Weiser Paul J, Langs Georg, Bogner Wolfgang, Motyka Stanislav, Strasser Bernhard, Golland Polina, Singh Nalini, Dietrich Jorg, Uhlmann Erik, Batchelor Tracy, Cahill Daniel, Hoffmann Malte, Klauser Antoine, Andronesi Ovidiu C
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA; Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA; Computational Imaging Research Lab - Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Computational Imaging Research Lab - Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Neuroimage. 2025 Apr 1;309:121045. doi: 10.1016/j.neuroimage.2025.121045. Epub 2025 Feb 1.
Altered neurometabolism is an important pathological mechanism in many neurological diseases and brain cancer, which can be mapped non-invasively by Magnetic Resonance Spectroscopic Imaging (MRSI). Advanced MRSI using non-cartesian compressed-sense acquisition enables fast high-resolution metabolic imaging but has lengthy reconstruction times that limits throughput and needs expert user interaction. Here, we present a robust and efficient Deep Learning reconstruction embedded in a physical model within an end-to-end automated processing pipeline to obtain high-quality metabolic maps.
Fast high-resolution whole-brain metabolic imaging was performed at 3.4 mm isotropic resolution with acquisition times between 4:11-9:21 min:s using ECCENTRIC pulse sequence on a 7T MRI scanner. Data were acquired in a high-resolution phantom and 27 human participants, including 22 healthy volunteers and 5 glioma patients. A deep neural network using recurring interlaced convolutional layers with joint dual-space feature representation was developed for deep learning ECCENTRIC reconstruction (Deep-ER). 21 subjects were used for training and 6 subjects for testing. Deep-ER performance was compared to iterative compressed sensing Total Generalized Variation reconstruction using image and spectral quality metrics.
Deep-ER demonstrated 600-fold faster reconstruction than conventional methods, providing improved spatial-spectral quality and metabolite quantification with 12%-45% (P<0.05) higher signal-to-noise and 8%-50% (P<0.05) smaller Cramer-Rao lower bounds. Metabolic images clearly visualize glioma tumor heterogeneity and boundary. Deep-ER generalizes reliably to unseen data.
Deep-ER provides efficient and robust reconstruction for sparse-sampled MRSI. The accelerated acquisition-reconstruction MRSI is compatible with high-throughput imaging workflow. It is expected that such improved performance will facilitate basic and clinical MRSI applications for neuroscience and precision medicine.
神经代谢改变是许多神经疾病和脑癌的重要病理机制,可通过磁共振波谱成像(MRSI)进行无创映射。使用非笛卡尔压缩感知采集的先进MRSI能够实现快速高分辨率代谢成像,但重建时间较长,限制了通量,并且需要专业用户交互。在此,我们提出了一种稳健且高效的深度学习重建方法,该方法嵌入到端到端自动处理管道中的物理模型中,以获得高质量的代谢图谱。
在7T MRI扫描仪上使用ECCENTRIC脉冲序列,以3.4毫米各向同性分辨率进行快速高分辨率全脑代谢成像,采集时间在4:11 - 9:21分钟之间。在高分辨率体模和27名人类参与者(包括22名健康志愿者和5名胶质瘤患者)中采集数据。开发了一种使用循环交错卷积层和联合双空间特征表示的深度神经网络,用于深度学习ECCENTRIC重建(Deep-ER)。21名受试者用于训练,6名受试者用于测试。使用图像和光谱质量指标将Deep-ER的性能与迭代压缩感知全广义变分重建进行比较。
Deep-ER的重建速度比传统方法快600倍,提供了更高的空间光谱质量和代谢物定量,信噪比提高了12% - 45%(P<0.05),克莱姆 - 拉奥下界降低了8% - 50%(P<0.05)。代谢图像清晰地显示了胶质瘤肿瘤的异质性和边界。Deep-ER能够可靠地推广到未见过的数据。
Deep-ER为稀疏采样的MRSI提供了高效且稳健的重建。加速采集 - 重建的MRSI与高通量成像工作流程兼容。预计这种改进的性能将促进神经科学和精准医学的基础和临床MRSI应用。