IRCCS, Fondazione Don Carlo Gnocchi ONLUS, Via Alfonso Capecelatro, 66, 20148, Milan, Italy.
Department of Neurology, Wayne State University School of Medicine, 4201 St Antoine St, Detroit, MI 48201, USA.
Eur Radiol. 2021 Jul;31(7):4504-4513. doi: 10.1007/s00330-020-07515-z. Epub 2021 Jan 6.
The strategically acquired gradient echo (STAGE) protocol, developed for 3T scanners, allows one to derive quantitative maps such as T1, T2*, proton density, and quantitative susceptibility mapping in about 5 min. Our aim was to adapt the STAGE sequences for 1.5T scanners which are still commonly used in clinical practice. Furthermore, the accuracy and repeatability of the STAGE-derived T1 estimate were tested.
Flip angle (FA) optimization was performed using a theoretical simulation by maximizing signal-to-noise ratio, contrast-to-noise ratio, and T1 precision. The FA choice was further refined with the ISMRM/NIST phantom and in vivo acquisitions. The accuracy of the T1 estimate was assessed by comparing STAGE-derived T1 values with T1 maps obtained with an inversion recovery sequence. T1 accuracy was investigated for both the phantom and in vivo data. Finally, one subject was acquired 10 times once a week and a group of 27 subjects was scanned once. The T1 coefficient of variation (COV) was computed to assess scan-rescan and physiological variability, respectively.
The FA = 7°,38° were identified as the optimal FA pair at 1.5T. The T1 estimate errors were below 3% and 5% for phantom and in vivo measurements, respectively. COV for different tissues ranged from 1.8 to 4.8% for physiological variability, and between 0.8 and 2% for scan-rescan repeatability.
The optimized STAGE protocol can provide accurate and repeatable T1 mapping along with other qualitative images and quantitative maps in about 7 min on 1.5T scanners. This study provides the groundwork to assess the role of STAGE in clinical settings.
• The STAGE imaging protocol was optimized for use on 1.5T field strength scanners. • A practical STAGE protocol makes it possible to derive quantitative maps (i.e., T1, T2*, PD, and QSM) in about 7 min at 1.5T. • The T1 estimate derived from the STAGE protocol showed good accuracy and repeatability.
专为 3T 扫描仪开发的策略获取梯度回波(STAGE)协议可在大约 5 分钟内得出定量图谱,如 T1、T2*、质子密度和定量磁化率图。我们的目标是为仍在临床实践中广泛使用的 1.5T 扫描仪适配 STAGE 序列。此外,还测试了 STAGE 衍生 T1 估计的准确性和可重复性。
通过最大化信噪比、对比噪声比和 T1 精度,使用理论模拟进行翻转角(FA)优化。通过 ISMRM/NIST 体模和体内采集进一步优化 FA 选择。通过将 STAGE 衍生的 T1 值与反转恢复序列获得的 T1 图谱进行比较来评估 T1 估计的准确性。分别对体模和体内数据进行 T1 准确性研究。最后,对一名受试者每周采集 10 次,对 27 名受试者进行一次扫描。分别计算 T1 变异系数(COV)以评估扫描间和生理变异性。
在 1.5T 下,确定 FA=7°、38°为最佳 FA 对。在体模和体内测量中,T1 估计误差分别低于 3%和 5%。不同组织的 COV 生理变异性范围为 1.8%至 4.8%,扫描间重复性范围为 0.8%至 2%。
在 1.5T 扫描仪上,优化后的 STAGE 协议可以在大约 7 分钟内提供准确且可重复的 T1 映射以及其他定性图像和定量图谱。本研究为评估 STAGE 在临床环境中的作用奠定了基础。
• STAGE 成像协议在 1.5T 场强扫描仪上进行了优化。• 实际的 STAGE 协议可在大约 7 分钟内在 1.5T 下得出定量图谱(即 T1、T2*、PD 和 QSM)。• STAGE 协议得出的 T1 估计具有良好的准确性和可重复性。