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.     

Rapid 3D‐imaging of phosphocreatine recovery kinetics in the human lower leg muscles with compressed sensing

The rate of phosphocreatine (PCr) resynthesis following physical exercise is an accepted index of mitochondrial oxidative metabolism and has been studied extensively with unlocalized ³¹P‐MRS methods and small surface coils. Imaging experiments using volume coils that measure several muscles simultaneously can provide new insights into the variability of muscle function in healthy and diseased states. However, they are limited by long acquisition times relative to the dynamics of PCr recovery. This work focuses on the implementation of a compressed sensing technique to accelerate imaging of PCr resynthesis following physical exercise, using a modified three‐dimensional turbo‐spin‐echo sequence and principal component analysis as sparsifying transform. The compressed sensing technique was initially validated using 2‐fold retrospective undersampling of fully sampled data from four volunteers acquired on a 7T MRI system (voxel size: 1.6 mL, temporal resolution: 24 s), which led to an accurate estimation of the mono‐exponential PCr resynthesis rate constant (mean error <6.4%). Acquisitions with prospective 2‐fold acceleration (temporal resolution: 12 s) demonstrated that three‐dimensional mapping of PCr resynthesis is possible at a temporal resolution that is sufficiently high for characterizing the recovery curve of several muscles in a single measurement. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.     

Phase‐sensitive,dual‐acquisition,single‐slab, 3D,turbo‐spin‐echo pulse sequence for simultaneous T2‐weighted and fluid‐attenuated whole‐brain imaging

Conventional T₂‐weighted turbo/fast spin echo imaging is clinically accepted as the most sensitive method to detect brain lesions but generates a high signal intensity of cerebrospinal fluid (CSF), yielding diagnostic ambiguity for lesions close to CSF. Fluid‐attenuated inversion recovery can be an alternative, selectively eliminating CSF signals. However, a long time of inversion, which is required for CSF suppression, increases imaging time substantially and thereby limits spatial resolution. The purpose of this work is to develop a phase‐sensitive, dual‐acquisition, single‐slab, three‐dimensional, turbo/fast spin echo imaging, simultaneously achieving both conventional T₂‐weighted and fluid‐attenuated inversion recovery–like high‐resolution whole‐brain images in a single pulse sequence, without an apparent increase of imaging time. Dual acquisition in each time of repetition is performed, wherein an in phase between CSF and brain tissues is achieved in the first acquisition, while an opposed phase, which is established by a sequence of a long refocusing pulse train with variable flip angles, a composite flip‐down restore pulse train, and a short time of delay, is attained in the second acquisition. A CSF‐suppressed image is then reconstructed by weighted averaging the in‐ and opposed‐phase images. Numerical simulations and in vivo experiments are performed, demonstrating that this single pulse sequence may replace both conventional T₂‐weighted imaging and fluid‐attenuated inversion recovery. Magn Reson Med 63:1422–1430, 2010. © 2010 Wiley‐Liss, Inc.     

Semi‐LASER localized dynamic 31P magnetic resonance spectroscopy in exercising muscle at ultra‐high magnetic field

Magnetic resonance spectroscopy (MRS) can benefit from increased signal‐to‐noise ratio (SNR) of high magnetic fields. In this work, the SNR gain of dynamic ³¹P MRS at 7 T was invested in temporal and spatial resolution. Using conventional slice selective excitation combined with localization by adiabatic selective refocusing (semi‐LASER) with short echo time (TE = 23 ms), phosphocreatine quantification in a 38 mL voxel inside a single exercising muscle becomes possible from single acquisitions, with SNR = 42 ± 4 in resting human medial gastrocnemius. The method was used to quantify the phosphocreatine time course during 5 min of plantar flexion exercise and recovery with a temporal resolution of 6 s (the chosen repetition time for moderate T₁ saturation). Quantification of inorganic phosphate and pH required accumulation of consecutively acquired spectra when (resting) Pi concentrations were low. The localization performance was excellent while keeping the chemical shift displacement acceptably small. The SNR and spectral line widths with and without localization were compared between 3 T and 7 T systems in phantoms and in vivo. The results demonstrate that increased sensitivity of ultra‐high field can be used to dynamically acquire metabolic information from a clearly defined region in a single exercising muscle while reaching a temporal resolution previously available with MRS in non‐localizing studies only. The method may improve the interpretation of dynamic muscle MRS data. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.     

Metabolic imaging of multiple X‐nucleus resonances

This study describes a technique for fast imaging of x‐nuclei metabolites. Due to increased sensitivity and larger chemical shift dispersion at high magnetic fields, images of multiple metabolites can be obtained simultaneously by selective excitation of their resonances with a multifrequency selective radiofrequency pulse at any desired flip angle. This aim is achieved by combining a three‐dimensional gradient echo imaging sequence with a Shinnar‐LeRoux optimized excitation pulse. A proper choice of bandwidth, imaging matrix size, and field of view allows using the chemical shift dispersion of the different resonances to completely separate their images within one large field of view. The method of fast metabolic imaging is illustrated with ¹³C measurements of a phantom containing a solution of ¹³C labeled glucose, lactate, and sodium octanoate and by dynamic measurements of the ³¹P metabolites phosphocreatine and β‐adenosine triphosphate in human femoral muscle in vivo, both at 7T. With dynamic selective ³¹P imaging of the larger part of the upper leg, phosphocreatine signal intensity changes of specific muscles can be studied simultaneously by analyzing the sum of phosphocreatine signals within arbitrarily shaped regions of interest following the muscles' contours. This concept of dynamic metabolic imaging can be applied to other organs and further expanded to other MR‐detectable nuclei and metabolites. Magn Reson Med, 2013. © 2012 Wiley Periodicals, Inc.     

两种MRCP成像技术的临床应用价值分析

目的:探讨两种MRCP成像技术的临床应用价值。方法:对150例受检者同时进行两种MRCP成像方法的扫描:一是二维单次激发快速自旋回波、厚层多角度成像,以胆总管为定位中心屏气完成扫描;另一成像方法为快速自旋回波三维薄层扫描,采用呼吸门控方式完成。根据图像的空间分辨率,对比度,呼吸运动伪影状况以及背景干扰因素等,对两种MRCP图像分别评级。χ2检验两种扫描方法图像间的差异性。结果:二维成像方法获得的图像中Ⅰ级、Ⅱ级合计142例,Ⅲ级8例;三维图像中,Ⅰ级、Ⅱ级合计125例,Ⅲ级25例。χ2检验结果:χ2=9.84,P=0.002。结论:两种MRCP方法的侧重点不同,在临床实际应用中同时进行上述两种方法的MRCP成像是必要的。     

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.     

Echo planar correlated spectroscopic imaging: Implementation and pilot evaluation in human calf in vivo

Exploiting the speed benefits of echo‐planar imaging (EPI), the echo‐planar spectroscopic imaging (EPSI) sequence facilitates recording of one spectral and two to three spatial dimensions faster than the conventional magnetic resonance spectroscopic imaging (MRSI). A novel four dimensional (4D) echo‐planar correlated spectroscopic imaging (EP‐COSI) was implemented on a whole body 3 T MRI scanner combining two spectral with two spatial encodings. Similar to EPSI, the EP‐COSI sequence used a bipolar spatial read‐out train facilitating simultaneous spatial and spectral encoding, and the conventional phase and spectral encodings for the other spatial and indirect spectral dimensions, respectively. Multiple 2D correlated spectroscopy (COSY) spectra were recorded over the spatially resolved volume of interest (VOI) localized by a train of three slice‐selective radiofrequency (RF) pulses (90°–180°–90°). After the initial optimization using phantom solutions, the EP‐COSI data were recorded from the lower leg of eight healthy volunteers including one endurance trained volunteer. Pilot results showed acceptable spatial and spectral quality achievable using the EP‐COSI sequence. There was a detectable separation of cross peaks arising from the skeletal muscle intramyocellular lipids (IMCLs) and extramyocellular lipids (EMCLs) saturated and unsaturated pools. Residual dipolar interaction between the N‐methylene and N‐methyl protons of creatine/phosphocreatine (Cr/PCr) was also observed in the tibialis anterior region. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Assessment of anterior cruciate ligament reconstruction using 3D ultrashort echo‐time MR imaging

This work demonstrates the potential of ultrashort TE (UTE) imaging for visualizing graft material and fixation elements after surgical repair of soft tissue trauma such as ligament or meniscal injury. Three asymptomatic patients with anterior cruciate ligament (ACL) reconstruction using different graft fixation methods were imaged at 1.5T using a 3D UTE sequence. Conventional multislice turbo spin‐echo (TSE) measurements were performed for comparison. 3D UTE imaging yields high signal from tendon graft material at isotropic spatial resolution, thus facilitating direct positive contrast graft visualization. Furthermore, metal and biopolymer graft fixation elements are clearly depicted due to the high contrast between the signal‐void implants and the graft material. Thus, the ability of UTE MRI to visualize short‐T₂ tissues such as tendons, ligaments, or tendon grafts can provide additional information about the status of the graft and its fixation in the situation after cruciate ligament repair. UTE MRI can therefore potentially support diagnosis when problems occur or persist after surgical procedures involving short‐T₂ tissues and implants. J. Magn. Reson. Imaging 2009;29:443–448. © 2009 Wiley‐Liss, Inc.     

Fast‐spin‐echo imaging of inner fields‐of‐view with 2D‐selective RF excitations

Purpose:

To demonstrate the feasibility of two‐dimensional selective radio frequency (2DRF) excitations for fast‐spin‐echo imaging of inner fields‐of‐view (FOVs) in order to shorten acquisitions times, decrease RF energy deposition, and reduce image blurring.

Materials and Methods:

Fast‐spin‐echo images (in‐plane resolution 1.0 × 1.0 mm² or 0.5 × 1.0 mm²) of inner FOVs (40 mm, 16 mm oversampling) were obtained in phantoms and healthy volunteers on a 3 T whole‐body MR system using blipped‐planar 2DRF excitations.

Results:

Positioning the unwanted side excitations in the blind spot between the image section and the slice stack to measure yields minimum 2DRF pulse durations (about 6 msec) that are compatible with typical echo spacings of fast‐spin‐echo acquisitions. For the inner FOVs, the number of echoes and refocusing RF pulses is considerably reduced which compared to a full FOV (182 mm) reduces the RF energy deposition by about a factor of three and shortens the acquisition time, e.g., from 39 seconds to 12 seconds for a turbo factor of 15 or from 900 msec to 280 msec for a single‐shot acquisition, respectively. Furthermore, image blurring occurring for high turbo factors as in single‐shot acquisitions is considerably reduced yielding effectively higher in‐plane resolutions.

Conclusion:

Inner‐FOV acquisitions using 2DRF excitations may help to shorten acquisitions times, ameliorate image blurring, and reduce specific absorption rate (SAR) limitations of fast‐spin‐echo (FSE) imaging, in particular at higher static magnetic fields. J. Magn. Reson. Imaging 2010;31:1530–1537. © 2010 Wiley‐Liss, Inc.     

Reduction of B1 sensitivity in selective single‐slab 3d turbo spin echo imaging with very long echo trains

Single‐slab 3D turbo/fast spin echo (SE) imaging with very long echo trains was recently introduced with slab selection using a highly selective excitation pulse and short, nonselective refocusing pulses with variable flip angles for high imaging efficiency. This technique, however, is vulnerable to image degradation in the presence of spatially varying B₁ amplitudes. In this work we develop a B₁ inhomogeneity‐reduced version of single‐slab 3D turbo/fast SE imaging based on the hypothesis that it is critical to achieve spatially uniform excitation. Slab selection was performed using composite adiabatic selective excitation wherein magnetization is tipped into the transverse plane by a nonselective adiabatic‐half‐passage pulse and then slab is selected by a pair of selective adiabatic‐full‐passage pulses. Simulations and experiments were performed to evaluate the proposed technique and demonstrated that this approach is a simple and efficient way to reduce B₁ sensitivity in single‐slab 3D turbo/fast SE imaging with very long echo trains. Magn Reson Med, 2009. © 2009 Wiley‐Liss, 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.     

Optimized three‐dimensional fast‐spin‐echo MRI

Spin‐echo‐based acquisitions are the workhorse of clinical MRI because they provide a variety of useful image contrasts and are resistant to image artifacts from radio‐frequency or static field inhomogeneity. Three‐dimensional (3D) acquisitions provide datasets that can be retrospectively reformatted for viewing in freely selectable orientations, and are thus advantageous for evaluating the complex anatomy associated with many clinical applications of MRI. Historically, however, 3D spin‐echo‐based acquisitions have not played a significant role in clinical MRI due to unacceptably long acquisition times or image artifacts associated with details of the acquisition method. Recently, optimized forms of 3D fast/turbo spin‐echo imaging have become available from several MR‐equipment manufacturers (for example, CUBE [GE], SPACE [Siemens], and VISTA [Philips]). Through specific design strategies and optimization, including short non–spatially selective radio‐frequency pulses to significantly shorten the echo spacing and variable flip angles for the refocusing radio‐frequency pulses to suppress blurring or considerably lengthen the useable duration of the spin‐echo train, these techniques permit single‐slab 3D imaging of sizeable volumes in clinically acceptable acquisition times. These optimized fast/turbo spin‐echo pulse sequences provide a robust and flexible approach for 3D spin‐echo‐based imaging with a broad range of clinical applications. J. Magn. Reson. Imaging 2014;39:745–767. © 2014 Wiley Periodicals, Inc .     

Combining two‐dimensional spatially selective RF excitation,parallel imaging,and UNFOLD for accelerated MR thermometry imaging

MR thermometry can be a very challenging application, as good resolution may be needed along spatial, temporal, and temperature axes. Given that the heated foci produced during thermal therapies are typically much smaller than the anatomy being imaged, much of the imaged field‐of‐view is not actually being heated and may not require temperature monitoring. In this work, many‐fold improvements were obtained in terms of temporal resolution and/or 3D spatial coverage by sacrificing some of the in‐plane spatial coverage. To do so, three fast‐imaging approaches were jointly implemented with a spoiled gradient echo sequence: (1) two‐dimensional spatially selective RF excitation, (2) unaliasing by Fourier encoding the overlaps using the temporal dimension (UNFOLD), and (3) parallel imaging. The sequence was tested during experiments with focused ultrasound heating in ex vivo tissue and a tissue‐mimicking phantom. Temperature maps were estimated from phase‐difference images based on the water proton resonance frequency shift. Results were compared to those obtained from a spoiled gradient echo sequence sequence, using a t‐test. Temporal resolution was increased by 24‐fold, with temperature uncertainty less than 1°C, while maintaining accurate temperature measurements (mean difference between measurements, as observed in gel = 0.1°C ± 0.6; R = 0.98; P > 0.05). Magn Reson Med 66:112–122, 2011. © 2011 Wiley‐Liss, Inc.     

Carotid arterial wall MRI at 3T using 3D variable‐flip‐angle turbo spin‐echo (TSE) with flow‐sensitive dephasing (FSD)

Purpose:

To evaluate the effectiveness of flow‐sensitive dephasing (FSD) magnetization preparation in improving blood signal suppression of three‐dimensional (3D) turbo spin‐echo (TSE) sequence (SPACE) for isotropic high‐spatial‐resolution carotid arterial wall imaging at 3T.

Materials and Methods:

The FSD‐prepared SPACE sequence (FSD‐SPACE) was implemented by adding two identical FSD gradient pulses right before and after the first refocusing 180°‐pulse of the SPACE sequence in all three orthogonal directions. Nine healthy volunteers were imaged at 3T with SPACE, FSD‐SPACE, and multislice T2‐weighted 2D TSE coupled with saturation band (SB‐TSE). Apparent carotid wall‐lumen contrast‐to‐noise ratio (aCNR_w‐l) and apparent lumen area (aLA) at the locations with residual‐blood (rb) signal shown on SPACE images were compared between SPACE and FSD‐SPACE. Carotid aCNR_w‐l and lumen (LA) and wall area (WA) measured from FSD‐SPACE were compared to those measured from SB‐TSE.

Results:

Plaque‐mimicking flow artifacts identified in seven carotids on SPACE images were eliminated on FSD‐SPACE images. The FSD preparation resulted in slightly reduced aCNR_w‐l (P = 0.025), but significantly improved aCNR between the wall and rb regions (P < 0.001) and larger aLA (P < 0.001). Compared to SB‐TSE, FSD‐SPACE offered comparable aCNR_w‐l with much higher spatial resolution, shorter imaging time, and larger artery coverage. The LA and WA measurements from the two techniques were in good agreement based on intraclasss correlation coefficient (0.988 and 0.949, respectively; P < 0.001) and Bland‐Altman analyses.

Conclusion:

FSD‐SPACE is a time‐efficient 3D imaging technique for carotid arterial wall with superior spatial resolution and blood signal suppression. J. Magn. Reson. Imaging 2010;31:645–654. © 2010 Wiley‐Liss, Inc.     

Multiecho coarse voxel acquisition for neurofeedback fMRI

“Real‐time” functional magnetic resonance imaging is starting to be used in neurofeedback applications, enabling individuals to regulate their brain activity for therapeutic purposes. These applications use two‐dimensional multislice echo planar or spiral readouts to image the entire brain volume, often with a much smaller region of interest within the brain monitored for feedback purposes. Given that such brain activity should be sampled rapidly, it is worthwhile considering alternative functional magnetic resonance imaging pulse sequences that trade spatial resolution for temporal resolution. We developed a prototype sequence localizing a column of magnetization by outer volume saturation, from which densely sampled transverse relaxation time decays are obtained at coarse voxel locations using an asymmetric gradient echo train. For 5 × 20 × 20 mm3 voxels, 256 echoes are sampled at ～1 msec and then combined in weighted summation to increase functional magnetic resonance imaging signal contrast. This multiecho coarse voxel pulse sequence is shown experimentally at 1.5 T to provide the same signal contrast to noise ratio as obtained by spiral imaging for a primary motor cortex region of interest, but with potential for enhanced temporal resolution. A neurofeedback experiment also illustrates measurement and calculation of functional magnetic resonance imaging signals within 1 sec, emphasizing the future potential of the approach. Magn Reson Med, 2011. © 2010 Wiley‐Liss, Inc.     

3D compressed sensing for highly accelerated hyperpolarized 13C MRSI with in vivo applications to transgenic mouse models of cancer

High polarization of nuclear spins in liquid state through hyperpolarized technology utilizing dynamic nuclear polarization has enabled the direct monitoring of ¹³C metabolites in vivo at a high signal‐to‐noise ratio. Acquisition time limitations due to T₁ decay of the hyperpolarized signal require accelerated imaging methods, such as compressed sensing, for optimal speed and spatial coverage. In this paper, the design and testing of a new echo‐planar ¹³C three‐dimensional magnetic resonance spectroscopic imaging (MRSI) compressed sensing sequence is presented. The sequence provides up to a factor of 7.53 in acceleration with minimal reconstruction artifacts. The key to the design is employing x and y gradient blips during a fly‐back readout to pseudorandomly undersample k_f‐k_x‐k_y space. The design was validated in simulations and phantom experiments where the limits of undersampling and the effects of noise on the compressed sensing nonlinear reconstruction were tested. Finally, this new pulse sequence was applied in vivo in preclinical studies involving transgenic prostate cancer and transgenic liver cancer murine models to obtain much higher spatial and temporal resolution than possible with conventional echo‐planar spectroscopic imaging methods. Magn Reson Med, 2010. © 2009 Wiley‐Liss, Inc.     

2D axial moving table acquisitions with dynamic slice adaptation

A method for axial multi‐slice imaging during continuous table motion has been developed and implemented on a clinical scanner. Multiple axial slice packages are acquired consecutively and combined to cover an extended longitudinal FOV. To account for the table motion during the acquisition, the RF pulse frequencies are continuously updated according to the actual table velocity and slice position. Different strategies for the spatial‐temporal acquisition sequence with extended FOV are proposed. They cover different regimes of scan requirements regarding table velocity, used scan range, and slice resolution. The method is easy to implement and compatible with most kinds of sequences. The robustness of the proposed approach has been tested in phantom studies and healthy volunteers using T1‐, T2‐, and STIR‐weighted multi‐slice techniques that are based on gradient and turbo spin echo sequences and compared to a stationary approach usually used in clinical routine. The method provides artifact free gradient echo based images during continuous table motion, while for turbo spin echo sequences limitations in choosing table translations occur due to gradient non‐linearity effects. Magn Reson Med, 2006. © 2006 Wiley‐Liss, Inc.     

Coronary artery wall imaging: initial experience at 3 Tesla

Purpose

To assess the feasibility of black‐blood turbo spin‐echo imaging of the left anterior descending coronary artery wall at 3 Tesla under free‐breathing and breath‐hold conditions.

Materials and Methods

Proton density‐weighted black‐blood turbo spin‐echo imaging of the left anterior descending coronary artery was performed on 15 volunteers on a 3 T whole body scanner with an eight channel phased array coil. Volunteers were imaged during free‐breathing (with navigators, N = 5), or with breath‐hold (N = 5), or both (N = 2). Imaging was not possible in three volunteers due to either gradient or radiofrequency (RF) coupling with the electrocardiogram (ECG). Images were analyzed to determine coronary artery wall thickness, wall area, lumen diameter, and lumen area. Signal‐to‐noise and contrast‐to‐noise ratios were calculated.

Results

Coronary artery wall thickness, wall area, lumen diameter, and lumen area measurements were consistent with previous magnetic resonance (MR) measurements of the coronary wall at 1.5 Tesla.

Conclusion

Coronary wall imaging using free‐breathing and breath‐hold two‐dimensional black‐blood TSE is feasible at 3 T. Further improvement in resolution and image quality is required to detect and characterize coronary plaque. J. Magn. Reson. Imaging 2005;21:128–132. © 2005 Wiley‐Liss, Inc.

     

In vivo high‐resolution imaging of the injured rat spinal cord using a 3.0T clinical MR scanner

Purpose

To investigate the feasibility of obtaining high‐resolution MR images for the detection of pathological changes occurring in the injured rat spinal cord with a routine clinical 3.0T imaging system.

Materials and Methods

Adult female Fischer 344 rats received thoracic spine contusion injuries. In vivo MR imaging was performed on days 1 and 43 postinjury with a clinical head 3.0T imaging system equipped with a dedicated small animal 4‐channel phased array spine surface coil using T2‐weighted turbo spin‐echo and T1‐weighted spin‐echo sequences.

Results

The acquired images provide good spatial resolution allowing reliable gray/white matter differentiation in the intact spinal cord as well as detection of hemorrhage, edema, and cystic degenerative changes in the injured rat spinal cord as confirmed by correlation with structural alterations in histological sections.

Conclusion

Results from the present study demonstrate that a routine clinical MR imaging system can be employed for noninvasive analysis of pathological changes occurring in the injured rat spinal cord and thus might represent a more broadly available, powerful tool to monitor the effects of experimental therapeutic interventions in vivo. J. Magn. Reson. Imaging 2009;29:725–730. © 2009 Wiley‐Liss, Inc.