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PURPOSE To introduce and investigate a method for free-breathing three-dimensional (3D) B1+ mapping of the human body at ultrahigh field (UHF), which can be used to generate homogenous flip angle (FA) distributions in the human body at UHF. METHODS A 3D relative B1+ mapping sequence with a radial phase-encoding (RPE) k-space trajectory was developed and applied in 11 healthy subjects at 7T. An RPE-based actual flip angle mapping method was applied with a dedicated B1+ shim setting to calibrate the relative B1+ maps yielding absolute B1+ maps of the individual transmit channels. The method was evaluated in a motion phantom and by multidimensional in vivo measurements. Additionally, 3D gradient echo scans with and without static phase-only B1+ shims were used to qualitatively validate B1+ shim predictions. RESULTS The phantom validation revealed good agreement for B1+ maps between dynamic measurement and static reference acquisition. The proposed 3D method was successfully validated in vivo by comparing magnitude and phase distributions with a 2D Cartesian reference. 3D B1+ maps free from visible motion artifacts were successfully acquired for 11 subjects with body mass indexes ranging from 19 kg/m2 to 34 kg/m2 . 3D respiration-resolved absolute B1+ maps indicated FA differences between inhalation and exhalation up to 15% for one channel and up to 24% for combined channels for shallow breathing. CONCLUSION The proposed method provides respiration-resolved absolute 3D B1+ maps of the human body at UHF, which enables the investigation and development of 3D B1+ shimming and parallel transmission methods to further enhance body imaging at UHF.

Purpose: Respiratory motion‐compensated (MC) 3D cardiac fat‐water imaging at 7T. Methods: Free‐breathing bipolar 3D triple‐echo gradient‐recalled‐echo (GRE) data with radial phase‐encoding (RPE) trajectory were acquired in 11 healthy volunteers (7M\4F, 21–35 years, mean: 30 years) with a wide range of body mass index (BMI; 19.9–34.0 kg/m2) and volunteer tailored B1+ shimming. The bipolar‐corrected triple‐echo GRE‐RPE data were binned into different respiratory phases (self‐navigation) and were used for the estimation of non‐rigid motion vector fields (MF) and respiratory resolved (RR) maps of the main magnetic field deviations (ΔB0). RR ΔB0 maps and MC ΔB0 maps were compared to a reference respiratory phase to assess respiration‐induced changes. Subsequently, cardiac binned fat‐water images were obtained using a model‐based, respiratory motion‐corrected image reconstruction. Results: The 3D cardiac fat‐water imaging at 7T was successfully demonstrated. Local respiration‐induced frequency shifts in MC ΔB0 maps are small compared to the chemical shifts used in the multi‐peak model. Compared to the reference exhale ΔB0 map these changes are in the order of 10 Hz on average. Cardiac binned MC fat‐water reconstruction reduced respiration induced blurring in the fat‐water images, and flow artifacts are reduced in the end‐diastolic fat‐water separated images. Conclusion: This work demonstrates the feasibility of 3D fat‐water imaging at UHF for the entire human heart despite spatial and temporal B1+ and B0 variations, as well as respiratory and cardiac motion.

Purpose MRI at ultra-high fields in the human body is highly challenging and requires lengthy calibration times to compensate for spatially heterogeneous B 1 + profiles. This study investigates the feasibility of using pre-computed universal pulses for calibration-free homogeneous 3D flip angle distribution in the human heart at 7T. Methods Twenty-two channel-wise 3D B 1 + data sets were acquired under free-breathing in 19 subjects to generate a library for an offline universal pulse (UP) design (group 1: 12 males [M] and 7 females [F], 21-66 years, 19.8-28.3 kg/m2 ). Three of these subjects (2M/1F, 21-33 years, 20.8-23.6 kg/m2 ) were re-scanned on different days. A 4kT-points UP optimized for the 22 channel-wise 3D B 1 + data sets in group 1 (UP22-4kT) is proposed and applied at 7T in 9 new and unseen subjects (group 2: 4M/5F, 25-56 years, 19.5-35.3 kg/m2 ). Multiple tailored and universal static and dynamic parallel-transmit (pTx) pulses were designed and evaluated for different permutations of the B 1 + data sets in group 1 and 2. Results The proposed UP22-4kT provides low B 1 + variation in all subjects, seen and unseen, without severe signal drops. Experimental data at 7T acquired with UP22-4kT shows comparable image quality as data acquired with tailored-4kT pulses and demonstrates successful calibration-free pTx of the human heart. Conclusion UP22-4kT allows for calibration-free homogeneous flip angle distributions across the human heart at 7T. Large inter-subject variations because of sex, age, and body mass index are well tolerated. The proposed universal pulse removes the need for lengthy (10-15 min) calibration scans and therefore has the potential to bring body imaging at 7T closer to the clinical application.

Three-dimensional (3D) human heart imaging at ultra-high fields is highly challenging due to respiratory and cardiac motion-induced artifacts as well as spatially heterogeneous B1+ profiles. In this study, we investigate the feasibility of applying 3D flip angle (FA) homogenization targeting the whole heart via static phase-only and dynamic kT-point in vivo parallel transmission at 7 T. 3D B1+ maps of the thorax were acquired under free breathing in eight subjects to compute parallel transmission pulses that improve excitation homogeneity in the human heart. To analyze the number of kT-points required, excitation homogeneity and radiofrequency (RF) power were compared using different regions of interest in six subjects with different body mass index (BMI) values of 20-34 kg/m2 for a wide range of regularization parameters. One subset of the optimized subject-specific pulses was applied in vivo on a 7 T scanner for six subjects in Cartesian 3D breath-hold scans as well as in two subjects in a radial phase-encoded 3D free-breathing scan. Across all subjects, 3-4 kT-points achieved a good tradeoff between RF power and nominal FA homogeneity. For subjects with a BMI in the normal range, the 4 kT-point pulses reliably improved the coefficient of variation by less than 10% compared with less than 25% achieved by static phase-only parallel transmission. in vivo measurements on a 7 T scanner validated the B1+ estimations and the pulse design, despite neglecting ΔB0 in the optimizations and Bloch simulations. This study demonstrates in vivo that kT-point pTx pulses are highly suitable for mitigating nominal FA heterogeneities across the entire 3D heart volume at 7 T. Furthermore, 3-4 kT-points demonstrate a practical tradeoff between nominal FA heterogeneity mitigation and RF power.