Topography of cortical and subcortical connections of the human pedunculopontine and subthalamic nuclei

被引:139
作者
Aravamuthan, B. R.
Muthusamy, K. A.
Stein, J. F.
Aziz, T. Z.
Johansen-Berg, H.
机构
[1] Univ Oxford, Dept Physiol Anat & Genet, Oxford OX1 3PT, England
[2] NINDS, Bethesda, MD 20892 USA
[3] Radcliffe Infirm, Dept Neurol Surg, Oxford OX2 6HE, England
[4] John Radcliffe Hosp, Oxford Ctr Funct MRI Brain, Oxford OX3 9DU, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
D O I
10.1016/j.neuroimage.2007.05.050
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Deep brain stimulation (DBS) ofthe subthalamic nucleus (STN) is the most common surgical therapy for Parkinson' s disease (PD). DBS of the pedunculopontine nucleus (PPN) is emerging as a promising surgical therapy for PD as well. In order to better characterize these nuclei in humans, we determined the anatomical connections of the PPN and STN and the topography of these connections using probabilistic diffusion tractography. Diffusion tractography was carried out in eight healthy adult subjects using diffusion data acquired at 1.5 T MRI (60 directions, b=1000 S/MM2, 2x2x2 MM3 voxels). The major connections that we identified from single seed voxels within STN or PPN were present in at least half the subjects and the topography of these connections within a 36-voxel region surrounding the initial seed voxel was then examined. Both the PPN and STN showed connections with the cortex, basal ganglia, cerebellum, and down the spinal cord, largely matching connections demonstrated in primates. The topography of motor and associative brain areas in the human STN was strikingly similar to that shown in animals. PPN Topography has not been extensively demonstrated in animals, but we showed significant topography of cortical and subcortical connections in the human PPN. In addition to demonstrating the usefulness ofPDT in determining the connections and topography of small grey matter structures in vivo, these results allow for inference of optimal DBS target locations and add to our understanding of the role of these nuclei in PD. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:694 / 705
页数:12
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