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  • Articles  (391)
  • PAPER CURRENT  (391)
  • 2010-2014  (391)
  • 2012  (391)
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  • PAPER CURRENT  (391)
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  • 2010-2014  (391)
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  • 1
    Publication Date: 2012-12-28
    Description: Purpose: To develop and evaluate variable-density spiral first-pass perfusion pulse sequences for improved efficiency and off-resonance performance and to demonstrate the utility of an apodizing density compensation function (DCF) to improve signal-to-noise ratio (SNR) and reduce dark-rim artifact caused by cardiac motion and Gibbs Ringing. Methods: Three variable density spiral trajectories were designed, simulated, and evaluated in 18 normal subjects, and in eight patients with cardiac pathology on a 1.5T scanner. Results: By using a DCF, which intentionally apodizes the k -space data, the sidelobe amplitude of the theoretical point spread function (PSF) is reduced by 68%, with only a 13% increase in the full-width at half-maximum of the main-lobe when compared with the same data corrected with a conventional variable-density DCF, and has an 8% higher resolution than a uniform density spiral with the same number of interleaves and readout duration. Furthermore, this strategy results in a greater than 60% increase in measured SNR when compared with the same variable-density spiral data corrected with a conventional DCF ( P 〈 0.01). Perfusion defects could be clearly visualized with minimal off-resonance and dark-rim artifacts. Conclusion: Variable-density spiral pulse sequences using an apodized DCF produce high-quality first-pass perfusion images with minimal dark-rim and off-resonance artifacts, high SNR and contrast-to-noise ratio, and good delineation of resting perfusion abnormalities. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
    Print ISSN: 0740-3194
    Electronic ISSN: 1522-2594
    Topics: Medicine
    Published by Wiley-Blackwell
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  • 2
    Publication Date: 2012-12-28
    Description: Purpose: To develop an arrhythmia-insensitive rapid (AIR) cardiac T 1 mapping pulse sequence for quantification of diffuse fibrosis. Methods: An arrhythmia-insensitive cardiac T 1 mapping pulse sequence was developed based on saturation recovery T 1 weighting, which is inherently insensitive to heart rate and rhythm, and two single-shot balanced steady-state free precession image acquisitions with centric k-space ordering, where T 1 calculation is inherently insensitive to T 2 effects. Its performance against conventional cardiac T 1 mapping based on inversion recovery (i.e., MOLLI) is compared. Phantom experiments ( T 1 ranging from 535 to 2123 ms) were performed with heart rate and rhythm simulated at 60 and 120 beats per minute (bpm) and arrhythmia using an external triggering device. Ten human subjects and 17 large animals were scanned precontrast and 5, 10, and 15 min after contrast agent administration. Results: Compared with the reference T 1 mapping, AIR yielded lower normalized root-mean-square error than MOLLI (8% vs. 3%, respectively, at 60 bpm, 28% vs. 3%, respectively, at 120 bpm, and 22% vs. 3%, respectively, at arrhythmia). In vivo studies showed that T 1 measurements made by MOLLI and AIR were strongly correlated ( r = 0.99) but in poor agreement (mean difference = 161.8 ms, upper and lower 95% limits of agreements = 347.5 ms and −24.0 ms). Conclusion: Our AIR pulse sequence may be clinically useful for assessment of diffuse myocardial fibrosis in patients. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Electronic ISSN: 1522-2594
    Topics: Medicine
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  • 3
    Publication Date: 2012-12-28
    Description: Purpose : Quantification of cerebral blood flow can be accomplished by model-free arterial spin labeling using the quantitative STAR labeling of arterial regions (QUASAR) sequence. The required deconvolution is normally based on block-circulant singular value decomposition (cSVD)/oscillation SVD (oSVD), an algorithm associated with nonphysiological residue functions and potential effects of arterial dispersion. The aim of this work was to amend this by implementing nonlinear stochastic regularization (NSR) deconvolution, previously used to retrieve realistic residue functions in dynamic susceptibility contrast MRI. Methods: To characterize the residue function in model-free arterial spin labeling, and possibly to improve absolute cerebral blood flow quantification, NSR was applied to deconvolution of QUASAR data. For comparison, SVD-based deconvolution was also employed. Residue function characteristics and cerebral blood flow values from 10 volunteers were obtained. Simulations were performed to support the in vivo results. Results: NSR was able to resolve realistic residue functions in contrast to the SVD-based methods. Mean cerebral blood flow estimates in gray matter were 36.6 ± 2.6, 28.6 ± 3.3, 40.9 ± 3.6, and 42.9 ± 3.9 mL/100 g/min for cSVD, oSVD, NSR, and NSR with correction for arterial dispersion, respectively. In simulations, the NSR-based perfusion estimates showed better accuracy than the SVD-based approaches. Conclusion: Perfusion quantification by model-free arterial spin labeling is evidently dependent on the selected deconvolution method, and NSR is a feasible alternative to SVD-based methods. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Topics: Medicine
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  • 4
    Publication Date: 2012-12-28
    Description: In small rodent myocardial perfusion studies, the most widely used method is based on Look-Locker measurements of the magnetization recovery after FAIR preparation, which bears limitations regarding acquisition efficiency due to the pulsed arterial spin labeling nature of the sequence. To improve efficiency, this two-article set proposes a new steady-pulsed arterial spin labeling scheme using a cine readout incorporating one tagging pulse per heart cycle. In this part, we derive a theoretical description of the magnetization time evolution in such a scheme. The combination of steady-pulsed labeling and cine readout drives tissue magnetization into a stationary regime that explicitly depends on perfusion. In comparison with dedicated experiments on the mouse heart, the model is discussed and validated for perfusion quantification. The model predicts that in this regime, signal is independent of irregular dynamics occurring during acquisition, such as heart rate variations or arterial input function. Optimization of the sequence offers the possibility to increase the signal to noise ratio by efficient signal averaging. The sensitivity of this new method is shown to be more than three times larger than previously used techniques. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Topics: Medicine
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  • 5
    Publication Date: 2012-12-28
    Description: Purpose: To present and validate a new method that formalizes a direct link between k-space and wavelet domains to apply separate undersampling and reconstruction for high- and low-spatial-frequency k-space data. Theory and Methods: High- and low-spatial-frequency regions are defined in k-space based on the separation of wavelet subbands, and the conventional compressed sensing problem is transformed into one of localized k-space estimation. To better exploit wavelet-domain sparsity, compressed sensing can be used for high-spatial-frequency regions, whereas parallel imaging can be used for low-spatial-frequency regions. Fourier undersampling is also customized to better accommodate each reconstruction method: random undersampling for compressed sensing and regular undersampling for parallel imaging. Results: Examples using the proposed method demonstrate successful reconstruction of both low-spatial-frequency content and fine structures in high-resolution three-dimensional breast imaging with a net acceleration of 11–12. Conclusion: The proposed method improves the reconstruction accuracy of high-spatial-frequency signal content and avoids incoherent artifacts in low-spatial-frequency regions. This new formulation also reduces the reconstruction time due to the smaller problem size. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Electronic ISSN: 1522-2594
    Topics: Medicine
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  • 6
    Publication Date: 2012-12-28
    Description: Purpose: Pregnancy complications such as preeclampsia and fetal growth restriction are sometimes thought to be caused by placental abnormalities associated with reduced oxygenation. Oxygen-enhanced MRI ( R 1 contrast) and BOLD MRI ( R 2 * contrast) have the potential to noninvasively investigate this oxygen environment at a range of gestational ages. Methods: Scanning was carried out at 1.5 T under maternal air and oxygen breathing in a single placental slice in 14 healthy pregnant subjects of gestational ages 21–37 weeks. We report R 1 changes using a respiratory-triggered inversion recovery-turbo spin-echo sequence, which is sensitive to changes in PO 2 , and R 2 * changes using a breathhold multiple gradient-recalled echo sequence sensitive to changes in oxygen saturation. Results: Significant R 1 increases ( P 〈 0.005, paired t-test) and R 2 * decreases ( P 〈 0.0001, paired t-test) between air and oxygen breathing were demonstrated. Δ R 1 decreased with gestational age ( P 〈 0.0005, r = −0.835, Pearson correlation test). No significant effect of gestational age on R 2 * change was observed. Conclusion: The results demonstrate the feasibility of non-invasive investigation of placental oxygenation using MRI and the sensitivity of R 1 oxygen-enhanced MRI to gestational age. The techniques have the potential to provide unique noninvasive biomarkers in compromised pregnancies. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Topics: Medicine
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  • 7
    Publication Date: 2012-12-28
    Description: Purpose: In this study, we sought to investigate the feasibility of turbo fast three-dimensional (3D) black-blood imaging by combining a 3D motion-sensitizing driven equilibrium rapid gradient echo sequence with compressed sensing. Methods: A pseudo-centric phase encoding order was developed for compressed sensing-3D motion-sensitizing driven equilibrium rapid gradient echo to suppress flow signal in undersampled 3D k-space. Nine healthy volunteers were recruited for this study. Signal-to-tissue ratio, contrast-to-tissue ratio (CTR) and CTR efficiency (CTR eff ) between fully sampled and undersampled images were calculated and compared in seven subjects. Moreover, isotropic high resolution images using different compressed sensing acceleration factors were evaluated in two other subjects. Results: Wall-lumen signal-to-tissue ratio or CTR were comparable between the undersampled and the fully sampled images, while significant improvement of CTR eff was achieved in the undersampled images. At an isotropic high spatial resolution of 0.7 × 0.7 × 0.7 mm 3 , all undersampled images exhibited similar level of the flow suppression efficiency and the capability of delineating outer vessel wall boundary and lumen-wall interface, when compared with the fully sampled images. Conclusion: The proposed turbo fast compressed sensing 3D black-blood imaging technique improves scan efficiency without sacrificing flow suppression efficiency and vessel wall image quality. It could be a valuable tool for rapid 3D vessel wall imaging. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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  • 8
    Publication Date: 2012-12-28
    Description: MRI is a method of choice for assessing anatomical structures or angiogenesis-related parameters noninvasively during tumor progression. Typically, tumor tissue displays a high degree of heterogeneity that can be evaluated using pattern analysis (PA), which comprises shape and texture analysis. This work aims at implementing PA methods to study angiogenesis in a murine tumor model and testing its sensitivity with regard to detecting changes elicited by administration of a drug. Twelve balb/c-nude mice were injected subcutaneously with 10 6 C51 cells (colon carcinoma). A first group ( N = 6) of animals was treated with dimethyloxalylglycine, a drug known to stabilize hypoxia-inducible-factor-α, which among other functions, is involved in angiogenesis. The second group ( N = 6) was treated with saline. MRI experiments assessing tumor blood volume and permeability-maps ( K trans ) were performed immediately before and 6 days after drug treatment. Data have been analyzed using standard histogram analysis and PA. Standard histogram analysis did not reveal any difference between the two groups, neither before nor after the treatment. In contrast, PA revealed significant differences between drug and placebo treated mice in the texture of the TBV and K trans maps after drug treatment, but not with regard to tumors shapes. The results indicated that in view of the heterogeneity of tumor tissue, standard histogram analysis appears insensitive in picking-up differences in response to treatment, while PA appears to be particularly sensitive to changes in texture. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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  • 9
    Publication Date: 2012-12-28
    Description: Purpose: Partial volume (PV) effects are caused by limited spatial resolution and significantly affect cerebral blood flow investigations with arterial spin labeling. Therefore, accurate PV correction (PVC) procedures are required. PVC is commonly based on PV maps obtained from segmented high-resolution T 1 -weighted images. Segmentation of these images is error-prone, and it can be difficult to coregister these images accurately with the single-shot ASL images such as those created by echo-planar imaging (EPI). In this paper, an alternative method for PV map generation is proposed. Methods: The Look-Locker EPI (LL-EPI) acquisition is used for analyzing the T 1 -recovery curve and for subsequent PV map generation. The new method was evaluated in five healthy volunteers (mean age 30 ± 3.7 years). Results: By applying a linear regression method for PVC, a 12% decrease in regression error was reached with the new method. Conclusion: PV maps extraction from LL-EPI is a viable, possibly superior alternative to the standard approach based on segmentation of high-resolution T 1 -weighted images. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Topics: Medicine
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  • 10
    Publication Date: 2012-12-28
    Description: Diffusion-weighted images of the liver exhibit signal dropout from cardiac and respiratory motion, particularly in the left lobe. These artifacts cause bias and variance in derived parameters that quantify intravoxel incoherent motion. Many models of diffusion have been proposed, but few separate attenuation from diffusion or perfusion from that of bulk motion. The error model proposed here (Beta*LogNormal) is intended to accomplish that separation by modeling stochastic attenuation from bulk motion as multiplication by a Beta-distributed random variate. Maximum likelihood estimation with this error model can be used to derive intravoxel incoherent motion parameters separate from signal dropout, and does not require a priori specification of parameters to do so. Liver intravoxel incoherent motion parameters were derived for six healthy subjects under this error model and compared with least-squares estimates. Least-squares estimates exhibited bias due to cardiac and respiratory gating and due to location within the liver. Bias from these factors was significantly reduced under the Beta*LogNormal model, as was within-organ parameter variance. Similar effects were appreciable in diffusivity maps in two patients with focal liver lesions. These results suggest that, relative to least-squares estimation, the Beta*LogNormal model accomplishes the intended reduction of bias and variance from bulk motion in liver diffusion imaging. Magn Reson Med, 2012. © 2012 Wiley Periodicals, Inc.
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    Topics: Medicine
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