On the measurement of absolute cerebral blood volume (CBV) using vascular‐space‐occupancy (VASO) MRI

Recently, a vascular‐space‐occupancy (VASO) MRI technique was developed for quantitative assessment of cerebral blood volume (CBV). This method uses the T₁‐shortening effect of gadolinium diethylenetriamine pentaacetic acid (Gd‐DTPA) with imaging parameters chosen that null the precontrast blood magnetization but allow the postcontrast blood magnetization to recover to equilibrium. A key advantage of VASO CBV estimation is that it provides a straightforward procedure for converting MR signals to absolute physiologic values. However, as with other T₁‐based steady‐state approaches, several important factors need to be considered that influence the accuracy of CBV values obtained with VASO MRI. Here, the transverse relaxation (T₂/T) effect in VASO MRI was investigated using multiecho spin‐echo and gradient‐echo experiments, resulting in underestimation of CBV by 14.9% ± 1.1% and 16.0% ± 2.5% for spin echo (TE = 10 ms) and gradient echo (TE = 6 ms), respectively. In addition, the influence of contrast agent clearance was studied by acquiring multiple postcontrast VASO images at 2.2‐min intervals, which showed that the concentration of Gd‐DTPA in the first 14 min (single dose) was sufficient for the blood magnetization to fully recover to equilibrium. Finally, the effect of vascular Gd‐DTPA leakage was assessed for scalp tissue, and signal extrapolation as a function of postinjection time was demonstrated to be useful in minimizing the associated errors. Specific recommendations for VASO MRI acquisition and processing strategies are provided. Magn Reson Med, 2009. © 2008 Wiley‐Liss, Inc.     

Spin‐locked balanced steady‐state free‐precession (slSSFP)

A spin‐locked balanced steady‐state free‐precession (slSSFP) pulse sequence is described that combines a balanced gradient‐echo acquisition with an off‐resonance spin‐lock pulse for fast MRI. The transient and steady‐state magnetization trajectory was solved numerically using the Bloch equations and was shown to be similar to balanced steady‐state free‐precession (bSSFP) for a range of T₂/T₁ and flip angles, although the slSSFP steady‐state could be maintained with considerably lower radio frequency (RF) power. In both simulations and brain scans performed at 7T, slSSFP was shown to exhibit similar contrast and signal‐to‐noise ratio (SNR) efficiency to bSSFP, but with significantly lower power. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Magnetization transfer enhanced vascular‐space‐occupancy (MT‐VASO) functional MRI

Vascular‐space‐occupancy (VASO) MRI is a novel technique that uses blood signal nulling to detect blood volume alterations through changes in tissue signal. VASO has relatively low signal to noise ratio (SNR) because only 10–20% of tissue signal remain at the time of blood nulling. Here, it is shown that by adding a magnetization transfer (MT) prepulse it is possible to increase SNR either by attenuating the initial tissue magnetization when the MT pulse is placed before inversion, or, accelerating the recovery process when the pulse is applied after the inversion. To test whether the MT pulse would affect the blood nulling time in VASO, MT effects in blood were measured both ex vivo in a bovine blood phantom and in vivo in human brain. Such effects were found to be sufficiently small (< 2.5%) under a saturation power ≤ 3 μT, length = 500 ms, and frequency offset ≥40 ppm to allow use of the same nulling time. Subsequently, functional MRI experiments using MT‐VASO were performed in human visual cortex at 3 Tesla. The relative signal changes in MT‐VASO were of the same magnitude as in VASO, while the contrast to noise ratio (CNR) was enhanced by 44 ± 12% and 36 ± 11% respectively. Therefore, MT‐VASO should provide a means for increasing inherently low CNR in VASO experiments while preserving the CBV sensitivity. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Effect of inflow of fresh blood on vascular‐space‐occupancy (VASO) contrast

In vascular‐space‐occupancy (VASO)‐MRI, cerebral blood volume (CBV)‐weighted contrast is generated by applying a nonselective inversion pulse followed by imaging when blood water magnetization is zero. An uncertainty in VASO relates to the completeness of blood water nulling. Specifically, radio frequency (RF) coils produce a finite inversion volume, rendering the possibility of fresh, non‐nulled blood. Here, VASO‐functional MRI (fMRI) was performed for varying inversion volume and TR using body coil RF transmission. For thin inversion volume thickness (δ_tot < 10 mm), VASO signal changes were positive (ΔS/S = 2.1–2.6%). Signal changes were negative and varied in magnitude for intermediate inversion volumes (δ_tot = 100–300 mm), yet did not differ significantly (P > 0.05) for δ_tot > 300 mm. These data suggest that blood water is in steady state for δ_tot > 300 mm. In this appropriate range, long‐TR VASO data converged to a less negative value (ΔS/S = –1.4% ± 0.2%) than short‐TR data (ΔS/S = –2.2% ± 0.2%), implying that cerebral blood flow or transit‐state effects may influence VASO contrast at short TR. Magn Reson Med 61:473–480, 2009. © 2009 Wiley‐Liss, Inc.     

Comparison of wideband steady‐state free precession and T2‐weighted fast spin echo in spine disorder assessment at 1.5 and 3 T

Wideband steady‐state free precession (WB‐SSFP) is a modification of balanced steady‐state free precession utilizing alternating repetition times to reduce susceptibility‐induced balanced steady‐state free precession limitations, allowing its use for high‐resolution myelographic‐contrast spinal imaging. Intertissue contrast and spatial resolution of complete‐spine‐coverage 3D WB‐SSFP were compared with those of 2D T₂‐weighted fast spin echo, currently the standard for spine T₂‐imaging. Six normal subjects were imaged at 1.5 and 3 T. The signal‐to‐noise ratio efficiency (SNR per unit‐time and unit‐volume) of several tissues was measured, along with four intertissue contrast‐to‐noise ratios; nerve‐ganglia:fat, intradural‐nerves:cerebrospinal fluid, nerve‐ganglia:muscle, and muscle:fat. Patients with degenerative and traumatic spine disorders were imaged at both MRI fields to demonstrate WB‐SSFP clinical advantages and disadvantages. At 3 T, WB‐SSFP provided spinal contrast‐to‐noise ratios 3.7–5.2 times that of fast spin echo. At 1.5 T, WB‐SSFP contrast‐to‐noise ratio was 3–3.5 times that of fast spin echo, excluding a 1.7 ratio for intradural‐nerves:cerebrospinal fluid. WB‐SSFP signal‐to‐noise ratio efficiency was also higher. Three‐dimensional WB‐SSFP disadvantages relative to 2D fast spin echo are reduced edema hyperintensity, reduced muscle signal, and higher motion sensitivity. WB‐SSFP's high resolution and contrast‐to‐noise ratio improved visualization of intradural nerve bundles, foraminal nerve roots, and extradural nerve bundles, improving detection of nerve compression in radiculopathy and spinal‐stenosis. WB‐SSFP's high resolution permitted reformatting into orthogonal planes, providing distinct advantages in gauging fine spine pathology. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.     

Inflow‐based vascular‐space‐occupancy (iVASO) MRI

Vascular‐space‐occupancy (VASO) MRI, a blood nulling approach for assessing changes in cerebral blood volume (CBV), is hampered by low signal‐to‐noise ratio (SNR) because only 10–20% of tissue signal is recovered when using nonselective inversion for blood nulling. A new approach, called inflow‐VASO (iVASO), is introduced in which only blood flowing into the slice has experienced inversion, thereby keeping tissue and cerebrospinal fluid (CSF) signal in the slice maximal and reducing CSF partial volume effects. SNR increases of 198% ± 12% and 334% ± 9% (mean ± SD, n = 7) with respect to VASO were found at TR values of 5s and 2s, respectively. When using inflow approaches, data interpretation is complicated by the fact that signal changes are affected by vascular transit times. An optimal TR‐range (1.5–2.5s) was derived in which the iVASO response during activation predominantly reflects arterial/arteriolar CBV (CBV_a) changes. In this TR‐range, perfusion contributions to the signal change are negligible because arterial label has not yet undergone capillary exchange, and arterial and precapillary blood signals are nulled. For TR = 2s, the iVASO signal change upon visual stimulation corresponded to a CBV_a increase of 58% ± 7%, in agreement with arteriolar CBV changes previously reported. The onset of the hemodynamic response for iVASO occurred 1.2 ± 0.5s (n = 7) faster than for conventional VASO. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Single‐shot T1 mapping using simultaneous acquisitions of spin‐ and stimulated‐echo‐planar imaging (2D ss‐SESTEPI)

The conventional stimulated‐echo NMR sequence only measures the longitudinal component while discarding the transverse component, after tipping up the prepared magnetization. This transverse magnetization can be used to measure a spin echo, in addition to the stimulated echo. Two‐dimensional single‐shot spin‐ and stimulated‐echo‐planar imaging (ss‐SESTEPI) is an echo‐planar‐imaging‐based single‐shot imaging technique that simultaneously acquires a spin‐echo‐planar image and a stimulated‐echo‐planar image after a single radiofrequency excitation. The magnitudes of the spin‐echo‐planar image and stimulated‐echo‐planar image differ by T₁ decay and diffusion weighting for perfect 90° radiofrequency and thus can be used to rapidly measure T₁. However, the spatial variation of amplitude of radiofrequency field induces uneven splitting of the transverse magnetization for the spin‐echo‐planar image and stimulated‐echo‐planar image within the imaging field of view. Correction for amplitude of radiofrequency field inhomogeneity is therefore critical for two‐dimensional ss‐SESTEPI to be used for T₁ measurement. We developed a method for amplitude of radiofrequency field inhomogeneity correction by acquiring an additional stimulated‐echo‐planar image with minimal mixing time, calculating the difference between the spin echo and the stimulated echo and multiplying the stimulated‐echo‐planar image by the inverse functional map. Diffusion‐induced decay is corrected by measuring the average diffusivity during the prescanning. Rapid single‐shot T₁ mapping may be useful for various applications, such as dynamic T₁ mapping for real‐time estimation of the concentration of contrast agent in dynamic contrast enhancement MRI. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

T2‐weighted 3D fMRI using S2‐SSFP at 7 tesla

In this study, the sensitivity of the S₂‐steady‐state free precession (SSFP) signal for functional MRI at 7 T was investigated. In order to achieve the necessary temporal resolution, a three‐dimensional acquisition scheme with acceleration along two spatial axes was employed. Activation maps based on S₂‐steady‐state free precession data showed similar spatial localization of activation and sensitivity as spin‐echo echo‐planar imaging (SE‐EPI), but data can be acquired with substantially lower power deposition. The functional sensitivity estimated by the average z‐values was not significantly different for SE‐EPI compared to the S₂‐signal but was slightly lower for the S₂‐signal (6.74 ± 0.32 for the TR = 15 ms protocol and 7.51 ± 0.78 for the TR = 27 ms protocol) compared to SE‐EPI (7.49 ± 1.44 and 8.05 ± 1.67) using the same activated voxels, respectively. The relative signal changes in these voxels upon activation were slightly lower for SE‐EPI (2.37% ± 0.18%) compared to the TR = 15 ms S₂‐SSFP protocol (2.75% ± 0.53%) and significantly lower than the TR = 27 ms protocol (5.38% ± 1.28%), in line with simulations results. The large relative signal change for the long TR SSFP protocol can be explained by contributions from multiple coherence pathways and the low intrinsic intensity of the S₂ signal. In conclusion, whole‐brain T₂‐weighted functional MRI with negligible image distortion at 7 T is feasible using the S₂‐SSFP sequence and partially parallel imaging. Magn Reson Med 63:1015–1020, 2010. © 2010 Wiley‐Liss, Inc.     

Parallel imaging with asymmetric acceleration to reduce Gibbs artifacts and to increase signal‐to‐noise ratio of the gradient echo echo‐planar imaging sequence for functional MRI

Parallel imaging with accelerated acquisition was noted to pronounce Gibbs artifacts which appear as ripples propagated in the phase‐encoding (PE) direction near the susceptibility‐affected region in echo‐planar imaging (EPI). Using the extended EPI sequence, which collected extended readouts outside the regular data sampling time, the pronounced Gibbs artifact was analyzed and found to be caused by an increased echo shift in the pre‐echo time (T_E) of accelerated parallel imaging. This was also confirmed by theoretical derivation of the echo shift caused by the inplane susceptibility gradient in the PE direction (ISG_PE). A new EPI sequence was developed to reduce the Gibbs artifact and to restore the signal level toward that of nonaccelerated parallel imaging by asymmetrically accelerating only the post‐T_E sampling time and by using the extended EPI in the pre‐T_E. The nonaccelerated portion in the pre‐T_E used the delay for the optimum blood oxygen level dependent (BOLD) sensitivity at 3 T, maintaining the same slice coverage as the symmetrical acceleration in both pre‐T_E and post‐T_E. The increased data sampling points resulted in an increase of the signal‐to‐noise ratio (SNR). The restored signal and enhanced SNR of the proposed method were confirmed to deliver a better BOLD functional MRI (fMRI) result in the breath holding experiment. Magn Reson Med, 2012. © 2011 Wiley Periodicals, Inc.     

Optimizing signal‐to‐noise ratio of high‐resolution parallel single‐shot diffusion‐weighted echo‐planar imaging at ultrahigh field strengths

The potential signal‐to‐noise ratio (SNR) gain at ultrahigh field strengths offers the promise of higher image resolution in single‐shot diffusion‐weighted echo‐planar imaging the challenge being reduced T₂ and T₂* relaxation times and increased B₀ inhomogeneity which lead to geometric distortions and image blurring. These can be addressed using parallel imaging (PI) methods for which a greater range of feasible reduction factors has been predicted at ultrahigh field strengths—the tradeoff being an associated SNR loss. Using comprehensive simulations, the SNR of high‐resolution diffusion‐weighted echo‐planar imaging in combination with spin‐echo and stimulated‐echo acquisition is explored at 7 T and compared to 3 T. To this end, PI performance is simulated for coil arrays with a variable number of circular coil elements. Beyond that, simulations of the point spread function are performed to investigate the actual image resolution. When higher PI reduction factors are applied at 7 T to address increased image distortions, high‐resolution imaging benefits SNR‐wise only at relatively low PI reduction factors. On the contrary, it features generally higher image resolutions than at 3 T due to smaller point spread functions. The SNR simulations are confirmed by phantom experiments. Finally, high‐resolution in vivo images of a healthy volunteer are presented which demonstrate the feasibility of higher PI reduction factors at 7 T in practice. Magn Reson Med, 2012. © 2011 Wiley Periodicals, Inc.     

Flow‐independent T2‐prepared inversion recovery black‐blood MR imaging

Purpose:

To develop a magnetization preparation method to achieve robust, flow‐independent blood suppression for cardiac and vascular magnetic resonance imaging (MRI).

Materials and Methods:

T₂Prep‐IR sequence consists of a T₂ preparation followed by a nonselective adiabatic inversion pulse. T₂Prep separates the initial longitudinal magnetization of arterial wall from lumen blood. After the inversion recovery pulse the imaging acquisition is then delayed for a period that allows the blood signal to approach the zero‐crossing point. Compared to the conventional double inversion recovery (DIR) preparation, T₂Prep‐IR prepares all the spins regardless of their velocity and direction. T₂Prep‐IR was incorporated into the fast spin echo and fast gradient echo acquisition sequences and images in various planes were acquired in the carotid arteries, thoracic aorta, and heart of normal volunteers. Blood suppression and image quality were compared qualitatively between two different preparations.

Results:

For in‐plane flow carotid images, persistent flow‐related artifacts on the DIR images were removed with T₂Prep‐IR. For cardiac applications, T₂Prep‐IR provided robust blood suppression regardless of the flow direction and velocity, including the cardiac long‐axis views and the aorta that are often problematic with DIR.

Conclusion:

T₂Prep‐IR may overcome the flow dependence of DIR by providing robust flow‐independent black‐blood images. J. Magn. Reson. Imaging 2010;31:248–254. © 2009 Wiley‐Liss, Inc     

Imaging iron‐loaded mouse glioma tumors with bSSFP at 3 T

The poor prognosis for patients with high‐grade glioma is partly due to the invasion of tumor cells into surrounding brain tissue. The goal of the present work was to develop a mouse model of glioma that included the potential to track cell invasion using MRI by labeling GL261 cells with iron oxide contrast agents prior to intracranial injection. Two types of agents were compared with several labeling schemes to balance between labeling with sufficient iron to curb the dilution effect of cell division while avoiding overwhelming signal loss that could prevent adequate visualization of tumor boundaries. The balanced steady‐state free precession (bSSFP) pulse sequence was evaluated for its suitability for imaging glioma tumors and compared to T₂‐weighted two‐dimensional fast spin echo (FSE) and T₁‐weighted spoiled gradient recalled echo (SPGR) at 3 T in terms of signal‐to‐noise ratio and contrast‐to‐noise ratio efficiencies. Ultimately, a three‐dimensional bSSFP protocol consisting of a set of two images with complementary contrasts was developed, allowing excellent tumor visualization with minimal iron contrast when using pulse repetition time = 6 ms and α = 40°, and extremely high sensitivity to iron when using pulse repetition time = 22 ms and α = 20°. Quantitative histologic analysis validated that the strong signal loss seen in balanced steady state free precession pulse sequence images of iron‐loaded tumors correlated well with the presence of iron. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Hypercapnia‐induced effects on image contrast based on intermolecular double‐quantum coherences

Intermolecular double‐quantum coherences (iDQCs) are well known to be sensitive to magnetic‐field perturbations inside tissues. However, the exact relation between iDQC contrast in magnetic resonance imaging (MRI) and the underlying physiology is less well understood. To investigate parameters that influence iDQC signal changes observed during neuronal activation, carbogen‐inhalation experiments were performed to produce a pure hemodynamic response without affecting oxidative metabolism. Eight human volunteers were studied at 2.9 T using gradient‐recalled echo (GRE) and spin‐echo (SE) variants of a single‐shot sequence selecting iDQCs. Results were compared with conventional recordings of the blood oxygen level‐dependent (BOLD) effect. Maps of voxels responding to the carbogen challenge showed similar distributions for iDQC and conventional MRI after adjustment for different sensitivities. Strong diffusion weighting of iDQC sequences and transverse relaxation effects suggested quantitative suppression of intravascular signal contributions. A particular susceptibility to local gradients during the evolution period (in which iDQCs evolve at twice the Larmor frequency) plus a strong relaxation weighting during the detection period due to the use of a long echo time (for refocusing of the dipolar signal) produced iDQC signal changes up to 21.7% ± 2.5%. These results agreed quantitatively with computations based on the balloon model of BOLD‐weighted MRI without requiring further assumptions. Magn Reson Med 60:1306–1312, 2008. © 2008 Wiley‐Liss, Inc.     

SNR‐optimized phase‐sensitive dual‐acquisition turbo spin echo imaging: A fast alternative to FLAIR

Phase‐sensitive dual‐acquisition single‐slab three‐dimensional turbo spin echo imaging was recently introduced, producing high‐resolution isotropic cerebrospinal fluid attenuated brain images without long inversion recovery preparation. Despite the advantages, the weighted‐averaging‐based technique suffers from noise amplification resulting from different levels of cerebrospinal fluid signal modulations over the two acquisitions. The purpose of this work is to develop a signal‐to‐noise ratio‐optimized version of the phase‐sensitive dual‐acquisition single‐slab three‐dimensional turbo spin echo. Variable refocusing flip angles in the first acquisition are calculated using a three‐step prescribed signal evolution while those in the second acquisition are calculated using a two‐step pseudo‐steady state signal transition with a high flip‐angle pseudo‐steady state at a later portion of the echo train, balancing the levels of cerebrospinal fluid signals in both the acquisitions. Low spatial frequency signals are sampled during the high flip‐angle pseudo‐steady state to further suppress noise. Numerical simulations of the Bloch equations were performed to evaluate signal evolutions of brain tissues along the echo train and optimize imaging parameters. In vivo studies demonstrate that compared with conventional phase‐sensitive dual‐acquisition single‐slab three‐dimensional turbo spin echo, the proposed optimization yields 74% increase in apparent signal‐to‐noise ratio for gray matter and 32% decrease in imaging time. The proposed method can be a potential alternative to conventional fluid‐attenuated imaging. Magn Reson Med, 2013. © 2012 Wiley Periodicals, Inc.     

Contrast‐enhanced whole‐heart coronary MRI with bolus infusion of gadobenate dimeglumine at 1.5 T

We sought to investigate the T₁ kinetics of blood and myocardium after three infusion schemes of gadobenate dimeglumine (Gd‐BOPTA) and subsequently compared contrast‐enhanced whole‐heart coronary MRI after a bolus Gd‐BOPTA infusion with nonenhanced coronary MRI at 1.5 T. Blood and myocardium T₁ was measured in seven healthy adults, after each underwent three Gd‐BOPTA infusion schemes (bolus: 0.2 mmol/kg at 2 mL/sec, hybrid: 0.1 mmol/kg at 2 mL/sec followed by 0.1 mmol/kg at 0.1 mL/sec, and slow: 0.2 mmol/kg at 0.3 mL/sec). Fourteen additional subjects underwent contrast‐enhanced coronary MRI with an inversion‐recovery steady‐state free precession sequence after bolus Gd‐BOPTA infusion. Images were compared with nonenhanced T₂‐prepared steady‐state free precision whole‐heart coronary MRI in signal‐to‐noise ratio, contrast‐to‐noise ratio, depicted vessel length, vessel sharpness, and subjective image quality. Bolus and slow infusion schemes resulted in similar T₁ during coronary MRI, whereas the hybrid infusion method yielded higher T₁ values. A bolus infusion of Gd‐BOPTA significantly improved signal‐to‐noise ratio, contrast‐to‐noise ratio, depicted coronary artery length, and subjective image quality, when all segments were collectively compared but not when compared segment by segment. In conclusion, whole‐heart steady‐state free precision coronary MRI at 1.5 T can benefit from a bolus infusion of 0.2 mmol/kg Gd‐BOPTA. Magn Reson Med, 2011. © 2010 Wiley‐Liss, Inc.     

Contrast‐enhanced,three‐dimensional,whole‐brain,black‐blood imaging: Application to small brain metastases

Contrast‐enhanced three‐dimensional T₁‐weighted imaging based on magnetization‐prepared rapid‐gradient recalled echo is widely used for detecting small brain metastases. However, since contrast materials remain in both blood and the tumor parenchyma and thus increase the signal intensity of both regions, it is often challenging to distinguish brain tumors from blood. In this work, we develop a T₁‐weighted, black‐blood version of single‐slab three‐dimensional turbo/fast spin echo whole‐brain imaging, in which the signal intensity of the brain tumor is selectively enhanced while that of blood is suppressed. For blood suppression, variable refocusing flip angles with flow‐sensitizing gradients are employed. To avoid a signal loss resulting from the flow‐sensitizing scheme, the first refocusing flip angle is forced to 180°. Composite restore pulses at the end of refocusing pulse train are applied to achieve partial inversion recovery for the T₁‐weighted contrast. Simulations and in vivo volunteer and patient experiments are performed, demonstrating that this approach is highly efficient in detecting small brain metastases. Magn Reson Med 63:553–561, 2010. © 2010 Wiley‐Liss, Inc.     

Functional perfusion imaging using pseudocontinuous arterial spin labeling with low‐flip‐angle segmented 3D spiral readouts

Arterial spin labeling (ASL) provides quantitative and reproducible measurements of regional cerebral blood flow, and is therefore an attractive method for functional MRI. However, most existing ASL functional MRI protocols are based on either two‐dimensional (2D) multislice or 3D spin‐echo and suffer from very low image signal‐to‐noise ratio or through‐plane blurring. 3D ASL with multishot (segmented) readouts can improve the signal‐to‐noise ratio efficiency relative to 2D multislice and does not suffer from T₂‐blurring. However, segmented readouts require lower imaging flip‐angles and may increase the susceptibility to temporal signal fluctuations (e.g., due to physiology) relative to 2D multislice. In this article, we characterize the temporal signal‐to‐noise ratio of a segmented 3D spiral ASL sequence, and investigate the effects of radiofrequency phase cycling scheme and flip‐angle schedule on image properties. We show that radiofrequency‐spoiling is essential in segmented 3D spiral ASL, and that 3D ASL can improve temporal signal‐to‐noise ratio 2‐fold relative to 2D multislice when using a simple polynomial (cubic) flip‐angle schedule. Functional MRI results using the proposed optimized segmented 3D spiral ASL protocol show excellent activation in the visual cortex. Magn Reson Med, 2013. © 2012 Wiley Periodicals, Inc.     

A simple low‐SAR technique for chemical‐shift selection with high‐field spin‐echo imaging

We have discovered a simple and highly robust method for removal of chemical shift artifact in spin‐echo MR images, which simultaneously decreases the radiofrequency power deposition (specific absorption rate). The method is demonstrated in spin‐echo echo‐planar imaging brain images acquired at 7 T, with complete suppression of scalp fat signal. When excitation and refocusing pulses are sufficiently different in duration, and thus also different in the amplitude of their slice‐select gradients, a spatial mismatch is produced between the fat slices excited and refocused, with no overlap. Because no additional radiofrequency pulse is used to suppress fat, the specific absorption rate is significantly reduced compared with conventional approaches. This enables greater volume coverage per unit time, well suited for functional and diffusion studies using spin‐echo echo‐planar imaging. Moreover, the method can be generally applied to any sequence involving slice‐selective excitation and at least one slice‐selective refocusing pulse at high magnetic field strengths. The method is more efficient than gradient reversal methods and more robust against inhomogeneities of the static (polarizing) field (B₀). Magn Reson Med, 2010. © 2010 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.     

Parallel‐transmission‐enabled three‐dimensional T2‐weighted imaging of the human brain at 7 Tesla

Purpose: A promise of ultra high field MRI is to produce images of the human brain with higher spatial resolution due to an increased signal to noise ratio. Yet, the shorter radiofrequency wavelength induces an inhomogeneous distribution of the transmit magnetic field and thus challenges the applicability of MRI sequences which rely on the spin excitation homogeneity. In this work, the ability of parallel‐transmission to obtain high‐quality T₂‐weighted images of the human brain at 7 Tesla, using an original pulse design method is evaluated. Methods: Excitation and refocusing square pulses of a SPACE sequence were replaced with short nonselective transmit‐SENSE pulses individually tailored with the gradient ascent pulse engineering algorithm, adopting a k_T‐point trajectory to simultaneously mitigate B₁⁺ and ΔB₀ nonuniformities. Results: In vivo experiments showed that exploiting parallel‐transmission at 7T with the proposed methodology produces high quality T₂‐weighted whole brain images with uniform signal and contrast. Subsequent white and gray matter segmentation confirmed the expected improvements in image quality. Conclusion: This work demonstrates that the adopted formalism based on optimal control, combined with the k_T‐point method, successfully enables three‐dimensional T₂‐weighted brain imaging at 7T devoid of artifacts resulting from B₁⁺ inhomogeneity. Magn Reson Med 73:2195–2203, 2015. © 2014 Wiley Periodicals, Inc.