基于深度学习重建的高加速高分辨率双反转恢复MR成像对多发性硬化皮质旁病变的改进评估

Tomohiro Shintaku, Satoru Ide, Haruka Nagaya, Yuka Ishimoto, Keita Watanabe, Kazuhiko Oyu, Sera Kasai, Yoshihito Umemura, Miho Sasaki, Kana Saito, Amo Ozawa, Atsushi Nozaki, Xucheng Zhu, Tetsuya Wakayama, Haruo Nishijima, Chieko Suzuki, Masahiko Tomiyama, Shingo Kakeda
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引用次数: 0

摘要

目的:最近,一种新的基于深度学习(DL)的技术被开发出来,用于重建高度欠采样的MR数据(DL- speed, DLS),该技术表现出优于压缩感知的性能。本研究旨在利用DLS (DLS-DIR)实现高分辨率双反转恢复(DIR)成像,并比较其对皮质旁多发性硬化症(MS)病变的诊断性能与常规DIR (C-DIR)。方法:我们回顾性分析了25例MS患者的MRI数据,这些患者接受了全面的成像方案,包括3D液体衰减反转恢复(FLAIR)、C-DIR和DLS-DIR。C-DIR采用尺寸为1.3 × 1.3 × 1.4 mm3的体素,扫描时间为3 min 55s; DLS-DIR采用各向同性0.7 mm体素,扫描时间为4 min 23s。两名神经放射学家在两次单独的阅读会话(一次使用C-DIR,另一次使用DLS-DIR)中评估皮质旁MS病变。病变分为皮层下白质病变、皮层内病变或皮层下白质和灰质混合病变。使用Wilcoxon符号秩检验比较不同成像技术之间每个区域的病变计数。结果:与C-DIR相比,DLS-DIR检测到的皮质旁MS病变数量显著增加(放射科医生a: 211个vs 164个;结论:DLS技术可以在5分钟的采集时间内实现高分辨率的全脑DLS- dir成像,可以无缝地纳入常规临床工作流程。这种方法大大提高了皮质旁MS病变的检测和评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improved Assessment of Juxtacortical Lesions in Multiple Sclerosis Using Highly-accelerated High-resolution Double Inversion Recovery MR Imaging with Deep Learning-based Reconstruction.

Purpose: Recently, a novel deep learning (DL)-based technique for reconstructing highly undersampled MR data (DL-Speed, DLS) has been developed, which demonstrated superior performance over compressed sensing. This study aimed to achieve high-resolution double inversion recovery (DIR) imaging using DLS (DLS-DIR) and compare its diagnostic performance in the detection of juxtacortical multiple sclerosis (MS) lesions with that of conventional DIR (C-DIR).

Methods: We retrospectively analyzed MRI data from 25 patients with MS who underwent a comprehensive imaging protocol, including 3D fluid-attenuated inversion recovery (FLAIR), C-DIR, and DLS-DIR. A voxel size of 1.3 × 1.3 × 1.4 mm3 with a scan duration of 3 mins 55s were used for C-DIR, and isotropic 0.7 mm voxels with a scan time of 4 mins 23s were employed for DLS-DIR. Two neuroradiologists assessed the juxtacortical MS lesions during 2 separate reading sessions (one with C-DIR and the other with DLS-DIR). Lesions were categorized as subcortical white matter lesions, intracortical lesions, or mixed lesions involving both subcortical white and gray matter. The lesion counts per region were compared between the imaging techniques using the Wilcoxon signed-rank test.

Results: DLS-DIR detected a significantly higher number of juxtacortical MS lesions compared to C-DIR (Radiologist A: 211 lesions vs. 164 lesions; Radiologist B: 209 lesions vs. 157 lesions, P < 0.05). DLS-DIR also identified more intracortical lesions (Radiologist A: 22 additional lesions, Radiologist B: 34 additional lesions, P < 0.05) and more mixed lesions (Radiologist A: 46 additional lesions, Radiologist B: 42 additional lesions, P < 0.05).

Conclusion: The DLS technology enables high-resolution, whole-brain DLS-DIR imaging within a 5 mins acquisition time, which can be seamlessly incorporated into routine clinical workflows. This approach substantially enhances the detection and evaluation of juxtacortical MS lesions.

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