscopic imaging by reducing motion artifacts and allowing acquisition of multiple data sets with different parameter settings.     

3D 31P Spectroscopic Imaging of the Human Heart at 4.1 T

High field (4 Tesla) spectroscopic imaging offers the advantages of increased signal-to-noise ratio and the possibility of acquiring high resolution metabolite images. We have applied a three dimensional spectroscopic imaging sequence using a sparse Gaussian sampling method to acquire phosphocreatine (PCr) images of the human heart with 8-cc voxels. PCr images enabled observation of the septum, left ventricular free wall, apex, and skeletal muscle. Quantitative evaluation of the 50 myocardial voxels acquired from 10 studies of healthy adults revealed a PCr/adenosine triphosphate (ATP) ratio of 1.80 ± 0.32 after correction for saturation effects. Due to the small size of the voxels and the ability to choose the location of the volumes to minimize inclusion of blood, no correction for blood pool ATP was required. The calculated PCr/ATP ratio is in agreement with other studies at 1.5 and 4.0 T.     

Diffusion-weighted whole-body MR imaging with background body signal suppression: a feasibility study at 3.0 Tesla

The purpose was to provide a diffusion-weighted whole-body magnetic resonance (MR) imaging sequence with background body signal suppression (DWIBS) at 3.0 Tesla. A diffusion-weighted spin-echo echo-planar imaging sequence was combined with the following methods of fat suppression: short TI inversion recovery (STIR), spectral attenuated inversion recovery (SPAIR), and spectral presaturation by inversion recovery (SPIR). Optimized sequences were implemented on a 3.0- and a 1.5-Tesla system and evaluated in three healthy volunteers and six patients with various lesions in the neck, chest, and abdomen on the basis of reconstructed maximum intensity projection images. In one patient with metastases of malignant melanoma, DWIBS was compared with ¹⁸F-fluorodeoxyglucose positron emission tomography (FDG-PET). Good fat suppression for all regions and diagnostic image quality in all cases could be obtained at 3.0 Tesla with the STIR method. In comparison with 1.5 Tesla, DWIBS images at 3.0 Tesla were judged to provide a better lesion-to-bone tissue contrast. However, larger susceptibility-induced image distortions and signal intensity losses, stronger blurring artifacts, and more pronounced motion artifacts degraded the image quality at 3.0 Tesla. A good correlation was found between the metastases as depicted by DWIBS and those as visualized by FDG-PET. DWIBS is feasible at 3.0 Tesla with diagnostic image quality.     

Inversion recovery with embedded self‐calibration (IRES)

With self‐calibrated parallel acquisition, the calibration data used to characterize coil response are acquired within the actual, parallel scan. Although this eliminates the need for a separate calibration scan, it reduces the net acceleration factor of the parallel scan. Furthermore, this reduction gets worse at higher accelerations. A method is described for three‐dimensional inversion recovery gradient‐echo imaging in which calibration is incorporated into the sequence but with no loss of net acceleration. This is done by acquiring the calibration data using very small (≤4°) tip angle acquisitions during the delay interval after acquisition of the accelerated imaging data. The technique is studied at 3 Tesla with simulation, phantom, and in vivo experiments using both image‐space‐based and k‐space‐based parallel reconstruction methods. At nominal acceleration factors of 3 and 4, the newly described inversion recovery with embedded self‐calibration (IRES) method can retain effective acceleration with comparable SNR and contrast to standard self‐calibration. At a net two‐dimensional acceleration factor of 4, IRES can achieve higher SNR than standard self‐calibration having a nominal acceleration factor of 6 but the same acquisition time. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Geodesic topological analysis of trabecular bone microarchitecture from high‐spatial resolution magnetic resonance images

In vivo assessment of trabecular bone microarchitecture could improve the prediction of fracture risk and the efficacy of osteoporosis treatment and prevention. Geodesic topological analysis (GTA) is introduced as a novel technique to quantify the trabecular bone microarchitecture from high‐spatial resolution magnetic resonance (MR) images. Trabecular bone parameters that quantify the scale, topology, and anisotropy of the trabecular bone network in terms of its junctions are the result of GTA. The reproducibility of GTA was tested with in vivo images of human distal tibiae and radii (n = 6) at 1.5 Tesla; and its ability to discriminate between subjects with and without vertebral fracture was assessed with ex vivo images of human calcanei at 1.5 and 3.0 Tesla (n = 30). GTA parameters yielded an average reproducibility of 4.8%, and their individual areas under the curve (AUC) of the receiver operating characteristic curve analysis for fracture discrimination performed better at 3.0 than at 1.5 Tesla reaching values of up to 0.78 (p < 0.001). Logistic regression analysis demonstrated that fracture discrimination was improved by combining GTA parameters, and that GTA combined with bone mineral density (BMD) allow for better discrimination than BMD alone (AUC = 0.95; p < 0.001). Results indicate that GTA can substantially contribute in studies of osteoporosis involving imaging of the trabecular bone microarchitecture. Magn Reson Med 61:448–456, 2009. © 2009 Wiley‐Liss, Inc.     

High resolution three‐dimensional cardiac perfusion imaging using compartment‐based k‐t principal component analysis

Three‐dimensional myocardial perfusion imaging requires significant acceleration of data acquisition to achieve whole‐heart coverage with adequate spatial and temporal resolution. The present article introduces a compartment‐based k‐t principal component analysis reconstruction approach, which permits three‐dimensional perfusion imaging at 10‐fold nominal acceleration. Using numerical simulations, it is shown that the compartment‐based method results in accurate representations of dynamic signal intensity changes with significant improvements of temporal fidelity in comparison to conventional k‐t principal component analysis reconstructions. Comparison of the two methods based on rest and stress three‐dimensional perfusion data acquired with 2.3 × 2.3 × 10 mm³ during a 225 msec acquisition window in patients confirms the findings and demonstrates the potential of compartment‐based k‐t principal component analysis for highly accelerated three‐dimensional perfusion imaging. Magn Reson Med, 2011. © 2010 Wiley‐Liss, Inc.     

4D retrospective black blood trueFISP imaging of mouse heart

The purpose of this study was to demonstrate the feasibility of steady‐state True fast imaging with steady precession (TrueFISP) four‐dimensional imaging of mouse heart at high resolution and its efficiency for cardiac volumetry. Three‐dimensional cine‐imaging of control and hypoxic mice was carried out at 4.7 T without magnetization preparation or ECG‐triggering. The k‐space lines were acquired with the TrueFISP sequence (pulse repetition time/echo time = 4/2 ms) in a repeated sequential manner. Retrospective reordering of raw data allowed the reconstruction of 10 three‐dimensional images per cardiac cycle. The acquisition scheme used an alternating radiofrequency phase and sum‐of‐square reconstruction method. Black‐blood three‐dimensional images at around 200 μm resolution were produced without banding artifact throughout the cardiac cycle. High contrast to noise made it possible to estimate cavity volumes during diastole and systole. Right and left ventricular stroke volume was significantly higher in hypoxic mice vs controls (20.2 ± 2 vs 15.1 ± 2; P < 0.05, 24.9 ± 2 vs 20.4 ± 2; P < 0.05, respectively). In conclusion, four‐dimensional black‐blood TrueFISP imaging in living mice is a method of choice to investigate cardiac abnormalities in mouse models. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

A comparison of MR cholangiopancreatography at 1.5 and 3.0 Tesla

Clinical MR systems operating at 3.0 Tesla have the potential to significantly improve spatial resolution due to the boost in intrinsic signal to noise ratio. However, body imaging at these field strengths presents a number of technical challenges. We performed a prospective pilot study in which 10 patients underwent an MR cholangiopancreatography (MRCP) examination consecutively on 1.5 and 3.0 Tesla systems (both Philips Intera). An axial half Fourier segmented turbo spin echo (HASTE) sequence and a coronal thick-slab 2D turbo-spin echo (TSE) sequence were compared on both systems. A reader measured the signal intensity (SI) ratios of common bile duct (CBD): liver, and CBD: fat on HASTE images and CBD: liver on the TSE images. A second reader performed a qualitative analysis of the intrahepatic and extrahepatic biliary anatomy. Quantitative data was compared using the paired t-test and qualitative data with the paired Wilcoxon signed rank test with p < 0.05. The quantitative analysis of the HASTE sequences showed a slightly higher signal intensity ratio (CBD:liver) at 3.0 Tesla compared with 1.5 Tesla (8.1 vs 5.6, p = 0.002). No significant difference was found between the SI ratios of (CBD:fat) on HASTE images or (CBD:liver) on TSE images. The qualitative analysis showed superior image quality of 3.0 Tesla over 1.5 Tesla images on both HASTE (31 vs 25, p = 0.032), and TSE sequences (34 vs 28, p = 0.043). This pilot study shows that MRCP is feasible at 3.0 Tesla with some improvement in image quality and signal characteristics. Further development may be achieved with sequence optimization and improved coil design.     

MR cholangiopancreatography: comparison of images obtained with 1.0 and 1.5 Tesla units

OBJECTIVE: To compare the image quality and visualization obtained in MR cholangiopancreatography (MRCP) using different high-field strength (1.0 vs. 1.5 Tesla) MR units and to assess the effect of field strength on MRCP. MATERIALS AND METHODS: This study population included 10 healthy volunteers and 37 patients suspected of having pancreatobiliary diseases. MRCP images were obtained using two MR units with different high-field strengths (1.0 and 1.5 Tesla), with half-Fourier acquisition single-shot turbo spin-echo (HASTE) and rapid acquisition by relaxation enhancement (RARE) sequences. The image quality and visualization of each portion of the pancreatobiliary system were graded and recorded using a four-point scale. Additionally, the signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) were measured. RESULTS: The SNR and CNR in HASTE sequences acquired with the 1.5 Tesla (T) unit were significantly higher than those acquired with the 1.0 T unit (p=0.001). In qualitative analysis, there were no statistically significant differences in image quality or visualization of the ducts in either HASTE or RARE sequences between 1.0 T and 1.5 T. CONCLUSION: Our study showed that visual image quality provided by MRCP was equivalent at 1.0 and 1.5 T.     

Three-dimensional late gadolinium enhancement imaging of the left atrium with a hybrid radial acquisition and compressed sensing

Purpose:

To develop and test a hybrid radial (stack of stars) acquisition and compressed sensing reconstruction for efficient late gadolinium enhancement (LGE) imaging of the left atrium.

Materials and Methods:

Two hybrid radial acquisition schemes, kx‐ky‐first and kz‐first, are tested using the signal equation for an inversion recovery sequence with simulated data. Undersampled data reconstructions are then performed using a compressed sensing approach with a three‐dimensional total variation constraint. The data acquisition and reconstruction framework is tested on five atrial fibrillation patients after treatment by radio‐frequency ablation. The hybrid radial data are acquired with free breathing without respiratory navigation.

Results:

The kz‐first radial acquisition gave improved image quality as compared to a kx‐ky‐first scheme. Compressed sensing reconstructions improved the overall quality of undersampled radial LGE images. An image quality metric that takes into account the signal, noise, artifact, and blur for the radial images was 35% (±17%) higher than the corresponding Cartesian acquisitions. Total acquisition time for 36 slices with 1.25 × 1.25 × 2.5 mm³ resolution was under 3 min for the proposed scheme.

Conclusion:

Hybrid radial LGE imaging of the LA with compressed sensing is a promising approach for obtaining images efficiently and offers more robust image quality than Cartesian acquisitions that were acquired without a respiratory navigator signal. J. Magn. Reson. Imaging 2011;. © 2011 Wiley Periodicals, Inc.     

Three‐dimensional mapping of the B1 field using an optimized phase‐based method: Application to hyperpolarized 3He in lungs

A novel method is presented for the three‐dimensional mapping of the B₁‐field of a transmit radio‐frequency MR coil. The method is based on the acquisition of phase images, where the effective flip angle is encoded in the phase of the nonselective hard pulse excitation. The method involves the application of a rectangular composite pulse as excitation in a three‐dimensional gradient recall echo to produce measurable phase angle variation. However, such a pulse may significantly increase the radio‐frequency power deposition in excess of the standard acceptable SAR limits, imposing extremely long TRs (>100 msec), which would result in acquisition times significantly greater than a single breath‐hold. In this study, the phases of the radio‐frequency excitation are modified, resulting in a different pulse sequence scheme. It is shown that the new method increases sensitivity with respect to radio‐frequency inhomogeneities by up to 10 times, and reduces the total duration of the pulse so that three‐dimensional B₁ mapping is possible with ³He in lungs within a single breath‐hold. Computer simulations demonstrate the increase in sensitivity. Phantom results with ¹H MRI are used for validation. In vivo results are presented with hyperpolarized ³He in human lungs at 1.5T. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Three-Dimensional Spectroscopic Imaging with Time-Varying Gradients

A spectroscopic imaging sequence with a time-varying readout gradient in the slice selection direction is used to image multiple contiguous slices. For a given voxel size, the imaging time and signal-to-noise ratio of the three-dimensional spectroscopic sequence are the same as for a single slice acquisition without the oscillating readout gradient. The data reconstruction employs a gridding algorithm in two dimensions to interpolate the nonuniformly sampled data onto a Cartesian grid, and a fast Fourier transform in four dimensions: three spatial dimensions and the spectral dimension. The method is demonstrated by in vivo imaging of NAA in human brain at 1.5 T with 10 slices of 16 x 16 pixels spectroscopic images acquired in a total scan time of 17 min.     

Mapping of redox status in a brain‐disease mouse model by three‐dimensional EPR imaging

Electron paramagnetic resonance imaging using nitroxides is a powerful method for visualizing the redox status modulated by oxidative stress in vivo. Typically, however, data acquisition times have been too slow to obtain a sufficient number of projections for three‐dimensional images, when using continuous wave‐electron paramagnetic resonance imager in small rodents, using nitroxides with comparatively short T₂ and a half‐life values. Because of improvements in imagers that enable rapid data‐acquisition, the feasibility of three‐dimensional electron paramagnetic resonance imaging with good quality in mice was tested with nitroxides. Three‐dimensional images of mice were obtained at an interval of 15 sec under field scanning of 0.3 sec and with 46 projections in the case of strong electron paramagnetic resonance signals. Three‐dimensional electron paramagnetic resonance images of a blood brain barrier‐permeable nitroxide, 3‐hydroxymethyl‐2,2,5,5‐tetramethylpyrrolidine‐1‐oxyl, in the mouse head clearly showed that 3‐hydroxymethyl‐2,2,5,5‐tetramethylpyrrolidine‐1‐oxyl was distributed within brain tissues, and this was confirmed by MRI observations. Based on the pharmacokinetics of nitroxides in mice, half‐life mapping was demonstrated in an ischemia‐reperfusion model mouse brain. Inhomogeneous half‐lives were clearly mapped pixel‐by‐pixel in mouse head under oxidative stress by the improved continuous wave‐electron paramagnetic resonance imager noninvasively. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

High-resolution proton density weighted three-dimensional fast spin echo (3D-FSE) of the knee with IDEAL at 1.5 Tesla: comparison with 3D-FSE and 2D-FSE--initial experience

Purpose:

To assess the feasibility of combining three‐dimensional fast spin echo (3D‐FSE) and Iterative‐decomposition‐of water‐and‐fat‐with‐echo asymmetry‐and‐least‐squares‐estimation (IDEAL) at 1.5 Tesla (T), generating a high‐resolution 3D isotropic proton density‐weighted image set with and without “fat‐suppression” (FS) in a single acquisition, and to compare with 2D‐FSE and 3D‐FSE (without IDEAL).

Materials and Methods:

Ten asymptomatic volunteers prospectively underwent sagittal 3D‐FSE‐IDEAL, 3D‐FSE, and 2D‐FSE sequences at 1.5T (slice thickness [ST]: 0.8 mm, 0.8 mm, and 3.5 mm, respectively). 3D‐FSE and 2D‐FSE were repeated with frequency‐selective FS. Fluid, cartilage, and muscle signal‐to‐noise ratio (SNR) and fluid‐cartilage contrast‐to‐noise ratio (CNR) were compared among sequences. Three blinded reviewers independently scored quality of menisci/cartilage depiction for all sequences. “Fat‐suppression” was qualitatively scored and compared among sequences.

Results:

3D‐FSE‐IDEAL fluid‐cartilage CNR was higher than in 2D‐FSE (P < 0.05), not different from 3D‐FSE (P = 0.31). There was no significant difference in fluid SNR among sequences. 2D‐FSE cartilage SNR was higher than in 3D FSE‐IDEAL (P < 0.05), not different to 3D‐FSE (P = 0.059). 2D‐FSE muscle SNR was higher than in 3D‐FSE‐IDEAL (P < 0.05) and 3D‐FSE (P < 0.05). Good or excellent depiction of menisci/cartilage was achieved using 3D‐FSE‐IDEAL in the acquired sagittal and reformatted planes. Excellent, homogeneous “fat‐suppression” was achieved using 3D‐FSE‐IDEAL, superior to FS‐3D‐FSE and FS‐2D‐FSE (P < 0.05).

Conclusion:

3D FSE‐IDEAL is a feasible approach to acquire multiplanar images of diagnostic quality, both with and without homogeneous “fat‐suppression” from a single acquisition. J. Magn. Reson. Imaging 2012;361‐369. © 2011 Wiley Periodicals, Inc.     

1H spectroscopic imaging of human brain at 3 Tesla: Comparison of fast three‐dimensional magnetic resonance spectroscopic imaging techniques

Purpose

To investigate the signal‐to‐noise‐ratio (SNR) and data quality of time‐reduced three‐dimensional (3D) proton magnetic resonance spectroscopic imaging (¹H MRSI) techniques in the human brain at 3 Tesla.

Materials and Methods

Techniques that were investigated included ellipsoidal k‐space sampling, parallel imaging, and echo‐planar spectroscopic imaging (EPSI). The SNR values for N‐acetyl aspartate, choline, creatine, and lactate or lipid peaks were compared after correcting for effective spatial resolution and acquisition time in a phantom and in the brains of human volunteers. Other factors considered were linewidths, metabolite ratios, partial volume effects, and subcutaneous lipid contamination.

Results

In volunteers, the median normalized SNR for parallel imaging data decreased by 34–42%, but could be significantly improved using regularization. The normalized signal to noise loss in flyback EPSI data was 11–18%. The effective spatial resolutions of the traditional, ellipsoidal, sensitivity encoding (SENSE) sampling scheme, and EPSI data were 1.02, 2.43, 1.03, and 1.01 cm³, respectively. As expected, lipid contamination was variable between subjects but was highest for the SENSE data. Patient data obtained using the flyback EPSI method were of excellent quality.

Conclusion

Data from all ¹H 3D‐MRSI techniques were qualitatively acceptable, based upon SNR, linewidths, and metabolite ratios. The larger field of view obtained with the EPSI methods showed negligible lipid aliasing with acceptable SNR values in less than 9.5 min without compromising the point‐spread function. J. Magn. Reson. Imaging 2009;30:473–480. © 2009 Wiley‐Liss, Inc.     

Automated assessment of whole‐body adipose tissue depots from continuously moving bed MRI: A feasibility study

Purpose

To present an automated algorithm for segmentation of visceral, subcutaneous, and total volumes of adipose tissue depots (VAT, SAT, TAT) from whole‐body MRI data sets and to investigate the VAT segmentation accuracy and the reproducibility of all depot assessments.

Materials and Methods

Repeated measurements were performed on 24 volunteer subjects using a 1.5 Tesla clinical MRI scanner and a three‐dimensional (3D) multi‐gradient‐echo sequence (resolution: 2.1 × 2.1 × 8 mm³, acquisition time: 5 min 15 s). Fat and water images were reconstructed, and fully automated segmentation was performed. Manual segmentation of the VAT reference was performed by an experienced operator.

Results

Strong correlation (R = 0.999) was found between the automated and manual VAT assessments. The automated results underestimated VAT with 4.7 ± 4.4%. The accuracy was 88 ± 4.5% and 7.6 ± 5.7% for true positive and false positive fractions, respectively. Coefficients of variation from the repeated measurements were: 2.32 % ± 2.61%, 2.25% ± 2.10%, and 1.01% ± 0.74% for VAT, SAT, and TAT, respectively.

Conclusion

Automated and manual VAT results correlated strongly. The assessments of all depots were highly reproducible. The acquisition and postprocessing techniques presented are likely useful in obesity related studies. J. Magn. Reson. Imaging 2009;30:185–193. © 2009 Wiley‐Liss, Inc.     

In vivo differentiation of two vessel wall layers in lower extremity peripheral vein bypass grafts: Application of high‐resolution inner‐volume black blood 3D FSE

Lower extremity peripheral vein bypass grafts (LE‐PVBG) imaged with high‐resolution black blood three‐dimensional (3D) inner‐volume (IV) fast spin echo (FSE) MRI at 1.5 Tesla possess a two‐layer appearance in T1W images while only the inner layer appears visible in the corresponding T2W images. This study quantifies this difference in six patients imaged 6 months after implantation, and attributes the difference to the T₂ relaxation rates of vessel wall tissues measured ex vivo in two specimens with histologic correlation. The visual observation of two LE‐PVBG vessel wall components imaged in vivo is confirmed to be significant (P < 0.0001), with a mean vessel wall area difference of 6.8 ± 2.7 mm² between contrasts, and a ratio of T1W to T2W vessel wall area of 1.67 ± 0.28. The difference is attributed to a significantly (P < 0.0001) shorter T₂ relaxation in the adventitia (T₂ = 52.6 ± 3.5 ms) compared with the neointima/media (T₂ = 174.7 ± 12.1 ms). Notably, adventitial tissue exhibits biexponential T₂ signal decay (P < 0.0001 vs monoexponential). Our results suggest that high‐resolution black blood 3D IV‐FSE can be useful for studying the biology of bypass graft wall maturation and pathophysiology in vivo, by enabling independent visualization of the relative remodeling of the neointima/media and adventitia. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

High‐resolution spiral imaging on a whole‐body 7T scanner with minimized image blurring

High‐resolution (～0.22 mm) images are preferably acquired on whole‐body 7T scanners to visualize minianatomic structures in human brain. They usually need long acquisition time (～12 min) in three‐dimensional scans, even with both parallel imaging and partial Fourier samplings. The combined use of both fast imaging techniques, however, leads to occasionally visible undersampling artifacts. Spiral imaging has an advantage in acquisition efficiency over rectangular sampling, but its implementations are limited due to image blurring caused by a strong off‐resonance effect at 7T. This study proposes a solution for minimizing image blurring while keeping spiral efficient. Image blurring at 7T was, first, quantitatively investigated using computer simulations and point‐spread functions. A combined use of multishot spirals and ultrashort echo time acquisitions was then employed to minimize off‐resonance‐induced image blurring. Experiments on phantoms and healthy subjects were performed on a whole‐body 7T scanner to show the performance of the proposed method. The three‐dimensional brain images of human subjects were obtained at echo time = 1.18 ms, resolution = 0.22mm (field of view = 220mm, matrix size = 1024), and in‐plane spiral shots = 128, using a home‐developed ultrashort echo time sequence (acquisition‐weighted stack of spirals). The total acquisition time for 60 partitions at pulse repetition time = 100 ms was 12.8 min without use of parallel imaging and partial Fourier sampling. The blurring in these spiral images was minimized to a level comparable to that in gradient‐echo images with rectangular acquisitions, while the spiral acquisition efficiency was maintained at eight. These images showed that spiral imaging at 7T was feasible. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Black blood dual phase turbo FLASH MR imaging of the heart

An MR imaging scheme for dark blood cardiac images acquired simultaneously in e～d diastolic and end systolic phases, in breath-hold times, is presented. The sequence consists of a magnetization preparation period followed by two segmented k-space acquisitions. Image quality was investigated with respect to different sequence parameters (optimal values are indicated in brackets): (a) echo time (TE)/repetition time (TR)/flip angle (FA) (3/6.2 msec/20°); (b) number of lines/segments in the acquisition window (11 lines/segment); (c) location of acquisition windows and inversion time; and (d) thickness of slice ?reinverted”? during preparation (1.53 times the acquisition slice thickness). The image quality of the basal slices at end systole was critically dependent on the last parameter. High quality short axis views of the heart, with good blood signal suppression, were acquired with the optimized sequence on four volunteers from apex to base at two phases in 10 breath-holds.