在标准回波时间和延长回波时间下,使用优化的点式编码时间缩减径向采集(PETRA)序列,在 7 特斯拉条件下进行超短波-T2*测绘

Carly A Lockard, Bruce M Damon, Hacene Serrai
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引用次数: 0

摘要

零回波时间(ZTE)序列可捕获T2*极短的组织信号,有助于对肌肉骨骼组织的超短T2*成分进行定性和定量成像。其中一个序列是点状编码时间缩短径向采集(PETRA)。虽然该序列显示出良好的效果,但在 7 特斯拉 (T) 下只进行了有限的测试。这项工作的目的是在 7 T 下评估 PETRA 的标准形式,并对序列进行修改,以延长回波时间,从而进行超短波-T2*映射。我们采集了 8 名参与者(5 名用于优化,3 名用于超短波-T2*绘图评估;5 男/3 女,39 +/- 11 岁)的氯化锰和胶原模型以及膝关节的 PETRA 图像。使用 1 个发射/28 个接收通道的膝关节线圈采集图像。对伪影、信号、信噪比(SNR)、超短波-T2*、相应的曲线拟合质量和重复性进行了评估。与传统 TE 序列(双回波稳态,TE = 2.55 毫秒)相比,TE = 0.07 毫秒时膝关节组织的信噪比较高,PETRA 评估组织的信噪比在 68 到 337 之间,而传统 TE 序列中相同组织感兴趣区的信噪比在 16 到 30 之间。在 1.50 毫米各向同性采集分辨率和 TE 小于或等于 0.58 毫秒的条件下,可以采集超短波-T2*图系列。在弛豫时间与氯化锰浓度之间以及信号与胶原蛋白浓度之间观察到强烈的线性相关。模型和膝关节超短波-T2* <1 毫秒的超短波-T2*信号衰减曲线拟合 R2 和重复性都很高。在 7T 下,TE = 0.07 毫秒时分辨率高(0.34 毫米各向同性),回波时间小于或等于 0.58 毫秒时分辨率低(1.52 毫米各向同性),PETRA 成像伪影极小,信噪比高,扫描时间为 11 分钟。超短波-T2*映射为亚毫秒T2*物质提供了可接受的曲线拟合结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultrashort-T2* mapping at 7 tesla using an optimized pointwise encoding time reduction with radial acquisition (PETRA) sequence at standard and extended echo times
Zero echo time (ZTE) sequences capture signal from tissues with extremely short T2* and are useful for qualitative and quantitative imaging of musculoskeletal tissues' ultrashort-T2* components. One such sequence is Pointwise Encoding Time Reduction with Radial Acquisition (PETRA). While this sequence has shown promising results, it has undergone only limited testing at 7 tesla (T). The purpose of this work was to evaluate PETRA at 7T in its standard form and with sequence modifications to allow extended echo times for the purpose of performing ultrashort-T2* mapping. We acquired PETRA images of MnCl2 and collagen phantoms and of the knee in eight participants (5 for optimization and 3 for ultrashort-T2* mapping assessment; 5 male/3 female, 39 +/- 11 years old). Images were acquired using a 1-transmit/28-receive-channel knee coil. Artifacts, signal, signal-to-noise ratio (SNR), ultrashort-T2*, the corresponding curve fit quality, and repeatability were assessed. SNR was high in knee tissues at TE = 0.07 msec compared to a conventional-TE sequence (Dual-Echo Steady State with TE = 2.55 msec), with values ranging between 68 to 337 across the assessed tissues for PETRA versus 16 to 30 for the same tissue regions of interest in the conventional-TE series. Acquisition of series for ultrashort-T2* maps was feasible at 1.50 mm isotropic acquisition resolution and TE less than or equal to 0.58 msec. Strong linear correlations were observed between relaxation times and MnCl2 concentration, and between signal and collagen concentration. Ultrashort-T2* signal decay curve fit R2 and repeatability were high for phantom and knee ultrashort-T2* <1 msec. PETRA imaging with minimal artifacts, high SNR, and scan time < 11 minutes was achieved at 7T at high (0.34 mm isotropic) resolution at TE = 0.07 msec and lower resolution (1.52 mm isotropic) at echo times less than or equal to 0.58 msec. Ultrashort-T2* mapping provided acceptable curve-fitting results for substances with sub-millisecond T2*.
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