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体内高极化 C MRSI 的三维径向回波平面波谱成像。

Three-dimensional radial echo-planar spectroscopic imaging for hyperpolarized C MRSI in vivo.

机构信息

Division of Medical Physics in Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Faculty of Physics and Astronomy, University of Heidelberg, Heidelberg, Germany.

出版信息

Magn Reson Med. 2025 Jan;93(1):31-41. doi: 10.1002/mrm.30258. Epub 2024 Aug 20.

Abstract

PURPOSE

To demonstrate the feasibility of 3D echo-planar spectroscopic imaging (EPSI) technique with rapid volumetric radial k-space sampling for hyperpolarized (HP) C magnetic resonance spectroscopic imaging (MRSI) in vivo.

METHODS

A radial EPSI (rEPSI) was implemented on a 3 T clinical PET/MR system. To enable volumetric coverage, the sinusoidal shaped readout gradients per k-t-spoke were rotated along the three spatial dimensions in a golden-angle like manner. A distance-weighted, density-compensated gridding reconstruction was used, also in cases with undersampling of spokes in k-space. Measurements without and with HP C-labeled substances were performed in phantoms and rats using a double-resonant C/H volume resonator with 72 mm inner diameter.

RESULTS

Phantom measurements demonstrated the feasibility of the implemented rEPSI sequence, as well as the robustness to undersampling in k-space up to a factor of 5 without advanced reconstruction techniques. Applied to measurements with HP [1-C]pyruvate in a tumor-bearing rat, we obtained well-resolved MRSI datasets with a large matrix size of 12 voxels covering the whole imaging FOV of (180 mm) within 6.3 s, enabling to observe metabolism in dynamic acquisitions.

CONCLUSION

After further optimization, the proposed rEPSI method may be useful in applications of HP C-tracers where unknown or varying metabolite resonances are expected, and the acquisition of dynamic, volumetric MRSI datasets with an adequate temporal resolution is a challenge.

摘要

目的

展示三维 echo-planar 波谱成像 (EPSI) 技术与快速容积径向 k 空间采样相结合用于体内超极化 (HP) ¹³C 磁共振波谱成像 (MRSI) 的可行性。

方法

在 3T 临床 PET/MR 系统上实施了径向 EPSI (rEPSI)。为了实现容积覆盖,正弦形状的每个 k-t spokes 的读出梯度以类似于黄金角的方式沿着三个空间维度旋转。使用距离加权、密度补偿的网格重建,即使在 k 空间中 spokes欠采样的情况下也是如此。在使用具有 72mm 内径的双共振 C/H 体积谐振器的体模和大鼠中,分别进行了无和有 HP ¹³C 标记物质的测量。

结果

体模测量证明了所实施的 rEPSI 序列的可行性,以及在没有先进重建技术的情况下,在 k 空间中欠采样高达 5 倍的鲁棒性。将其应用于荷瘤大鼠中 HP [1-C]丙酮酸的测量,我们获得了分辨率良好的 MRSI 数据集,其大矩阵大小为 12 个体素,在 6.3s 内覆盖整个成像视场 (180mm),能够在动态采集时观察代谢。

结论

经过进一步优化,所提出的 rEPSI 方法可能在未知或变化的代谢物共振的情况下有用,并且在具有足够时间分辨率的动态、容积 MRSI 数据集的采集方面具有挑战性。

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