Conventional Pulse Sequences Research Articles

Rapid three-dimensional quantification of high-intensity plaques from coronary atherosclerosis T1-weighted characterization to predict periprocedural myocardial injury

BackgroundHigh-intensity plaque (HIP) on magnetic resonance imaging (MRI) has been documented as a powerful predictor of periprocedural myocardial injury (PMI) following percutaneous coronary intervention (PCI). Despite the recent proposal of three-dimensional HIP quantification to enhance the predictive capability, the conventional pulse sequence, which necessitates the separate acquisition of anatomical reference images, hinders accurate three-dimensional segmentation along the coronary vasculature. Coronary atherosclerosis T1-weighted characterization (CATCH) enables the simultaneous acquisition of inherently coregistered dark-blood plaque and bright-blood coronary artery images. We aimed to develop a novel HIP quantification approach using CATCH and to ascertain its superior predictive performance compared to the conventional two-dimensional assessment based on plaque-to-myocardium signal intensity ratio (PMR). MethodsIn this prospective study, CATCH MRI was conducted before elective stent implantation in 137 lesions from 125 patients. On CATCH images, dedicated software automatically generated tubular three-dimensional volumes of interest on the dark-blood plaque images along the coronary vasculature, based on the precisely matched bright-blood coronary artery images, and subsequently computed PMR and HIP volume (HIPvol). Specifically, HIPvol was calculated as the volume of voxels with signal intensity exceeding that of the myocardium, weighted by their respective signal intensities. PMI was defined as post-PCI cardiac troponin-T > 5 × the upper reference limit. ResultsThe entire analysis process was completed within 3 min per lesion. PMI occurred in 44 lesions. Based on the receiver operating characteristic curve analysis, HIPvol outperformed PMR for predicting PMI (C-statistics, 0.870 [95% CI, 0.805–0.936] vs. 0.787 [95% CI, 0.706–0.868]; p = 0.001). This result was primarily driven by the higher sensitivity HIPvol offered: 0.886 (95% CI, 0.754–0.962) vs. 0.750 for PMR (95% CI, 0.597–0.868; p = 0.034). Multivariable analysis identified HIPvol as an independent predictor of PMI (odds ratio, 1.15 per 10-μL increase; 95% CI, 1.01–1.30, p = 0.035). ConclusionsOur semi-automated method of analyzing coronary plaque using CATCH MRI provided rapid HIP quantification. Three-dimensional assessment using this approach had a better ability to predict PMI than conventional two-dimensional assessment.

DEVELOPMENT AND APPLICATION OF R1RHO DISPERSION IMAGING OF AGING MUSCLE IN AN ANIMAL MODEL

Abstract Compelling evidence from animal studies demonstrates that microvascular impairment contributes to the etiologies of several age-related chronic diseases, including sarcopenia. For example, capillary hemodynamic profiles are altered in old F344 rat spinotrapezius muscle compared with those of younger counterparts. However, a validated non-invasive measure of microvasculature geometry and structure has not yet been developed. Recently, it has been shown that R1ρ dispersion imaging at weak locking field frequencies (FSL) provides a unique way of characterizing microvessel size and density. Moreover, previous R1ρ images were acquired at strong FSL (≥500Hz) and used to measure the age-related differences linked to macromolecular deposition, such as collagen in the extracellular matrix. Here, we aimed to develop a non-invasive 3D volume R1ρ dispersion imaging method at weak FSLs (< 300Hz), to quantify microvasculature changes in skeletal muscle. We successfully implemented the protocol and applied it to the lower leg of five F334 female rats at age 15 mo. The whole lower leg of each rat was also imaged using conventional multislice T1-FLASH, Diffusion-weighted, and T2-MGE pulse sequences. We found that R1p value measured in calf muscles decreased from 46.92Hz to 41.63Hz by increasing FSL from 5Hz to 240Hz, which we suggest derives from the effects of rephasing some of the signal losses that arise from diffusion in intrinsic magnetic field gradients generated from microvessels. Future direction of this ongoing study will be to compare these results with data collected from young female rats at age 6 months and further validation using ex-vivo histology.

Optimized three-dimensional ultrashort echo time: Magnetic resonance fingerprinting for myelin tissue fraction mapping.

Quantitative assessment of brain myelination has gained attention for both research and diagnosis of neurological diseases. However, conventional pulse sequences cannot directly acquire the myelin-proton signals due to its extremely short T2 and T2* values. To obtain the myelin-proton signals, dedicated short T2 acquisition techniques, such as ultrashort echo time (UTE) imaging, have been introduced. However, it remains challenging to isolate the myelin-proton signals from tissues with longer T2. In this article, we extended our previous two-dimensional ultrashort echo time magnetic resonance fingerprinting (UTE-MRF) with dual-echo acquisition to three dimensional (3D). Given a relatively low proton density (PD) of myelin-proton, we utilized Cramér-Rao Lower Bound to encode myelin-proton with the maximal SNR efficiency for optimizing the MR fingerprinting design, in order to improve the sensitivity of the sequence to myelin-proton. In addition, with a second echo of approximately 3ms, myelin-water component can be also captured. A myelin-tissue (myelin-proton and myelin-water) fraction mapping can be thus calculated. The optimized 3D UTE-MRF with dual-echo acquisition is tested in simulations, physical phantom and in vivo studies of both healthy subjects and multiple sclerosis patients. The results suggest that the rapidly decayed myelin-proton and myelin-water signal can be depicted with UTE signals of our method at clinically relevant resolution (1.8 mm isotropic) in 15 min. With its good sensitivity to myelin loss in multiple sclerosis patients demonstrated, our method for the whole brain myelin-tissue fraction mapping in clinical friendly scan time has the potential for routine clinical imaging.

Zero Echo Time vs. T1-Weighted MRI for Assessment of Cortical and Medullary Bone Morphology Abnormalities Using CT as the Reference Standard.

Conventional MR pulse sequences result in poor signal from low T2 cortical bone because the minimum achievable echo time is limited. A sequence resulting in improved bone contrast is desirable. To evaluate the image quality and diagnostic performance of grayscale inversion zero echo time imaging (GI-ZTE) and grayscale inversion T1-weighted imaging (GI-T1WI) compared with computed tomography (CT). Prospective. A total of 50 patients with musculoskeletal tumors or tumor-like diseases of the lower extremities having MRI and CT studies. GI-T1WI and GI-ZTE sequences at 1.5T. Assessed cortical and medullary bone morphology abnormalities using CT as the reference standard. Three radiologists scored the images quality and recorded nine metrics to assess the diagnostic performance. Differences in image quality were calculated using the Wilcoxon signed-rank test. The intraclass correlation coefficient (ICC) was used to analyze the agreement of quantitative lesion parameters between CT and MR sequences, as well as the interobserver reliability. A P value <0.05 was considered statistically significant. Image quality score was significantly higher for CT images than GI-TIWI images. Except for radiologist 3 [4(0) vs 4 (1)], there was no significant difference in scores between CT and GI-ZTE [radiologist 1: 4 (0) vs 4 (0), P=0.133; radiologist 2: 4 (0) vs 4 (0), P=0.085]. There was good-excellent agreement between both MR sequences and CT for size, lesion number, location, sclerotic rim, expanded shell, destruction pattern, and matrix mineralization for all radiologists (ICC: 0.636-1.000). The consistency of periosteal reaction and penetration of the cortex was fair to good (0.481-0.729) between GI-T1WI and CT and good to excellent between GI-ZTE and CT (0.682-0.852). GI-ZTE images had superior intermodality agreement with CT images and allowed visualization of more cortical bone detail than GI-T1WI images. 1. Stage 2.

Contrast-enhanced ultrasound to detect active bleeding

Non-compressible internal hemorrhage (NCIH) is the most common cause of death in acute non-penetrating trauma. NCIH management requires accurate hematoma localization and evaluation for ongoing bleeding for risk stratification. The current standard point-of-care diagnostic tool, the focused assessment with sonography for trauma (FAST), detects free fluid in body cavities with conventional B-mode imaging. The FAST does not assess whether bleeding is ongoing, at which location(s), and to what extent. Here, we propose contrast-enhanced ultrasound (CEUS) techniques to better identify, localize, and quantify hemorrhage. We designed and fabricated a custom hemorrhage-mimicking phantom, comprising a perforated vessel and cavity to simulate active bleeding. Lumason contrast agents (UCAs) were introduced at clinically relevant concentrations (3.5×108 bubbles/ml). Conventional and contrast pulse sequence images were captured, and post-processed with bubble localization techniques (SVD clutter filter and bubble localization). The results showed contrast pulse sequences enabled a 2.2-fold increase in the number of microbubbles detected compared with conventional CEUS imaging, over a range of flow rates, concentrations, and localization processing parameters. Additionally, particle velocimetry enabled mapping of dynamic flow within the simulated bleeding site. Our findings indicate that CEUS combined with advanced image processing may enhance visualization of hemodynamics and improve non-invasive, real-time detection of active bleeding.

Atomic-Scale Quantum Sensing of Ensembles of Guest Molecules in a Metal-Organic Framework with Intrinsic Electron Spin Centers.

One of the exciting applications of electron-spin-based quantum sensing is the detection of distant nuclear spins of external molecular species. Here, we explore the application of a metal-organic framework (MOF) material as a host matrix for sensing spin centers. As a sensor, we employ inherent Cu2+ ions in the structure of a Zn-doped HKUST-1 framework. As a target molecular species, we use butane gas that exhibits no specific chemical reactivity toward the inner surface of HKUST-1 and is thus randomly distributed inside the MOF pore network. By employing a conventional double-resonance pulse sequence, we can effectively detect the coupling of the distant 1H nuclear spins of butane to the electron spin of the sensor and gain atomic-scale insight into their spatial distribution. Thus, our proof-of-the-concept experiment demonstrates that MOFs, the materials featuring extremely large surface area and great tunability, are perfectly suited as a key element for emerging magnetic quantum sensing solutions.

High-resolution systolic T1 mapping with compressed sensing for the evaluation of the right ventricle: a phantom and volunteer study.

To investigate the usefulness of high-resolution systolic T1 mapping using compressed sensing for right ventricular (RV) evaluation. Phantoms and normal volunteers were scanned at 3T by using a high-resolution (HR) modified look-locker inversion recovery (MOLLI) pulse sequence and a conventional MOLLI pulse sequence. The T1 values of the left ventricular (LV) and RV myocardium and blood pool were measured for each sequence. T1 values of HR-MOLLI and MOLLI sequences were compared in the LV myocardium, blood pool, and RV myocardium. The T1 values of HR-MOLLI and MOLLI showed good agreement in both phantoms and the LV myocardium and blood pool of volunteers. However, there was a significant difference between HR-MOLLI and MOLLI in the RV myocardium (1258 ± 52ms vs. 1327 ± 73ms; P = 0.0005). No significant difference was observed between the T1 value of RV and that of LV (1217 ± 32ms) in HR-MOLLI, whereas the T1 value of RV was significantly higher than that of LV in MOLLI (P < 0.0001). The interclass correlation coefficients of intraobserver variabilities from HR-MOLLI and MOLLI were 0.919 and 0.804, respectively, and the interobserver variabilities from HR-MOLLI and MOLLI were 0.838 and 0.848, respectively. Assessment of RV myocardium by using HR systolic T1 mapping was superior to the conventional MOLLI sequence in terms of accuracy and reproducibility.

Technical Update on MR Neurography.

Imaging evaluation of peripheral nerves (PNs) is challenging. Magnetic resonance imaging (MRI) and ultrasonography are the modalities of choice in the imaging assessment of PNs. Both conventional MRI pulse sequences and advanced techniques have important roles. Routine MR sequences are the workhorse, with the main goal to provide superb anatomical definition and identify focal or diffuse nerve T2 signal abnormalities. Selective techniques, such as three-dimensional (3D) cranial nerve imaging (CRANI) or 3D NerveVIEW, allow for a more detailed evaluation of normal and pathologic states. These conventional pulse sequences have a limited role in the comprehensive assessment of pathophysiologic and ultrastructural abnormalities of PNs. Advanced functional MR neurography sequences, such as diffusion tensor imaging tractography or T2 mapping, provide useful and robust quantitative parameters that can be useful in the assessment of PNs on a microscopic level. This article offers an overview of various technical parameters, pulse sequences, and protocols available in the imaging of PNs and provides tips on avoiding potential pitfalls.

Reducing “slice cross-talk” effect in metamaterial assisted fast spin-echo MRI

Imaging of subtle changes in hand structures is challenged by the limited image quality, especially at 1.5 T. Reduction of specific absorption rate in metamaterial-assisted 1.5 T MRI provides an opportunity to utilize efficient pulse sequences and to improve the quality of acquired images. This work is devoted to the assessment of potential improvements of slice selectivity and reducing a ”slice cross-talk” artifact, using fast spin-echo (FSE) pulse sequence together with a metamaterial-based coil. The slice selection in conventional T1-weighted FSE wrist imaging pulse sequences was modeled using a ”Bloch Equations Simulator”. Two types of pulses were compared: apodized SINC pulses (reference) common for clinical FSE, and optimized selective Shinnar–Le Roux (SLR) pulses constructed in the MATPULSE program. Regular and SLR-based FSE pulse sequences were tested in a phantom experiment with different gaps between slices to investigate the “slice cross-talk” artifact presence. Combining the utilization of the metamaterial-based coil with an SLR-based FSE provided 28 times lower energy deposition in a duty cycle, as compared to the regular FSE with a conventional transmit coil. When the slice gap was decreased from 100% to 0%, the “slice cross-talk” effect reduced the signal intensity by 16%-18% in the SLR-based FSE and by 23%-32% for the regular FSE. The use of SLR pulses together with the metamaterial-based coil allowed to reduce the ”slice cross-talk” effect in contiguous FSE, while still being within the safe SAR limits.

Structural, electrical, and optical properties of Si-doped ZnO thin films prepared via supercycled atomic layer deposition

Si-doped zinc oxide (ZnO) thin films were fabricated via atomic layer deposition (ALD) using diethylzinc, Tris(dimethylamino)silane, and H2O as Zn, Si, and O sources, respectively. The ALD cycle of the (Zn-O) step and the (Zn-Si-O) step were separated and the Si concentration was controlled via changing the (Zn-Si-O) pulse cycle compared to the (Zn-O) step. This Si source pulse sequence (Zn-Si-O) is different from the conventional (O-Si) pulse sequence and was specially selected in this study to maximize the properties of the thin film. All of the films showed the hexagonal wurtzite structure of ZnO with the (100) plane producing the main diffraction peak when ALD was performed at 200 ℃. As the Si-doping concentration increased, the crystallinity of the films deteriorated and the Scherrer size was reduced from 29.69 to 28.10 nm, there were improvements in the electrical characteristics, the carrier concentration increased up to 8.10 × 1020 cm−3, and the resistivity decreased to 5.15 × 10-4 Ω·cm, which is lower than the lowest previously reported result for Si-ZnO thin films fabricated via ALD (9.29 × 10-4 Ω·cm). Moreover, the carrier mobility increased at first (Si-ZnO 1:29 supercycles) and then decreased with increasing Si concentration. The average transmittance of all of the films was above 80% and the optical band gap increased from 3.29 to 3.47 eV. The increased carrier concentration according to the Burstein-Moss effect was linearly related to the band gap shift while up-shifting the EF (Fermi level) toward the conduction band. We expect that our approach in this study will provide an experimental basis to optimize ZnO thin-film characteristics via modification of Si pulsing sequence.

Post-mortem CMR in a model of sudden death due to myocardial ischemia: validation with connexin-43.

We sought to evaluate the effectiveness of post-mortem cardiac magnetic resonance (PM-CMR) for the identification of myocardial ischemia as cause of sudden cardiac death (SCD) when the time interval between the onset of ischemia and SCD is ≤ 90 min. PM-CMR was performed in 8 hearts explanted from pigs with spontaneous death caused by occlusion of the left anterior descending coronary artery: 4 with SCD after ≤ 40 min of coronary occlusion and 4 between 40 and 90 min. PM-CMR included conventional T1 and T2-weighted image and T1, T2, and T2* mapping techniques. Imaging data were compared and validated with immunohistochemical evaluation of the altered proportion and redistribution of phosphorylated versus non-phosphorylated connexin 43 (CX43 and npCX43, respectively), an established molecular marker of myocardial ischemia. At T2-weighted images, the ischemic core was hypointense (core/remote ratio 0.67 ± 0.11) and surrounded by and hyperintense border zone. Compared to remote myocardium, the ischemic core had higher T1 (p = 0.0008), and lower T2 (p = 0.007) and T2* (p = 0.002). Cytoplasmatic npX43 and the npCX43/CX43 ratio were significantly higher in animals deceased > 40 min than in others. PM-CMR can reliably detect early signs of myocardial damage induced by ischemia, based on conventional pulse sequences complemented by a novel ad hoc application of quantitative mapping techniques. • Post-mortem MRI may help to understand cause of sudden cardiac death. • Post-mortem MRI allows detection of signs of myocardial ischemia as cause of sudden cardiac death within 90 and 40 min following coronary occlusion as demonstrated in a pig model of myocardial ischemia. • Signs of myocardial ischemia using conventional and mapping MRI technique are associated with the immunohistochemical changes of phosphorylated and dephosphorylated connexin-43 which is an established molecular marker of myocardial ischemia.

A DNA-Based MRI Contrast Agent for Quantitative pH Measurement.

Extracellular pH is important in clinical measurements due to its correlation to cell metabolism and disease progression. In MRI, T1/T2 ratiometric analysis and other methods have been previously applied to quantify pH using conventional pulse sequences. However, for nanoparticle-based approaches, heterogeneity in size and surface functionalization tends toward qualitative rather than quantitative results. To address this limitation, we developed a novel DNA-based MRI contrast agent, pH-DMRCA, which utilizes a highly programmable and reproducible nanostructure. The pH-DMRCA is a dendritic DNA scaffold that is functionalized with a pH-responsive MRI-sensitive construct, Gd(NP-DO3A), at the end of each DNA arm. We first evaluated the r1 and r2 response of our pH-DMRCA over a range of pH values (pH = 5-9) to establish a relaxometric model of pH. These MRI-based assessments of pH were validated in a separate set of samples using a pH electrode (n = 18) and resulted in a good linear correlation (R2 = 0.99, slope = 0.98, intercept = 0). A Bland-Altman analysis of the results also showed reasonable agreement between the calculated pH and measured pH. Moreover, these pH comparisons were consistent across three different pH-DMRCA concentrations, demonstrating concentration-independence of the method. This MRI-based pH quantification methodology was further verified in human blood plasma. Given the versatility of the DNA-based nanostructures, the contrast agent has a potential to be applied to a wide variety of imaging applications where extracellular pH is important including cancer, stroke, cardiovascular disease, and other important diseases.

Relaxation-Enhanced Angiography without Contrast and Triggering (REACT) for pelvic MR venography in comparison to balanced gradient-echo and T2-weighted spin-echo techniques

Rationale and objectivesTo evaluate the imaging capabilities of the REACT pulse sequence in pelvic venous vessels compared to conventional non-contrast pulse sequences. Materials and methodsIn addition to routine MRI venography, non-contrast enhanced REACT pulse sequence was performed in 4 healthy volunteers and 21 patients with suspected or known deep venous thrombosis and post thrombotic syndrome. Acquired images were independently interpreted by two MRI radiologists. The sequence performance was subjectively evaluated on a four-point scale regarding the delineation of small peripheral, midsize and large proximal venous vessels, the imaging of vascular pathologies, and the degradation due to artifacts. To evaluate statistical differences in diagnostic accuracy Friedman's test with Dunn's correction was used. ResultsREACT depicted the peripheral veins superior to bTFE and T2-TSE with an average score of 3.39 compared to 2.33 in bTFE and 1.77 in T2-TSE. In midsize vessels REACT performed significantly better than T2-TSE (1.94) and bTFE (2.68) with a score of 3.64. For the large proximal vessels REACT (3.39), bTFE (3.33) and T2-TSE (3.56) performed equally without statistical difference. Visibility of venous pathologies was found to be equal between REACT (3.62), bTFE (3.51) and T2-TSE (3.52). The image degradation due to artifacts was rated best in T2-TSE (3.56), followed by REACT (3.39) and bTFE (3.33). ConclusionsREACT is a promising tool for the visualization of the pelvic venous system using magnetic resonance imaging.

Echo Trains in Pulsed Electron Spin Resonance of a Strongly Coupled Spin Ensemble.

We report on a novel dynamical phenomenon in electron spin resonance experiments of phosphorus donors. When strongly coupling the paramagnetic ensemble to a superconducting lumped element resonator, the coherent exchange between these two subsystems leads to a train of periodic, self-stimulated echoes after a conventional Hahn echo pulse sequence. The presence of these multiecho signatures is explained using a simple model based on spins rotating on the Bloch sphere, backed up by numerical calculations using the inhomogeneous Tavis-Cummings Hamiltonian.

Predicting PET-derived myelin content from multisequence MRI for individual longitudinal analysis in multiple sclerosis

Multiple sclerosis (MS) is a demyelinating and inflammatory disease of the central nervous system (CNS). The demyelination process can be repaired by the generation of a new sheath of myelin around the axon, a process termed remyelination. In MS patients, the demyelination–remyelination cycles are highly dynamic. Over the years, magnetic resonance imaging (MRI) has been increasingly used in the diagnosis of MS and it is currently the most useful paraclinical tool to assess this diagnosis. However, conventional MRI pulse sequences are not specific for pathological mechanisms such as demyelination and remyelination. Recently, positron emission tomography (PET) with radiotracer [11C]PIB has become a promising tool to measure in-vivo myelin content changes which is essential to push forward our understanding of mechanisms involved in the pathology of MS, and to monitor individual patients in the context of clinical trials focused on repair therapies. However, PET imaging is invasive due to the injection of a radioactive tracer. Moreover, it is an expensive imaging test and not offered in the majority of medical centers in the world. In this work, by using multisequence MRI, we thus propose a method to predict the parametric map of [11C]PIB PET, from which we derived the myelin content changes in a longitudinal analysis of patients with MS. The method is based on the proposed conditional flexible self-attention GAN (CF-SAGAN) which is specifically adjusted for high-dimensional medical images and able to capture the relationships between the spatially separated lesional regions during the image synthesis process. Jointly applying the sketch-refinement process and the proposed attention regularization that focuses on the MS lesions, our approach is shown to outperform the state-of-the-art methods qualitatively and quantitatively. Specifically, our method demonstrated a superior performance for the prediction of myelin content at voxel-wise level. More important, our method for the prediction of myelin content changes in patients with MS shows similar clinical correlations to the PET-derived gold standard indicating the potential for clinical management of patients with MS.

Implementation of a brain injury screen MRI for infants at risk for abusive head trauma.

Head computed tomography (CT) is the current standard of care for evaluating infants at high risk of abusive head trauma. To both assess the feasibility of using a previously developed magnetic resonance imaging (MRI) brain injury screen (MRBRscreen) in the acute care setting in place of head CT to identify intracranial hemorrhage in high-risk infants and to compare the accuracy of a rapid imaging pulse sequence (single-shot T2 fast spin echo [ssT2FSE]) to a conventional pulse sequence (conventional T2 fast spin echo [conT2FSE]). This was a quality improvement initiative to evaluate infants <12months of age who were screened for intracranial hemorrhage using an MRBRscreen as part of clinical care. The MRBRscreen included axial conT2FSE, axial gradient recalled echo, coronal T1-weighted inversion recovery, axial diffusion-weighted image and an axial ssT2FSE. A comparison of ssT2FSE to conT2FSE with respect to lesion detection was also performed. Of 158 subjects, the MRBRscreen was able to be completed in 155 (98%); 9% (14/155) were abnormal. Ninety-four percent (137/145) of subjects underwent only an MRBRscreen and avoided both radiation from head CT and sedation from MRI. The axial ssT2FSE and conT2FSE results were congruent 99% of the time. An MRBRscreen in place of a head CT is feasible and potentially could decrease head CT use by more than 90% in this population. Using a rapid ssT2FSE in place of a conT2FSE can reduce total scan time without losing lesion detection. If an MRBRscreen is readily available, physicians' threshold to perform neuroimaging may be lowered and lead to earlier detection of abusive head trauma.

A novel two-dimensional NMR relaxometry pulse sequence for petrophysical characterization of shale at low field.

Low field two-dimensional nuclear magnetic resonance (2D-NMR) relaxometry is a powerful probe for the characterization of heterogenous, porous media and provides geometrical, physical and chemical information about samples at a molecular level and has been widely used in shale studies. However, NMR signals of shale decay so rapidly, dry sample for particular, that the conventional two-dimensional pulse sequence is either not sensitive enough to short relaxation components or takes too much measurement time. In this paper, 2D-NMR relaxometry correlation based on partial inversion recovery CPMG (PIR-CPMG) pulse sequence is proposed and illustrated to improve the contrast over saturation recovery CPMG (SR-CPMG) and reduces the T1 encoding time of inversion recovery CPMG (IR-CPMG) for petrophysical characterization of shale. Subsequently, the kernel function and inversion method of this sequence are presented and the reliability of the inversion method is testified by numerical simulation. Next, theoretical analysis is conducted to validate the advantages of PIR-CPMG. Ultimately, experiments on copper sulfate solution, artificial sandstone, and shale samples are performed, respectively, to verify the feasibility and effectiveness of the proposed pulse sequence. The results demonstrate that the PIR-CPMG sequence is time-saving and high-contrast, especially for the short relaxation components. This pulse sequence can be utilized in bench-top NMR core analyzer and downhole well logging, potentially, to achieve integrated petrophysical characterization of shale.

Evaluation of cortical bone perfusion using dynamic contrast enhanced ultrashort echo time imaging: a feasibility study.

Dynamic contrast enhanced magnetic resonance imaging (DCE-MRI) has been used to study perfusion in a wide variety of soft tissues including the bone marrow. Study of perfusion in hard tissues such as cortical bone has been much more limited because of the lack of detectable MR signal from them using conventional pulse sequences. However, two-dimensional (2D) ultrashort echo time (UTE) sequences detect signal from cortical bone and allow fast imaging of this tissue. In addition, adiabatic 2D inversion recovery UTE (IR-UTE) sequences can provide excellent signal suppression of soft tissues, such as muscle and marrow, and allow cortical bone to be seen with high contrast and reduced artefacts. We aimed to assess the feasibility of using 2D UTE and 2D IR-UTE sequences to perform DCE-MRI in the cortical bone of rabbits and human volunteers. Cortical bone perfusion was studied in rabbits (n=12) and human volunteers (n=3) using 2D UTE and 2D IR-UTE sequences on a clinical 3T scanner. Dynamic data with an in-plane resolution of ~0.5×0.5 mm2, single slice thickness of 3 mm for rabbits and 10 mm for human volunteers, and temporal resolution of 23 s for 2D UTE imaging of rabbits, 28 s for 2D UTE imaging of human volunteers, and 60 s for 2D IR-UTE imaging of both the rabbits and human volunteers were acquired before and after the injection of a Gd contrast agent (Gd-BOPTA: Multihance; Bracco Imaging SpA, Milan, Italy). The dose was 0.06 mmol/kg for rabbits and 0.2 mmol/kg for human subjects. Kinetic analyses based on the Brix model, as well as simple calculations of maximum enhancement (ME) and enhancement slope (ES), were performed. The 12 rabbits showed a mean Ktrans of 0.36±0.07 min-1, Kep of 8.42±3.17 min-1, ME of 28.30±6.83, ES of 0.35±0.18 for the femur with the 2D UTE sequence, and a mean Ktrans of 0.45±0.10 min-1, Kep of 9.80±0.50 min-1, ME of 48.84±12.12, and ES of 0.69±0.27 for the femur with the 2D IR-UTE sequence. Lower ME and ES values were observed in the tibial midshaft of healthy human volunteers compared to rabbits. These results show that 2D UTE and 2D IR-UTE sequences are capable of detecting dynamic contrast enhancement in cortical bone in both rabbits and healthy human volunteers. Clinical studies with these techniques are likely to be feasible.

Metal About the Hip and Artifact Reduction Techniques: From Basic Concepts to Advanced Imaging.

Promising outcomes of hip replacement interventions in this era of aging populations have led to higher demands for hip arthroplasty procedures. These require effective methods and techniques for the detection of postoperative outcomes and complications. Based on the presence or absence of radiographic findings, magnetic resonance imaging (MRI) and computed tomography (CT) may be required to detect and further characterize different causes of failing implants. Yet metal-related artifacts degrade image quality and pose significant challenges for adequate image quality. To mitigate such artifacts in MRI, a set of techniques, collectively known as metal artifact reduction sequence (MARS) MRI, were developed that optimize the framework of the conventional pulse sequences and exploit novel multispectral and multispatial imaging methods such as Slice Encoding for Metal Artifact Correction (SEMAC) and Multi-Acquisition Variable-Resonance Image Combination (MAVRIC). Metal-induced artifacts on CT can be effectively reduced with virtual monochromatic reconstruction of dual-energy CT data sets, metal artifact reduction reconstruction algorithms, and postprocessing image visualization techniques.

Magnetohydrodynamic flow imaging of ionic solutions using electrical current injection and MR phase measurements.

In this study, a method is proposed to image magnetohydrodynamic (MHD) flow of ionic solutions, which is caused by externally injected electrical current to an imaging media, during MRI scans. A multi-physics (MP) model is created by using the electrical current, laminar flow, and MR equations. The conventional spoiled gradient echo MRI pulse sequence with bipolar flow encoding gradients is utilized to encode the MHD flow. Using the MP model and the MRI pulse sequence, relationship between the MHD flow related phase in the acquired MR signal, the injection current, and the MRI pulse sequence parameters is stated. Numerical simulations and physical experiments are performed to validate the proposed method. The simulation and experimental results are in agreement and show that the MHD flow related MR phase depends on the amplitude and duration of the flow encoding gradient and the injected current. This method may be used to evaluate the MHD flow of conductive liquid media during MRI scans with simultaneous electrical current injections. The MHD flow related MR phase is 1.5 radian for an injected current of 1 mA amplitude, 30 ms duration and a flow encoding gradient amplitude of 24 mT/m. This large MR phase range exhibits potential use of this method for clinical applications such as investigation of highly conductive cerebrospinal fluid (CSF) during clinical use of electrical current based neuromodulation in MRI. However, very high and time varying velocities of typical CSF flow compared to the MHD flow velocities should also be considered.