Magnetic Resonance in Medicine最新文献

{"title":"In vivo simultaneous proton resonance frequency shift thermometry and single reference variable flip angle T1 measurements","authors":"Nicholas Richards,&nbsp;Michael Malmberg,&nbsp;Henrik Odéen,&nbsp;Sara Johnson,&nbsp;Michelle Kline,&nbsp;Robb Merrill,&nbsp;Rock Hadley,&nbsp;Dennis L. Parker,&nbsp;Allison Payne","doi":"10.1002/mrm.30413","DOIUrl":"10.1002/mrm.30413","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>The single reference variable flip angle sequence with a multi-echo stack of stars acquisition (SR-VFA-SoS) simultaneously measures temperature change using proton resonance frequency (PRF) shift and T₁-based thermometry methods. This work evaluates SR-VFA-SoS thermometry in MR-guided focused ultrasound in an in vivo rabbit model.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Simultaneous PRF shift thermometry and T₁-based thermometry were obtained in a New Zealand white rabbit model (<i>n</i> = 7) during MR-guided focused ultrasound surgery using the SR-VFA-SoS sequence at 3 T. Distinct locations in muscle (<i>n</i> = 16), fat (<i>n</i> = 12), or the interface of both tissues (<i>n</i> = 23) were heated. The T₁-temperature coefficient of fat was determined using least-squares fitting of inversion recovery-based T₁ maps of untreated fat harvested from the animal and was applied to the in vivo measured heat-induced T₁ changes to create temperature maps.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Using k-space weighted image contrast reconstruction, temporal resolution of 1.71 s was achieved for simultaneous thermometry at 1.5 × 1.5 × 2 mm voxel resolution. PRF shift thermometry was not sensitive to heating in fat. T₁ changes were observed in fat at the ultrasound focus. The mean T₁-temperature coefficient for fat was determined to be 1.9%/°C ± 0.2%/°C. Precision was 0.76°C ± 0.18°C for PRF shift thermometry in muscle and 1.93°C ± 0.60°C for T₁-based thermometry in fat. Sonications in muscle showed an increase in T₁ of 2.4%/°C ± 0.9%/°C.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The SR-VFA-SoS sequence was shown to simultaneously measure temperature change using PRF shift and T₁-based methods in an in vivo model, providing thermometry for both aqueous and fat tissues.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 5","pages":"2070-2085"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30413","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007907","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Learning-based motion artifact correction in the Z-spectral domain for chemical exchange saturation transfer MRI","authors":"Munendra Singh,&nbsp;Sultan Z. Mahmud,&nbsp;Vivek Yedavalli,&nbsp;Jinyuan Zhou,&nbsp;David Olayinka Kamson,&nbsp;Peter van Zijl,&nbsp;Hye-Young Heo","doi":"10.1002/mrm.30440","DOIUrl":"10.1002/mrm.30440","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>To develop and evaluate a physics-driven, saturation contrast-aware, deep-learning-based framework for motion artifact correction in CEST MRI.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A neural network was designed to correct motion artifacts directly from a Z-spectrum frequency (Ω) domain rather than an image spatial domain. Motion artifacts were simulated by modeling 3D rigid-body motion and readout-related motion during k-space sampling. A saturation-contrast-specific loss function was added to preserve amide proton transfer (APT) contrast, as well as enforce image alignment between motion-corrected and ground-truth images. The proposed neural network was evaluated on simulation data and demonstrated in healthy volunteers and brain tumor patients.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The experimental results showed the effectiveness of motion artifact correction in the Z-spectrum frequency domain (MOCO_Ω) compared to in the image spatial domain. In addition, a temporal convolution applied to a dynamic saturation image series was able to leverage motion artifacts to improve reconstruction results as a denoising process. The MOCO_Ω outperformed existing techniques for motion correction in terms of image quality and computational efficiency. At 3 T, human experiments showed that the root mean squared error (RMSE) of APT images decreased from 4.7% to 2.1% at 1 μT and from 6.2% to 3.5% at 1.5 μT in case of “moderate” motion and from 8.7% to 2.8% at 1 μT and from 12.7% to 4.5% at 1.5 μT in case of “severe” motion, after motion artifact correction.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The MOCO_Ω could effectively correct motion artifacts in CEST MRI without compromising saturation transfer contrast.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"94 1","pages":"331-345"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30440","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Phantom-based gradient waveform measurements with compensated variable-prephasing: Description and application to EPI at 7 T","authors":"Hannah Scholten,&nbsp;Tobias Wech,&nbsp;Istvan Homolya,&nbsp;Herbert Köstler","doi":"10.1002/mrm.30425","DOIUrl":"10.1002/mrm.30425","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>Introducing compensated variable-prephasing (CVP), a phantom-based method for gradient waveform measurements. The technique is based on the variable-prephasing (VP) method, but takes into account the effects of all gradients involved in the measurement.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We conducted measurements of a trapezoidal test gradient and of an EPI readout gradient train with three approaches: VP, CVP, and fully compensated variable-prephasing (FCVP). We compared them to one another and to predictions based on the gradient system transfer function. Furthermore, we used the measured and predicted EPI gradients for trajectory corrections in phantom images on a 7 T scanner.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The VP gradient measurements are confounded by lingering oscillations of the prephasing gradients, which are compensated in the CVP and FCVP measurements. FCVP is vulnerable to a sign asymmetry in the gradient chain. However, the trajectories determined by all three methods resulted in comparably high EPI image quality.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>We present a new approach allowing for phantom-based gradient waveform measurements with high precision, which can be useful for trajectory corrections in non-Cartesian or single-shot imaging techniques. In our experimental setup, the proposed “compensated variable-prephasing” method provided the most reliable gradient measurements of the different techniques we compared.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 5","pages":"2209-2223"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30425","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007913","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The proton resonance enhancement for CEST imaging and shift exchange (PRECISE) family of RF pulse shapes for CEST MRI","authors":"Zinia Mohanta,&nbsp;Julia Stabinska,&nbsp;Assaf A. Gilad,&nbsp;Peter B. Barker,&nbsp;Michael T. McMahon","doi":"10.1002/mrm.30410","DOIUrl":"10.1002/mrm.30410","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>To optimize a 100 ms pulse for producing CEST MRI contrast and evaluate in mice.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A gradient ascent algorithm was employed to generate a family of 100 point, 100 ms pulses for use in CEST pulse trains (proton resonance enhancement for CEST imaging and shift exchange). Gradient ascent optimizations were performed for exchange rates = 500, 1500, 2500, 3500, and 4500 s⁻¹; and labile proton offsets (Δω) = 9.6, 7.8, 4.2, and 2.0 ppm. Seven proton resonance enhancement for CEST imaging and shift exchange pulse shapes were tested on an 11.7 T scanner using a phantom containing three representative CEST agents with peak saturation B_1,peak = 4 μT. The pulse producing the most contrast in phantoms was then evaluated for CEST MRI pH mapping of the kidneys in healthy mice after iopamidol administration.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The most promising pulse in terms of contrast performance across all three phantoms was the 9.6 ppm, 2500 s⁻¹ optimized pulse with ˜2.7 × increase in asymmetric magnetization transfer ratio (MTR_asym) over Gaussian, and ˜ 1.3 times over Fermi pulses for the same B_1,peak = 4 μT. This pulse also displayed a large improvement in contrast over the Gaussian pulse after administration of iopamidol in live mice.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>A new 100-ms pulse was developed based on gradient ascent optimizations, which produced better contrast compared to standard Gaussian and Fermi pulses in phantoms. This shape also showed a substantial improvement for CEST MRI pH mapping in live mice over the Gaussian shape and appears promising for a wide range of CEST applications.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 5","pages":"1954-1968"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007919","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Enhanced detection of glutamate via transverse relaxation encoding with narrowband decoupling in the human brain","authors":"Li An,&nbsp;Sungtak Hong,&nbsp;Tara Turon,&nbsp;Adriana Pavletic,&nbsp;Christopher S. Johnson,&nbsp;John A. Derbyshire,&nbsp;Jun Shen","doi":"10.1002/mrm.30431","DOIUrl":"10.1002/mrm.30431","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>This study aims to improve the detection of glutamate (Glu) concentration and T₂ using an enhanced transverse relaxation encoding with narrowband decoupling (TREND) technique.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A new editing pulse was designed to simultaneously invert both Glu H3 spins (2.12 ppm and 2.05 ppm) while minimizing the excitation of Glu H4. Additionally, a frequency band was created to invert the lactate (Lac) H2 spin (4.10 ppm) while saturating the NAA aspartyl H2 spin (4.38 ppm). Numerical simulations compared Glu and Lac signals using the original and new editing pulses. In vivo experiments were conducted on healthy participants at 7 T to validate this enhanced TREND technique.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Numerical simulations showed prominently enhanced Glu and Lac resonance signals with the new editing pulse. In vivo spectra showed a 47% ± 14% increase in Glu/Cr peak amplitude ratios with the new editing pulse. Using the enhanced TREND sequence, Glu/Cr concentration ratios in the anterior cingulate cortex were 1.03 ± 0.07 with Cramer-Rao lower bounds (CRLBs) of 1.1% ± 0.1%, and Glu T₂ values were 179 ± 18 ms with CRLBs of 1.2% ± 0.1%. The Lac/Cr concentration ratios in the same voxels were 0.05 ± 0.01 with CRLBs of 26% ± 14%, and Lac T₂ values were 196 ± 23 ms with CRLBs of 22% ± 15%.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The new editing pulse significantly enhanced the detection of Glu and enabled the detection of Lac using TREND for measuring both the concentration and T₂ of the markers of oxidative metabolism and glycolysis.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 6","pages":"2278-2286"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30431","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Composite spin probes with adjustable oxygen sensitivity for pulse electron paramagnetic resonance imaging","authors":"Irene Canavesi,&nbsp;Navin Viswakarma,&nbsp;Raman Khurana,&nbsp;Boris Epel,&nbsp;Periannan Kuppusamy,&nbsp;Mark David Pagel,&nbsp;Mrignayani Kotecha","doi":"10.1002/mrm.30418","DOIUrl":"10.1002/mrm.30418","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>Solid crystalline spin probes, such as lithium phthalocyanine (LiPc) and lithium octa-n-butoxynaphthalocyanine (LiNc-BuO), allow repeated oxygen measurement using electron paramagnetic resonance (EPR). Due to their short relaxation times, their use for pulse EPR oxygen imaging is limited. In this study, we developed and tested a new class of solid composite spin probes that modified the relaxation rates R₁ and R₂ of LiPc or LiNc-BuO probes, which allowed pO₂ measurements in the full dynamic (0–760 torr) range.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>The composite probes were developed by embedding LiPc or LiNc-BuO with bonewax, beeswax, or petroleum jelly. All experiments were performed using a 25-mT EPR imager, JIVA-25®. A selected composite probe, LiPc-BW5 (LiPc + 5-times bonewax), was tested for its in vivo stability and robustness using oxygen-enhanced EPR oxygen imaging. As another application, a LiPc-BW5-based marker was tested to outline the SCC7 tumor in a C3H mouse.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>The composite probes showed an increased oxygen measurement range compared with unaltered probes. The in vivo experiments with LiPc-BW5 showed the stability of the probes for repeated oxygen imaging up to 4 weeks of measurements. The in vivo pO₂ at the subcutaneous site changed from 26.1 ± 1.9 torr to 118.9 ± 1.9 torr when the breathing gas was changed from 21% O₂ to 100% O₂. The use of LiPc-BW5 as a fiducial marker showed its use in outlining the tumor boundaries.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>We developed a new class of robust and versatile solid composite probes with adjustable oxygen sensitivity that allows pO₂ imaging in the broad dynamic range.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 5","pages":"2239-2249"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007899","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Three-dimensional whole-body imaging of the bioreduction and clearance of nitroxide probes in the thoracic and abdominal regions of mice using a compact and mobile electron paramagnetic resonance imager","authors":"Hideo Sato-Akaba,&nbsp;Miho C. Emoto,&nbsp;Hirotada G. Fujii","doi":"10.1002/mrm.30432","DOIUrl":"10.1002/mrm.30432","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>Redox homeostasis plays a key role in regulating the overall health and development of organisms. This study aimed to develop a compact and mobile continuous-wave (CW) electron paramagnetic resonance (EPR) imager to facilitate stable, highly sensitive fast three-dimensional (3D) whole-body imaging of nitroxide-infused mice.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A multiturn loop gap resonator with a diameter of 30 mm and length of 35 mm was designed for whole-body EPR imaging. A compact and mobile CW-EPR imager operating at 750 MHz was developed using this resonator. The automatic matching and tuning control systems were also adjusted to compensate for perturbations caused by the movement of the mice.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>When the mice were inserted into the resonator, the resonant frequency was easily determined for all parts of the mouse, from the head to the lower abdomen. 3D EPR images of the mouse body from the thoracic region to the lower abdomen were obtained following infusion of a nitroxide, 3-carboxy-2,2,5,5-tetramethylpyrrolidine-1-oxyl (CxP). The EPR images clearly visualized the CxP distribution in various organs at different concentrations. Time-dependent EPR images also revealed that the signal intensities of the CxP decayed over time, and the decay rates for the heart, liver, and kidneys were evaluated.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>A compact and mobile EPR imager that enables 3D whole-body EPR image of nitroxide in mice was developed. The EPR imager exhibited long-term stability against motion effects caused by respiratory motion and heartbeats in mice. The EPR images clearly visualized the in vivo distribution, clearance, and metabolism of the nitroxide in organs.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"94 1","pages":"424-435"},"PeriodicalIF":3.0,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007922","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Simultaneous multislice diffusion imaging using navigator-free multishot spiral acquisitions","authors":"Yuancheng Jiang,&nbsp;Guangqi Li,&nbsp;Xin Shao,&nbsp;Hua Guo","doi":"10.1002/mrm.30427","DOIUrl":"10.1002/mrm.30427","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>This work aims to raise a novel design for navigator-free multiband (MB) multishot uniform-density spiral (UDS) acquisition and reconstruction, and to demonstrate its utility for high-efficiency, high-resolution diffusion imaging.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Theory and Methods</h3>\u0000 \u0000 <p>Our design focuses on the acquisition and reconstruction of navigator-free MB multishot UDS diffusion imaging. For acquisition, radiofrequency-pulse encoding was used to achieve controlled aliasing in parallel imaging in MB imaging. For reconstruction, a new algorithm named slice–projection onto convex sets–enhanced inherent correction of phase errors (slice-POCS-ICE) was proposed to simultaneously estimate diffusion-weighted images and intershot phase variations for each slice. The efficacy of the proposed methods was evaluated in both numerical simulation and in vivo experiments.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>In both numerical simulation and in vivo experiments, slice-POCS-ICE estimated phase variations more precisely and provided results with better image quality than other methods. The intershot phase variations and MB slice aliasing artifacts were simultaneously resolved using the proposed slice-POCS-ICE algorithm.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The proposed navigator-free MB multishot UDS acquisition and reconstruction method is an effective solution for high-efficiency, high-resolution diffusion imaging.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"94 1","pages":"73-88"},"PeriodicalIF":3.0,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007855","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Quantifying spatial and dynamic lung abnormalities with 3D PREFUL FLORET UTE imaging: A feasibility study","authors":"Filip Klimeš,&nbsp;Joseph W. Plummer,&nbsp;Matthew M. Willmering,&nbsp;Alexander M. Matheson,&nbsp;Abdullah S. Bdaiwi,&nbsp;Marcel Gutberlet,&nbsp;Andreas Voskrebenzev,&nbsp;Marius M. Wernz,&nbsp;Frank Wacker,&nbsp;Jason Woods,&nbsp;Zackary I. Cleveland,&nbsp;Laura L. Walkup,&nbsp;Jens Vogel-Claussen","doi":"10.1002/mrm.30416","DOIUrl":"10.1002/mrm.30416","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>Pulmonary MRI faces challenges due to low proton density, rapid transverse magnetization decay, and cardiac and respiratory motion. The fermat-looped orthogonally encoded trajectories (FLORET) sequence addresses these issues with high sampling efficiency, strong signal, and motion robustness, but has not yet been applied to phase-resolved functional lung (PREFUL) MRI—a contrast-free method for assessing pulmonary ventilation during free breathing. This study aims to develop a reconstruction pipeline for FLORET UTE, enhancing spatial resolution for three-dimensional (3D) PREFUL ventilation analysis.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>The FLORET sequence was used to continuously acquire data over 7 ± 2 min in 36 participants, including healthy subjects (<i>N</i> = 7) and patients with various pulmonary conditions (<i>N</i> = 29). Data were reconstructed into respiratory images using motion-compensated low-rank reconstruction, and a 3D PREFUL algorithm was adapted to quantify static and dynamic ventilation surrogates. Image sharpness and signal-to-noise ratio were evaluated across different motion states. PREFUL ventilation metrics were compared with static ¹²⁹Xe ventilation MRI.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Optimal image sharpness and accurate ventilation dynamics were achieved using 24 respiratory bins, leading to their use in the study. A strong correlation was found between 3D PREFUL FLORET UTE ventilation defect percentages (VDPs) and ¹²⁹Xe VDPs (r ≥ 0.61, <i>p</i> &lt; 0.0001), although PREFUL FLORET static VDPs were significantly higher (mean bias = −10.1%, <i>p</i> &lt; 0.0001). In diseased patients, dynamic ventilation parameters showed greater heterogeneity and better alignment with ¹²⁹Xe VDPs.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The proposed reconstruction pipeline for FLORET UTE MRI offers improved spatial resolution and strong correlation with ¹²⁹Xe MRI, enabling dynamic ventilation quantification that may reveal airflow abnormalities in lung disease.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 5","pages":"1984-1998"},"PeriodicalIF":3.0,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30416","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007850","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"TagGen: Diffusion-based generative model for cardiac MR tagging super resolution","authors":"Changyu Sun,&nbsp;Cody Thornburgh,&nbsp;Yu Wang,&nbsp;Senthil Kumar,&nbsp;Talissa A. Altes","doi":"10.1002/mrm.30422","DOIUrl":"10.1002/mrm.30422","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Purpose</h3>\u0000 \u0000 <p>The aim of the work is to develop a cascaded diffusion-based super-resolution model for low-resolution (LR) MR tagging acquisitions, which is integrated with parallel imaging to achieve highly accelerated MR tagging while enhancing the tag grid quality of low-resolution images.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We introduced TagGen, a diffusion-based conditional generative model that uses low-resolution MR tagging images as guidance to generate corresponding high-resolution tagging images. The model was developed on 50 patients with long-axis-view, high-resolution tagging acquisitions. During training, we retrospectively synthesized LR tagging images using an undersampling rate (R) of 3.3 with truncated outer phase-encoding lines. During inference, we evaluated the performance of TagGen and compared it with REGAIN, a generative adversarial network–based super-resolution model that was previously applied to MR tagging. In addition, we prospectively acquired data from 6 subjects with three heartbeats per slice using 10-fold acceleration achieved by combining low-resolution <i>R</i> = 3.3 with GRAPPA-3 (generalized autocalibrating partially parallel acquisitions 3).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>For synthetic data (<i>R</i> = 3.3), TagGen outperformed REGAIN in terms of normalized root mean square error, peak signal-to-noise ratio, and structural similarity index (<i>p</i> &lt; 0.05 for all). For prospectively 10-fold accelerated data, TagGen provided better tag grid quality, signal-to-noise ratio, and overall image quality than REGAIN, as scored by two (blinded) radiologists (<i>p</i> &lt; 0.05 for all).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>We developed a diffusion-based generative super-resolution model for MR tagging images and demonstrated its potential to integrate with parallel imaging to reconstruct highly accelerated cine MR tagging images acquired in three heartbeats with enhanced tag grid quality.</p>\u0000 </section>\u0000 </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"94 1","pages":"362-372"},"PeriodicalIF":3.0,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/mrm.30422","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143007916","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}