Center for Pulmonary Imaging Research, Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Division of Pulmonary, Critical Care, and Sleep Medicine, University of Kansas Medical Center, Kansas City, Kansas.
NMR Biomed. 2021 Mar;34(3):e4464. doi: 10.1002/nbm.4464. Epub 2020 Dec 23.
Hyperpolarized (HP) Xe MRI is increasingly used to noninvasively probe regional lung structure and function in the preclinical setting. As in human imaging, the primary barrier to quantitative imaging with HP gases is nonequilibrium magnetization, which is depleted by T relaxation and radio frequency excitation. Preclinical HP gas imaging commonly involves mechanically ventilating small animals and encoding k-space over tens or hundreds of breaths, with small subsets of k-space data collected within each breath. Breath-to-breath magnetization renewal enables the use of large flip angles, but the resulting magnetization decay generates large view-to-view differences in within-breath signal intensity, leading to artifacts and degraded image quality. This deleterious signal decay has motivated the use of variable flip angle (VFA) sampling schemes, in which the flip angle is progressively increased to maintain constant view-to-view signal intensity. However, VFA imaging complicates data acquisition and provides only a global correction that fails to compensate for regional differences in signal dynamics. When constant flip angle (CFA) imaging is used alongside 3D radial golden means acquisition, the center of k-space is sampled with every excitation, thereby encoding signal dynamics alongside imaging data. Here, keyhole reconstruction is used to generate multiple images to capture in-breath HP Xe signal dynamics in mice and thus provide flip angle maps to quantitatively correct images without extra data collection. These CFA images display SNR that is not significantly different from VFA images, and further, high frequency k-space scaling can be used to mitigate decay-induced image artifacts. Results are supported by point spread function calculations and simulations of radial imaging with preclinical signal dynamics. Together, these results show that CFA 3D radial golden means ventilation imaging provides comparable image quality with VFA in small animals and allows for keyhole reconstruction, which can be used to generate flip angle maps and correct images for signal depletion.
高极化(HP)氙磁共振成像越来越多地用于在临床前环境中无创探测区域性肺结构和功能。与人成像一样,HP 气体定量成像的主要障碍是不平衡磁化,它通过 T 弛豫和射频激发而耗尽。临床前 HP 气体成像通常涉及机械通气小动物并在数十或数百次呼吸中对 k 空间进行编码,每次呼吸中仅采集 k 空间数据的一小部分。呼吸间磁化更新使大翻转角得以使用,但由此产生的磁化衰减导致呼吸内信号强度的视图间差异较大,从而产生伪影和图像质量下降。这种有害的信号衰减促使使用可变翻转角(VFA)采样方案,其中翻转角逐渐增加以保持视图间信号强度恒定。然而,VFA 成像使数据采集复杂化,并且仅提供全局校正,无法补偿信号动力学的区域差异。当与 3D 径向金均值采集一起使用恒翻转角(CFA)成像时,k 空间的中心在每次激发时都被采样,从而与成像数据一起编码信号动力学。在这里,关键孔重建用于生成多个图像以捕获呼吸内 HP 氙信号动力学,从而提供翻转角图来定量校正图像而无需额外的数据采集。这些 CFA 图像显示的 SNR 与 VFA 图像没有显著差异,此外,还可以使用高频 k 空间缩放来减轻衰减引起的图像伪影。结果得到点扩散函数计算和临床前信号动力学的径向成像模拟的支持。总之,这些结果表明,CFA 3D 径向金均值通气成像在小动物中具有与 VFA 相当的图像质量,并允许使用关键孔重建生成翻转角图并校正信号损耗图像。