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采用 3D-QALAS 与波 CAIPI 读出的高效、高分辨率 3T 全脑 relaxometry。

Time-efficient, high-resolution 3T whole-brain relaxometry using 3D-QALAS with wave-CAIPI readouts.

机构信息

Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, Massachusetts, USA.

Department of Radiology, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Magn Reson Med. 2024 Feb;91(2):630-639. doi: 10.1002/mrm.29865. Epub 2023 Sep 14.

Abstract

PURPOSE

Volumetric, high-resolution, quantitative mapping of brain-tissue relaxation properties is hindered by long acquisition times and SNR challenges. This study combines time-efficient wave-controlled aliasing in parallel imaging (wave-CAIPI) readouts with the 3D quantification using an interleaved Look-Locker acquisition sequence with a T preparation pulse (3D-QALAS), enabling full-brain quantitative T , T , and proton density (PD) maps at 1.15-mm isotropic voxels in 3 min.

METHODS

Wave-CAIPI readouts were embedded in the standard 3D-QALAS encoding scheme, enabling full-brain quantitative parameter maps (T , T , and PD) at acceleration factors of R = 3 × 2 with minimum SNR loss due to g-factor penalties. The quantitative parameter maps were estimated using a dictionary-based mapping algorithm incorporating inversion efficiency and B -field inhomogeneity effects. The parameter maps using the accelerated protocol were quantitatively compared with those obtained from the conventional 3D-QALAS sequence using GRAPPA acceleration of R = 2 in the ISMRM/NIST phantom, and in 10 healthy volunteers.

RESULTS

When tested in both the ISMRM/NIST phantom and 10 healthy volunteers, the quantitative maps using the accelerated protocol showed excellent agreement against those obtained from conventional 3D-QALAS at R  = 2.

CONCLUSION

Three-dimensional QALAS enhanced with wave-CAIPI readouts enables time-efficient, full-brain quantitative T , T , and PD mapping at 1.15 mm in 3 min at R = 3 × 2 acceleration. The quantitative maps obtained from the accelerated wave-CAIPI 3D-QALAS protocol showed very similar values to those from the standard 3D-QALAS (R = 2) protocol, alluding to the robustness and reliability of the proposed method.

摘要

目的

容积、高分辨率、脑组织结构弛豫特性的定量映射受到采集时间长和 SNR 挑战的限制。本研究结合了高效的波控混叠并行成像(wave-CAIPI)读出技术和使用带 T 准备脉冲的 3D 定量 Look-Locker 采集序列(3D-QALAS)进行 3D 定量,能够在 3 分钟内以 1.15mm 的各向同性体素获得全脑定量 T1、T2 和质子密度(PD)图。

方法

将 wave-CAIPI 读出技术嵌入到标准的 3D-QALAS 编码方案中,在最小 SNR 损失的情况下,利用 g 因子惩罚的全脑定量参数图(T1、T2 和 PD),加速因子 R=3×2。使用基于字典的映射算法来估计定量参数图,该算法包含反转效率和 B 场不均匀性的影响。使用加速协议获得的参数图与在 ISMRM/NIST 体模和 10 名健康志愿者中使用 GRAPPA 加速 R=2 的常规 3D-QALAS 序列获得的参数图进行定量比较。

结果

在 ISMRM/NIST 体模和 10 名健康志愿者中进行测试时,加速协议获得的定量图与常规 3D-QALAS 在 R=2 时获得的定量图具有极好的一致性。

结论

通过增强 wave-CAIPI 读出技术的 3D-QALAS 能够在 3 分钟内以 1.15mm 的分辨率,在 R=3×2 加速时实现高效、全脑定量 T1、T2 和 PD 映射。加速的 wave-CAIPI 3D-QALAS 协议获得的定量图与标准 3D-QALAS(R=2)协议获得的定量图非常相似,这表明了所提出方法的稳健性和可靠性。

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