Philips Technologie GmbH, Innovative Technologies, Research Laboratories, Hamburg, Germany.
Magn Reson Med. 2011 Oct;66(4):1116-22. doi: 10.1002/mrm.22877. Epub 2011 Mar 9.
Fluorine MRI offers broad potential for specific detection and quantification of molecularly targeted agents in diagnosis and therapy planning or monitoring. Because non-proton MRI applications lack morphological information, accompanying proton images are needed to elucidate the spatial tissue context. Furthermore, low concentrations typical of targeted molecular imaging agents require long examinations for signal averaging during which physiological motion may lead to blurring, underestimation in signal quantification, and erroneous localization of the agent distribution. Novel methods for truly simultaneous acquisition of dual-nuclei MR data are presented that offer efficient and precise anatomical localization of fluorine signals using accurate motion correction based on contemporaneous proton signals. The feasibility of simultaneous dual-nuclei MRI motion correction and corresponding dual-resolution reconstruction, providing nuclei-specific spatial resolution to retrospectively optimize the balance between signal-to-noise ratio and resolution, is shown on a clinical 3 T MR system.
氟磁共振成像在诊断和治疗计划或监测中具有广泛的潜力,可以特异性检测和定量靶向分子探针。由于非质子磁共振成像应用缺乏形态学信息,需要伴随质子图像来阐明空间组织背景。此外,由于靶向分子成像探针的浓度通常较低,需要进行长时间的信号平均以获得足够的信噪比,在此期间,生理运动可能导致图像模糊、信号定量低估以及探针分布的错误定位。本研究提出了一种真正的双核磁共振数据同步采集方法,该方法利用基于同期质子信号的精确运动校正,实现了氟信号的高效和精确的解剖定位。在临床 3 T 磁共振系统上,研究证明了同步双核磁共振成像运动校正和相应的双分辨率重建的可行性,该方法可以提供核特异性空间分辨率,以回顾性优化信噪比和分辨率之间的平衡。