Todd Nick, Moeller Steen, Auerbach Edward J, Yacoub Essa, Flandin Guillaume, Weiskopf Nikolaus
Wellcome Trust Centre for Neuroimaging, Institute of Neurology, University College London, London, United Kingdom.
Center for Magnetic Resonance Research, University of Minnesota, MN, United States.
Neuroimage. 2016 Jan 1;124(Pt A):32-42. doi: 10.1016/j.neuroimage.2015.08.056. Epub 2015 Sep 1.
Functional magnetic resonance imaging (fMRI) studies that require high-resolution whole-brain coverage have long scan times that are primarily driven by the large number of thin slices acquired. Two-dimensional multiband echo-planar imaging (EPI) sequences accelerate the data acquisition along the slice direction and therefore represent an attractive approach to such studies by improving the temporal resolution without sacrificing spatial resolution. In this work, a 2D multiband EPI sequence was optimized for 1.5mm isotropic whole-brain acquisitions at 3T with 10 healthy volunteers imaged while performing simultaneous visual and motor tasks. The performance of the sequence was evaluated in terms of BOLD sensitivity and false-positive activation at multiband (MB) factors of 1, 2, 4, and 6, combined with in-plane GRAPPA acceleration of 2× (GRAPPA 2), and the two reconstruction approaches of Slice-GRAPPA and Split Slice-GRAPPA. Sensitivity results demonstrate significant gains in temporal signal-to-noise ratio (tSNR) and t-score statistics for MB 2, 4, and 6 compared to MB 1. The MB factor for optimal sensitivity varied depending on anatomical location and reconstruction method. When using Slice-GRAPPA reconstruction, evidence of false-positive activation due to signal leakage between simultaneously excited slices was seen in one instance, 35 instances, and 70 instances over the ten volunteers for the respective accelerations of MB 2×GRAPPA 2, MB 4×GRAPPA 2, and MB 6×GRAPPA 2. The use of Split Slice-GRAPPA reconstruction suppressed the prevalence of false positives significantly, to 1 instance, 5 instances, and 5 instances for the same respective acceleration factors. Imaging protocols using an acceleration factor of MB 2×GRAPPA 2 can be confidently used for high-resolution whole-brain imaging to improve BOLD sensitivity with very low probability for false-positive activation due to slice leakage. Imaging protocols using higher acceleration factors (MB 3 or MB 4×GRAPPA 2) can likely provide even greater gains in sensitivity but should be carefully optimized to minimize the possibility of false activations.
功能磁共振成像(fMRI)研究若需要高分辨率全脑覆盖,则扫描时间较长,这主要是由采集的大量薄层图像所致。二维多频段回波平面成像(EPI)序列可加速沿层面方向的数据采集,因此通过在不牺牲空间分辨率的情况下提高时间分辨率,为这类研究提供了一种有吸引力的方法。在本研究中,针对3T场强下1.5mm各向同性全脑采集对二维多频段EPI序列进行了优化,并对10名健康志愿者在同时执行视觉和运动任务时进行成像。在多频段(MB)因子为1、2、4和6的情况下,结合2倍的面内GRAPPA加速(GRAPPA 2)以及Slice-GRAPPA和Split Slice-GRAPPA两种重建方法,从血氧水平依赖(BOLD)敏感性和假阳性激活方面对该序列的性能进行评估。敏感性结果表明,与MB 1相比,MB 2、4和6在时间信噪比(tSNR)和t分数统计方面有显著提高。最佳敏感性的MB因子因解剖位置和重建方法而异。使用Slice-GRAPPA重建时,在10名志愿者中,对于MB 2×GRAPPA 2、MB 4×GRAPPA 2和MB 6×GRAPPA 2各自的加速情况,分别有1例、35例和70例出现因同时激发层面间信号泄漏导致的假阳性激活证据。使用Split Slice-GRAPPA重建可显著抑制假阳性的发生率,在相同的加速因子下分别为1例、5例和5例。使用MB 2×GRAPPA 2加速因子的成像方案可放心用于高分辨率全脑成像,以提高BOLD敏感性,且因层面泄漏导致假阳性激活的概率非常低。使用更高加速因子(MB 3或MB 4×GRAPPA 2)的成像方案可能会在敏感性上有更大提升,但应仔细优化以尽量减少假激活的可能性。