Permeability dependence study of the focused ultrasound‐induced blood–brain barrier opening at distinct pressures and microbubble diameters using DCE‐MRI

Blood–brain barrier opening using focused ultrasound and microbubbles has been experimentally established as a noninvasive and localized brain drug delivery technique. In this study, the permeability of the opening is assessed in the murine hippocampus after the application of focused ultrasound at three different acoustic pressures and microbubble sizes. Using dynamic contrast‐enhanced MRI, the transfer rates were estimated, yielding permeability maps and quantitative K_trans values for a predefined region of interest. The volume of blood–brain barrier opening according to the K_trans maps was proportional to both the pressure and the microbubble diameter. A K_trans plateau of ～0.05 min^?1 was reached at higher pressures (0.45 and 0.60 MPa) for the larger sized bubbles (4–5 and 6–8 μm), which was on the same order as the K_trans of the epicranial muscle (no barrier). Smaller bubbles (1–2 μm) yielded significantly lower permeability values. A small percentage (7.5%) of mice showed signs of damage under histological examination, but no correlation with permeability was established. The assessment of the blood–brain barrier permeability properties and their dependence on both the pressure and the microbubble diameter suggests that K_trans maps may constitute an in vivo tool for the quantification of the efficacy of the focused ultrasound‐induced blood–brain barrier opening. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.     

Enhancement of gas‐filled microbubble R2* by iron oxide nanoparticles for MRI

Gas‐filled microbubbles have the potential to become a unique intravascular MR contrast agent due to their magnetic susceptibility effect, biocompatibility, and localized manipulation via ultrasound cavitation. However, microbubble susceptibility effect is relatively weak when compared with other intravascular MR susceptibility contrast agents. In this study, enhancement of microbubble susceptibility effect by entrapping monocrystalline iron oxide nanoparticles (MIONs) into polymeric microbubbles was investigated at 7 T in vitro. Apparent T₂ enhancement (ΔR₂*) induced by microbubbles was measured to be 79.2 ± 17.5 sec^?1 and 301.2 ± 16.8 sec^?1 for MION‐free and MION‐entrapped polymeric microbubbles at 5% volume fraction, respectively. ΔR₂* and apparent transverse relaxivities (r₂*) for MION‐entrapped polymeric microbubbles and MION‐entrapped solid microspheres (without gas core) were also compared, showing the synergistic effect of the gas core with MIONs. This is the first experimental demonstration of microbubble susceptibility enhancement for MRI application. This study indicates that gas‐filled polymeric microbubble susceptibility effect can be substantially increased by incorporating iron oxide nanoparticles into microbubble shells. With such an approach, microbubbles can potentially be visualized with higher sensitivity and lower concentrations by MRI. Magn Reson Med, 2010. © 2009 Wiley‐Liss, Inc.     

Contrast‐enhanced in vivo magnetic resonance microscopy of the mouse brain enabled by noninvasive opening of the blood‐brain barrier with ultrasound

The use of contrast agents for neuroimaging is limited by the blood‐brain barrier (BBB), which restricts entry into the brain. To administer imaging agents to the brain of rats, intracarotid infusions of hypertonic mannitol have been used to open the BBB. However, this technically challenging approach is invasive, opens only a limited region of the BBB, and is difficult to extend to mice. In this work, the BBB was opened in mice, using unfocused ultrasound combined with an injection of microbubbles. This technique has several notable features: it (a) can be performed transcranially in mice; (b) takes only 3 min and uses only commercially available components; (c) opens the BBB throughout the brain; (d) causes no observed histologic damage or changes in behavior (with peak‐negative acoustic pressures of 0.36 MPa); and (e) allows recovery of the BBB within 4 h. Using this technique, Gadopentetate Dimeglumine (Gd‐DTPA) was administered to the mouse brain parenchyma, thereby shortening T₁ and enabling the acquisition of high‐resolution (52 × 52 × 100 micrometers³) images in 51 min in vivo. By enabling the administration of both existing anatomic contrast agents and the newer molecular/sensing contrast agents, this technique may be useful for the study of mouse models of neurologic function and pathology with MRI. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Quantitative measurement of blood‐brain barrier permeability in human using dynamic contrast‐enhanced MRI with fast T1 mapping

Breakdown of the blood‐brain barrier (BBB), occurring in many neurological diseases, has been difficult to measure noninvasively in humans. Dynamic contrast‐enhanced magnetic resonance imaging measures BBB permeability. However, important technical challenges remain and normative data from healthy humans is lacking. We report the implementation of a method for measuring BBB permeability, originally developed in animals, to estimate BBB permeability in both healthy subjects and patients with white matter pathology. Fast T₁ mapping was used to measure the leakage of contrast agent Gadolinium diethylene triamine pentaacetic acid (Gd‐DTPA) from plasma into brain. A quarter of the standard Gd‐DTPA dose for dynamic contrast‐enhanced magnetic resonance imaging was found to give both sufficient contrast‐to‐noise and high T₁ sensitivity. The Patlak graphical approach was used to calculate the permeability from changes in 1/T₁. Permeability constants were compared with cerebrospinal fluid albumin index. The upper limit of the 95% confidence interval for white matter BBB permeability for normal subjects was 3 × 10^?4 L/g min. MRI measurements correlated strongly with levels of cerebrospinal fluid albumin in those subjects undergoing lumbar puncture. Dynamic contrast‐enhanced magnetic resonance imaging with low dose Gd‐DTPA and fast T₁ imaging is a sensitive method to measure subtle differences in BBB permeability in humans and may have advantages over techniques based purely on the measurement of pixel contrast changes. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Quantitative 19F imaging of nmol‐level F‐nucleotides/‐sides from 5‐FU with T2 mapping in mice at 9.4T

A unique acquisition method is proposed for quantitative, high‐sensitivity ¹⁹F MR spectroscopic imaging for the study of drug distribution aiming at nmol‐level metabolite information in mice. The use of fast spin echo (FSE) at 9.4T allowed us to obtain whole‐body images with minimal effect of magnetic susceptibility and to acquire several metabolite signals simultaneously by the method of interleaved multifrequency selection. Modified 2‐shot FSE was designed for simultaneous, high‐sensitivity ¹⁹F imaging and T₂ mapping. A time course study including all the main metabolites at 10‐minute resolution was attained with an oral dose of 1–2 mmol 5‐fluorouracil (5‐FU) (130–260 mg)/kg in mice. With acquisition parameters optimized for in vivo T₂ of 40 ms, images of F‐nucleotides/‐sides, effective anabolites of the anticancer drug 5‐FU, were obtained at the level of 200 nmol in the tumor for all the mice studied with a linear correlation (R = 0.96) between image intensity and the quantity determined in the excised tissue. The method exhibits potential capability of molecular imaging with a variety of ¹⁹F‐labeled compounds and drug evaluation. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Ischemia‐reperfusion injury in rat skeletal muscle assessed with T2‐weighted and dynamic contrast‐enhanced MRI

Pressure ulcers are localized areas of soft tissue breakdown due to mechanical loading. Susceptible individuals are subjected to pressure relief strategies to prevent long loading periods. Therefore, ischemia‐reperfusion injury may play an important role in the etiology of pressure ulcers. To investigate the inter‐relation between postischemic perfusion and changes in skeletal muscle integrity, the hindlimbs of Brown Norway rats were subjected to 4‐h ischemia followed by 2‐h reperfusion. Dynamic contrast‐enhanced MRI was used to examine perfusion, and changes in skeletal muscle integrity were monitored with T₂‐weighted MRI. The dynamic contrast‐enhanced MRI data showed a heterogeneous postischemic profile in the hindlimb, consisting of areas with increased contrast enhancement (14–76% of the hindlimb) and regions with no‐reflow (5–77%). For T₂, a gradual increase in the complete leg was observed during the 4‐h ischemic period (from 34 to 41 msec). During the reperfusion phase, a heterogeneous distribution of T₂ was observed. Areas with increased contrast enhancement were associated with a decrease in T₂ (to 38 msec) toward preischemic levels, whereas no‐reflow areas exhibited a further increase in T₂ (to 42 msec). These results show that reperfusion after prolonged ischemia may not be complete, thereby continuing the ischemic condition and aggravating tissue damage. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.     

Combined use of T2‐weighted MRI and T1‐weighted dynamic contrast–enhanced MRI in the automated analysis of breast lesions

A multiparametric computer‐aided diagnosis scheme that combines information from T₁‐weighted dynamic contrast–enhanced (DCE)‐MRI and T₂‐weighted MRI was investigated using a database of 110 malignant and 86 benign breast lesions. Automatic lesion segmentation was performed, and three categories of lesion features (geometric, T₁‐weighted DCE, and T₂‐weighted) were automatically extracted. Stepwise feature selection was performed considering only geometric features, only T₁‐weighted DCE features, only T₂‐weighted features, and all features. Features were merged with Bayesian artificial neural networks, and diagnostic performance was evaluated by ROC analysis. With leave‐one‐lesion‐out cross‐validation, an area under the ROC curve value of 0.77 ± 0.03 was achieved with T₂‐weighted‐only features, indicating high diagnostic value of information in T₂‐weighted images. Area under the ROC curve values of 0.79 ± 0.03 and 0.80 ± 0.03 were obtained for geometric‐only features and T₁‐weighted DCE‐only features, respectively. When all features were considered, an area under the ROC curve value of 0.85 ± 0.03 was achieved. We observed P values of 0.006, 0.023, and 0.0014 between the geometric‐only, T₁‐weighted DCE‐only, and T₂‐weighted‐only features and all features conditions, respectively. When ranked, the P values satisfied the Holm–Bonferroni multiple‐comparison test; thus, the improvement of multiparametric computer‐aided diagnosis was statistically significant. A computer‐aided diagnosis scheme that combines information from T₁‐weighted DCE and T₂‐weighted MRI may be advantageous over conventional T₁‐weighted DCE‐MRI computer‐aided diagnosis. Magn Reson Med, 2011. © 2011 Wiley‐Liss, Inc.     

FASCINATE: A pulse sequence for simultaneous acquisition of T2‐weighted and fluid‐attenuated images

A pulse sequence that enables simultaneous acquisition of T₂‐weighted and fluid‐attenuated images is presented. This sequence is referred to as FASCINATE (Fluid‐Attenuated Scan Combined with Interleaved Non‐ATtEnuation). In this new technique, the inversion pulse of conventional fast fluid‐attenuated inversion recovery (FLAIR) is replaced with a fast spin echo (FSE) acquisition that has an additional 180(y)–90(x) pulse train for driven inversion. By using appropriate scan parameters, the first part of the sequence provides T₂‐weighted images and the second part provides fluid‐attenuated images, thus allowing simultaneous acquisition in a single scan time comparable to that of fast FLAIR. FASCINATE was compared with conventional scanning techniques using a normal volunteer and a patient. A signal simulation was also conducted. In the human study, both T₂‐weighted and fluid‐attenuated images from FASCINATE showed the same image quality as conventional images, suggesting the potential for this technique to replace the combination of fast FLAIR and T₂‐weighted FSE for scan time reduction. Magn Reson Med 51:205–211, 2004. © 2003 Wiley‐Liss, Inc.     

Reduction of residual dipolar interaction in cartilage by spin‐lock technique

The influence of radiofrequency (RF) spin‐lock pulse on the laminar appearance of articular cartilage in MR images was investigated. Spin‐lock MRI experiments were performed on bovine cartilage plugs on a 4.7 Tesla small‐bore MRI scanner, and on human knee cartilage in vivo on a 1.5 Tesla clinical scanner. When the normal to the surface of cartilage was parallel to B₀, a typical laminar appearence was exhibited in T₂‐weighted images of cartilage plugs, but was absent in T_1ρ‐weighted images of the same plugs. At the “magic angle” orientation (when the normal to the surface of cartilage was 54.7° with respect to B₀), neither the T₂ nor the T_1ρ images demonstrated laminae. At the same time, T_1ρ values were greater than T₂ at both orientations throughout the cartilage. T_1ρ dispersion (i.e., the dependence of the relaxation rate on the spin‐lock frequency ω₁) was observed, which reached a steady‐state value of close to 2 kHz in both parallel and magic‐angle orientations. These results suggest that residual dipolar interaction from motionally‐restricted water and relaxation processes, such as chemical exchange, contribute to T_1ρ dispersion in cartilage. Further, one can reduce the laminar appearance in human articular cartilage by applying spin‐lock RF pulses, which may lead to a more accurate diagnosis of degenerative changes in cartilage. Magn Reson Med 52:1103–1109, 2004. © 2004 Wiley‐Liss, 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.     

High‐resolution magnetic resonance colonography and dynamic contrast‐enhanced magnetic resonance imaging in a murine model of colitis

Inflammatory bowel disease, including ulcerative colitis, is characterized by persistent or recurrent inflammation and can progress to colon cancer. Colitis is difficult to detect and monitor noninvasively. The goal of this work was to develop a preclinical imaging method for evaluating colitis. Herein, we report improved MRI methods for detecting and characterizing colitis noninvasively in mice, using high‐resolution in vivo MR images and dynamic contrast‐enhanced MRI studies, which were confirmed by histologic studies in a murine model of colitis. C57Bl6/J male mice were treated with 2.5% dextran sulfate sodium in their drinking water for 5 days to induce colitis. MR images were acquired using a 9.4‐T Bruker scanner from 5–25 days following dextran sulfate sodium treatment. In dynamic contrast‐enhanced MRI studies, Gd uptake (K^trans) and its distribution (v_e) were measured in muscle and normal and inflamed colons after administering Gd‐diethyltriaminepentaacetic acid (Gd‐DTPA). T₂‐weighted MR images distinguished normal colon from diffusely thickened colonic wall occurring in colitis (P <0.0005) and correlated with histologic features. Values of K^trans and v_e obtained from dynamic contrast‐enhanced MRI were also significantly different in inflamed colons compared to normal colon (P < 0.0005). The results demonstrate that both T₂‐weighted anatomic imaging and quantitative analysis of dynamic contrast‐enhanced MRI data can successfully distinguish colitis from normal colon in mice. Magn Reson Med 63:922–929, 2010. © 2010 Wiley‐Liss, Inc.     

Ultrashort TE imaging with off‐resonance saturation contrast (UTE‐OSC)

Short T₂ species such as the Achilles tendon and cortical bone cannot be imaged with conventional MR sequences. They have a much broader absorption lineshape than long T₂ species, therefore they are more sensitive to an appropriately placed off‐resonance irradiation. In this work, a technique termed ultrashort TE (UTE) with off‐resonance saturation contrast (UTE‐OSC) is proposed to image short T₂ species. A high power saturation pulse was placed +1 to +2 kHz off the water peak to preferentially saturate signals from short T₂ species, leaving long T₂ water and fat signals largely unaffected. The subtraction of UTE images with and without an off‐resonance saturation pulse effectively suppresses long T₂ water and fat signals, creating high contrast for short T₂ species. The UTE‐OSC technique was validated on a phantom, and applied to bone samples and healthy volunteers on a clinical 3T scanner. High‐contrast images of the Achilles tendon and cortical bone were generated with a high contrast‐to‐noise ratio (CNR) of the order of 12 to 20 between short T₂ and long T₂ species within a total scan time of 4 to 10 min. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Experimental protocol for activation‐induced manganese‐enhanced MRI (AIM‐MRI) based on quantitative determination of Mn content in rat brain by fast T1 mapping

In activation‐induced manganese‐enhanced MRI (AIM‐MRI) experiments, differential accumulation of Mn in activated and silent brain areas is generally assessed using T₁‐weighted images and quantified by the enhancement of signal intensity (SI), calculated with reference to SI before Mn administration or to SI of brain regions unaffected by the specific stimulus. However, SI enhancement can be unreliable when animals are removed from and reinserted into the magnet. We have developed an experimental protocol based on repeated intraperitoneal (i.p.) injections of Mn, quantitative determination of T₁, and coregistration of images to a rat brain atlas that allows absolute quantification of Mn concentration in selected brain areas. Results showed that interanimal variability of postcontrast T₁ values was very low (compared to the experimental error in T₁ determinations) allowing detection of differential regional Mn uptake in stimulated and unstimulated animals. In addition we have determined in vivo relaxivity of Mn in brain tissue and its frequency dependence. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Fat‐water separated delayed hyperenhanced myocardial infarct imaging

Fat deposition associated with myocardial infarction (MI) has been reported as a commonly occurring phenomenon. Magnetic resonance imaging (MRI) has the ability to efficiently detect MI using T₁‐sensitive contrast‐enhanced sequences and fat via its resonant frequency shift. In this work, the feasibility of fat‐water separation applied to the conventional delayed hyperenhanced (DHE) MI imaging technique is demonstrated. A three‐point Dixon acquisition and reconstruction was combined with an inversion recovery gradient‐echo pulse sequence. This allowed fat‐water separation along with T₁ sensitive imaging after injection of a gadolinium contrast agent. The technique is demonstrated in phantom experiments and three subjects with chronic MI. Areas of infarction were well defined as conventional hyperenhancement in water images. In two cases, fatty deposition was detected in fat images and confirmed by precontrast opposed‐phase imaging. Magn Reson Med 60:503–509, 2008. © 2008 Wiley‐Liss, Inc.     

Association between contrast‐enhanced MR images and blood–brain barrier disruption following transcranial focused ultrasound

Purpose:

To investigate the correlation between the contrast‐enhanced magnetic resonance imaging (MRI) signal and the duration of blood–brain barrier (BBB) disruption induced by focused ultrasound (FUS).

Materials and Methods:

FUS was applied to 45 rat brains in the presence of microbubbles, and these rats were scanned on a 3T MRI system at several timepoints. The rat brains were then studied using contrast‐enhanced spin echo T1‐weighted images. At the same time, BBB disruption was evaluated based on Evans blue (EB) extravasation. The relationship between the normalized signal intensity change of the MRI and EB extravasation was analyzed by least‐squares linear regression and the calculation of correlation coefficients.

Results:

When MRI enhancement was quantitatively evaluated by EB extravasation, a strong correlation between the normalized signal intensity change of the MRI and EB extravasation was identified during BBB disruption after sonication. However, the correlation coefficient decreased as BBB closure occurred after sonication ended.

Conclusion:

The contrast‐enhanced MRI signal can potentially be used to evaluate the amount of chemotherapeutic agents entering the targeted tissue, but the accuracy of the assessment will be affected by the time interval since sonication. J. Magn. Reson. Imaging 2010;32:593–599. © 2010 Wiley‐Liss, Inc.     

A short‐breath‐hold technique for lung pO2 mapping with 3He MRI

A pulse‐sequence strategy was developed for generating regional maps of alveolar oxygen partial pressure (pO₂) in a single 6‐sec breath hold, for use in human subjects with impaired lung function. Like previously described methods, pO₂ values are obtained by measuring the oxygen‐induced T₁ relaxation of inhaled hyperpolarized ³He. Unlike other methods, only two ³He images are acquired: one with reverse‐centric and the other with centric phase‐encoding order. This phase‐encoding arrangement minimizes the effects of regional flip‐angle variations, so that an accurate map of instantaneous pO₂ can be calculated from two images acquired a few seconds apart. By combining this phase‐encoding strategy with variable flip angles, the vast majority of the hyperpolarized magnetization goes directly into the T₁ measurement, minimizing noise in the resulting pO₂ map. The short‐breath‐hold pulse sequence was tested in phantoms containing known O₂ concentrations. The mean difference between measured and prepared pO₂ values was 1 mm Hg. The method was also tested in four healthy volunteers and three lung‐transplant patients. Maps of healthy subjects were largely uniform, whereas focal regions of abnormal pO₂ were observed in diseased subjects. Mean pO₂ values varied with inhaled O₂ concentration. Mean pO₂ was consistent with normal steady‐state values in subjects who inhaled ³He diluted only with room air. Magn Reson Med 63:127–136, 2010. © 2009 Wiley‐Liss, Inc.     

3D flow‐independent peripheral vessel wall imaging using T2‐prepared phase‐sensitive inversion‐recovery steady‐state free precession

Purpose:

To develop a 3D flow‐independent peripheral vessel wall imaging method using T₂‐prepared phase‐sensitive inversion‐recovery (T₂PSIR) steady‐state free precession (SSFP).

Materials and Methods:

A 3D T₂‐prepared and nonselective inversion‐recovery SSFP sequence was designed to achieve flow‐independent blood suppression for vessel wall imaging based on T₁ and T₂ properties of the vessel wall and blood. To maximize image contrast and reduce its dependence on the inversion time (TI), phase‐sensitive reconstruction was used to restore the true signal difference between vessel wall and blood. The feasibility of this technique for peripheral artery wall imaging was tested in 13 healthy subjects. Image signal‐to‐noise ratio (SNR), wall/lumen contrast‐to‐noise ratio (CNR), and scan efficiency were compared between this technique and conventional 2D double inversion recovery – turbo spin echo (DIR‐TSE) in eight subjects.

Results:

3D T₂PSIR SSFP provided more efficient data acquisition (32 slices and 64 mm in 4 minutes, 7.5 seconds per slice) than 2D DIR‐TSE (2–3 minutes per slice). SNR of the vessel wall and CNR between vessel wall and lumen were significantly increased as compared to those of DIR‐TSE (P < 0.001). Vessel wall and lumen areas of the two techniques are strongly correlated (intraclass correlation coefficients: 0.975 and 0.937, respectively; P < 0.001 for both). The lumen area of T₂PSIR SSFP is slightly larger than that of DIR‐TSE (P = 0.008). The difference in vessel wall area between the two techniques is not statistically significant.

Conclusion:

T₂PSIR SSFP is a promising technique for peripheral vessel wall imaging. It provides excellent blood signal suppression and vessel wall/lumen contrast. It can cover a 3D volume efficiently and is flow‐ and TI‐independent. J. Magn. Reson. Imaging 2010;32:399–408. © 2010 Wiley‐Liss, Inc.     

Transverse relaxation time (T2) mapping in the brain with off‐resonance correction using phase‐cycled steady‐state free precession imaging

Purpose

To investigate a new approach for more completely accounting for off‐resonance affects in the DESPOT2 (driven equilibrium single pulse observation of T₂) mapping technique.

Materials and Methods

The DESPOT2 method derives T₂ information from fully balanced steady‐state free precession (bSSFP) images acquired over multiple flip angles. Off‐resonance affects, which present as bands of altered signal intensity throughout the bSSFP images, results in erroneous T₂ values in the corresponding calculated maps. Radiofrequency (RF) phase‐cycling, in which the phase of the RF pulse is incremented along the pulse train, offers a potential method for eliminating these artifacts. In this work we present a general method, referred to as DESPOT2, with full modeling (DESPOT2‐FM), for deriving T₂, as well as off‐resonance frequency, from dual flip angle bSSFP data acquired with two RF phase increments.

Results

The method is demonstrated in vivo through the acquisition of whole‐brain, 1 mm³ isotropic T₂ maps at 3T and shown to provide near artifact‐free maps, even in areas with steep susceptibility‐induced gradients.

Conclusion

DESPOT2‐FM offers an efficient method for acquiring high spatial resolution, whole‐brain T₂ maps at 3T with high precision and free of artifact. J. Magn. Reson. Imaging 2009;30:411–417. © 2009 Wiley‐Liss, Inc.     

Comparison of amyloid plaque contrast generated by T2‐weighted,T‐weighted,and susceptibility‐weighted imaging methods in transgenic mouse models of Alzheimer's disease

One of the hallmark pathologies of Alzheimer's disease (AD) is amyloid plaque deposition. Plaques appear hypointense on T₂‐weighted and T‐weighted MR images probably due to the presence of endogenous iron, but no quantitative comparison of various imaging techniques has been reported. We estimated the T₁, T₂, T, and proton density values of cortical plaques and normal cortical tissue and analyzed the plaque contrast generated by a collection of T₂‐weighted, T‐weighted, and susceptibility‐weighted imaging (SWI) methods in ex vivo transgenic mouse specimens. The proton density and T₁ values were similar for both cortical plaques and normal cortical tissue. The T₂ and T values were similar in cortical plaques, which indicates that the iron content of cortical plaques may not be as large as previously thought. Ex vivo plaque contrast was increased compared to a previously reported spin‐echo sequence by summing multiple echoes and by performing SWI; however, gradient echo and SWI were found to be impractical for in vivo imaging due to susceptibility interface–related signal loss in the cortex. Magn Reson Med, 2009. © 2009 Wiley‐Liss, Inc.     

Myocardial fat quantification in humans: Evaluation by two‐point water‐fat imaging and localized proton spectroscopy

Proton MR spectroscopy (¹H‐MRS) has been used for in vivo quantification of intracellular triglycerides within the sarcolemma. The purpose of this study was to assess whether breath‐hold dual‐echo in‐ and out‐of‐phase MRI at 3.0 T can quantify the fat content of the myocardium. Biases, including T₁, T*₂, and noise, that confound the calculation of the fat fraction were carefully corrected. Thirty‐four of 46 participants had both MRI and MRS data. The fat fractions from MRI showed a strong correlation with fat fractions from MRS (r = 0.78; P < 0.05). The mean myocardial fat fraction for all 34 subjects was 0.7 ± 0.5% (range: 0.11–3%) assessed with MRS and 1.04 ± 0.4% (range: 0.32–2.44%) assessed with in‐ and out‐of‐phase MRI (P < 0.05). Scanning times were less than 15 sec for Dixon imaging, plus an additional minute for the acquisition used for T*₂ calculation, and 15‐20 min for MRS. The average postprocessing time for MRS was 3 min and 5 min for MRI including T*₂ measurement. We conclude that the dual echo method provides a rapid means to detect and quantifying myocardial fat content in vivo. Correction/adjustment for field inhomogeneity using three or more echoes seems crucial for the dual echo approach. Magn Reson Med 63:892–901, 2010. © 2010 Wiley‐Liss, Inc.