Hosey Tim P, Harding Sally G, Carpenter T Adrian, Ansorge Richard E, Williams Guy B
Department of Physics, Cavendish Laboratory, CB3 0HE Cambridge, UK.
Magn Reson Imaging. 2008 Feb;26(2):236-45. doi: 10.1016/j.mri.2007.07.002. Epub 2007 Sep 19.
A Markov chain Monte Carlo (MCMC) algorithm has been reported which is capable of determining the probabilistic orientation of two-fibre populations from high angular resolution diffusion-weighted data (HARDI). We present and critically discuss the application of this algorithm to in vivo human datasets acquired in clinically realistic times. We show that by appropriate model selection areas of multiple fibre populations can be identified that correspond with those predicted from known anatomy. Quantitative maps of fibre orientation probability are derived and shown for one- and two-fibre models of neural architecture. Fibre crossings in the pons, the internal capsule and the corona radiata are shown. In addition, we demonstrate that the relative proportion of anisotropic signal may be a more appropriate measure of anisotropy than summary measures derived from the tensor model such as fractional anisotropy in areas with multi-fibre populations.
已有报道称一种马尔可夫链蒙特卡罗(MCMC)算法能够根据高角分辨率扩散加权数据(HARDI)确定双纤维群的概率取向。我们展示并批判性地讨论了该算法在临床实际时间内采集的体内人类数据集上的应用。我们表明,通过适当的模型选择,可以识别出与已知解剖结构预测相对应的多个纤维群区域。推导并展示了神经结构的单纤维和双纤维模型的纤维取向概率定量图。展示了脑桥、内囊和放射冠中的纤维交叉情况。此外,我们证明,在具有多纤维群的区域中,各向异性信号的相对比例可能比从张量模型得出的汇总测量值(如分数各向异性)更适合作为各向异性的测量指标。