Marcelo V. W. Zibetti, Rajiv Menon, Hector L. De Moura, Mahesh B. Keerthivasan, Ravinder R. Regatte
{"title":"优化MR脉冲序列用于高分辨率脑3D-T1ρ映射与加权自旋锁定获取。","authors":"Marcelo V. W. Zibetti, Rajiv Menon, Hector L. De Moura, Mahesh B. Keerthivasan, Ravinder R. Regatte","doi":"10.1002/mrm.30412","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Purpose</h3>\n \n <p>To implement and evaluate the feasibility of brain spin–lattice relaxation in the rotating frame (T1ρ) mapping using a novel optimized pulse sequence that incorporates weighted spin-lock acquisitions, enabling high-resolution three-dimensional (3D) mapping.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>The optimized variable flip-angle framework, previously proposed for knee T1ρ mapping, was enhanced by integrating weighted spin-lock acquisitions. This strategic combination significantly boosts signal-to-noise ratio (SNR) while reducing data acquisition time, facilitating high-resolution 3D-T1ρ mapping of the brain. The proposed sequence was compared with magnetization-prepared angle-modulated partitioned k-space spoiled gradient-echo sequence snapshots (MAPSS).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The newly developed pulse sequence, tested for brain 3D-T1ρ mapping for the first time, obtained maps in 4 min with quality comparable to a 20-min MAPSS sequence. Specifically, the voxel-wise median absolute percentage difference between these MR sequences at a resolution of 0.9 × 0.9 × 3 mm<sup>3</sup> is 13.1%. If high resolution is desired, with a voxel size of 0.5 × 0.5 × 3 mm<sup>3</sup>, the new sequence can acquire T1ρ maps in 8 min, surpassing a 20-min (and resolution of 0.9 × 0.9 × 3 mm<sup>3</sup>) MAPSS in SNR. The weighted spin-lock acquisition combined with optimized variable flip angle improved the SNR over optimized variable flip angle alone by about 28%.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Compared with the 20-min MAPSS sequence for brain T1ρ mapping, the proposed learned high-resolution 3D pulse sequence simultaneously achieved a 2.3-fold improvement in effective (3.2-fold nominal) spatial resolution, a 1.1-fold improvement in SNR, and a 2.5-fold reduction in scan time.</p>\n </section>\n </div>","PeriodicalId":18065,"journal":{"name":"Magnetic Resonance in Medicine","volume":"93 4","pages":"1458-1470"},"PeriodicalIF":3.0000,"publicationDate":"2024-12-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimized MR pulse sequence for high-resolution brain 3D-T1ρ mapping with weighted spin-lock acquisitions\",\"authors\":\"Marcelo V. W. Zibetti, Rajiv Menon, Hector L. De Moura, Mahesh B. Keerthivasan, Ravinder R. Regatte\",\"doi\":\"10.1002/mrm.30412\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Purpose</h3>\\n \\n <p>To implement and evaluate the feasibility of brain spin–lattice relaxation in the rotating frame (T1ρ) mapping using a novel optimized pulse sequence that incorporates weighted spin-lock acquisitions, enabling high-resolution three-dimensional (3D) mapping.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>The optimized variable flip-angle framework, previously proposed for knee T1ρ mapping, was enhanced by integrating weighted spin-lock acquisitions. This strategic combination significantly boosts signal-to-noise ratio (SNR) while reducing data acquisition time, facilitating high-resolution 3D-T1ρ mapping of the brain. The proposed sequence was compared with magnetization-prepared angle-modulated partitioned k-space spoiled gradient-echo sequence snapshots (MAPSS).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>The newly developed pulse sequence, tested for brain 3D-T1ρ mapping for the first time, obtained maps in 4 min with quality comparable to a 20-min MAPSS sequence. Specifically, the voxel-wise median absolute percentage difference between these MR sequences at a resolution of 0.9 × 0.9 × 3 mm<sup>3</sup> is 13.1%. If high resolution is desired, with a voxel size of 0.5 × 0.5 × 3 mm<sup>3</sup>, the new sequence can acquire T1ρ maps in 8 min, surpassing a 20-min (and resolution of 0.9 × 0.9 × 3 mm<sup>3</sup>) MAPSS in SNR. The weighted spin-lock acquisition combined with optimized variable flip angle improved the SNR over optimized variable flip angle alone by about 28%.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Compared with the 20-min MAPSS sequence for brain T1ρ mapping, the proposed learned high-resolution 3D pulse sequence simultaneously achieved a 2.3-fold improvement in effective (3.2-fold nominal) spatial resolution, a 1.1-fold improvement in SNR, and a 2.5-fold reduction in scan time.</p>\\n </section>\\n </div>\",\"PeriodicalId\":18065,\"journal\":{\"name\":\"Magnetic Resonance in Medicine\",\"volume\":\"93 4\",\"pages\":\"1458-1470\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-12-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Magnetic Resonance in Medicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mrm.30412\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magnetic Resonance in Medicine","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mrm.30412","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING","Score":null,"Total":0}
Optimized MR pulse sequence for high-resolution brain 3D-T1ρ mapping with weighted spin-lock acquisitions
Purpose
To implement and evaluate the feasibility of brain spin–lattice relaxation in the rotating frame (T1ρ) mapping using a novel optimized pulse sequence that incorporates weighted spin-lock acquisitions, enabling high-resolution three-dimensional (3D) mapping.
Methods
The optimized variable flip-angle framework, previously proposed for knee T1ρ mapping, was enhanced by integrating weighted spin-lock acquisitions. This strategic combination significantly boosts signal-to-noise ratio (SNR) while reducing data acquisition time, facilitating high-resolution 3D-T1ρ mapping of the brain. The proposed sequence was compared with magnetization-prepared angle-modulated partitioned k-space spoiled gradient-echo sequence snapshots (MAPSS).
Results
The newly developed pulse sequence, tested for brain 3D-T1ρ mapping for the first time, obtained maps in 4 min with quality comparable to a 20-min MAPSS sequence. Specifically, the voxel-wise median absolute percentage difference between these MR sequences at a resolution of 0.9 × 0.9 × 3 mm3 is 13.1%. If high resolution is desired, with a voxel size of 0.5 × 0.5 × 3 mm3, the new sequence can acquire T1ρ maps in 8 min, surpassing a 20-min (and resolution of 0.9 × 0.9 × 3 mm3) MAPSS in SNR. The weighted spin-lock acquisition combined with optimized variable flip angle improved the SNR over optimized variable flip angle alone by about 28%.
Conclusion
Compared with the 20-min MAPSS sequence for brain T1ρ mapping, the proposed learned high-resolution 3D pulse sequence simultaneously achieved a 2.3-fold improvement in effective (3.2-fold nominal) spatial resolution, a 1.1-fold improvement in SNR, and a 2.5-fold reduction in scan time.
期刊介绍:
Magnetic Resonance in Medicine (Magn Reson Med) is an international journal devoted to the publication of original investigations concerned with all aspects of the development and use of nuclear magnetic resonance and electron paramagnetic resonance techniques for medical applications. Reports of original investigations in the areas of mathematics, computing, engineering, physics, biophysics, chemistry, biochemistry, and physiology directly relevant to magnetic resonance will be accepted, as well as methodology-oriented clinical studies.