Impact of undersampling on preclinical lung T2* mapping with 3D radial UTE MRI at 7 T

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
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Abstract

Lung diseases are almost invariably heterogeneous and progressive, making it imperative to capture temporally and spatially explicit information to understand the disease initiation and progression. Imaging the lung with MRI—particularly in the preclinical setting—has historically been challenging because of relatively low lung tissue density, rapid cardiac and respiratory motion, and rapid transverse (T2*) relaxation. These limitations can largely be mitigated using ultrashort-echo-time (UTE) sequences, which are intrinsically robust to motion and avoid significant T2* decay. A significant disadvantage of common radial UTE sequences is that they require inefficient, center-out k-space sampling, resulting in long acquisition times relative to conventional Cartesian sequences. Therefore, pulmonary images acquired with radial UTE are often undersampled to reduce acquisition time. However, undersampling reduces image SNR, introduces image artifacts, and degrades true image resolution. The level of undersampling is further increased if offline gating techniques like retrospective gating are employed, because only a portion (∼40–50%) of the data is used in the final image reconstruction. Here, we explore the impact of undersampling on SNR and T2* mapping in mouse lung imaging using simulation and in-vivo data. Increased scatter in both metrics was noticeable at around 50% sampling. Parenchymal apparent SNR only decreased slightly (average decrease ∼ 1.4) with as little as 10% sampling. Apparent T2* remained similar across undersampling levels, but it became significantly increased (p < 0.05) below 80% sampling. These trends suggest that undersampling can generate quantifiable, but moderate changes in the apparent value of T2*. Moreover, these approaches to assess the impact of undersampling are straightforward to implement and can readily be expanded to assess the quantitative impact of other MR acquisition and reconstruction parameters.

Abstract Image

7 T 下三维径向 UTE MRI 的采样不足对临床前肺 T2* 映像的影响
肺部疾病几乎无一例外地具有异质性和进展性,因此必须捕捉明确的时间和空间信息,以了解疾病的起始和进展。由于肺组织密度相对较低、心脏和呼吸运动较快以及横向(T2*)弛豫较快,使用核磁共振成像(尤其是在临床前)对肺部进行成像历来具有挑战性。使用超短回波时间(UTE)序列可以在很大程度上缓解这些限制,因为UTE序列对运动具有固有的鲁棒性,并能避免明显的T2*衰减。普通径向UTE序列的一个明显缺点是需要低效的、中心向外的K空间采样,导致采集时间比传统的笛卡尔序列长。因此,使用径向UTE采集的肺部图像通常采用欠采样,以缩短采集时间。然而,欠采样会降低图像信噪比、引入图像伪影并降低真实图像分辨率。如果采用离线门控技术(如回溯门控),采样不足的程度会进一步增加,因为只有部分数据(40%-50%)会用于最终图像重建。在此,我们利用模拟和体内数据探讨了小鼠肺部成像中采样不足对信噪比和 T2* 映射的影响。采样率在 50%左右时,这两项指标的散度都明显增加。实质表观信噪比在采样率低至 10%时仅略有下降(平均下降 ∼ 1.4)。表观 T2* 在不同取样不足水平下保持相似,但在取样不足 80% 时显著增加(p < 0.05)。这些趋势表明,取样不足会对 T2* 的表观值产生可量化但适度的变化。此外,这些评估采样不足影响的方法简单易行,可随时扩展到评估其他磁共振采集和重建参数的定量影响。
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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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