Structural connectivity-based topography of the human globus pallidus: Implications for therapeutic targeting in movement disorders

被引:41
作者
Cacciola, Alberto [1 ]
Milardi, Demetrio [1 ,2 ]
Bertino, Salvatore [1 ]
Basile, Gianpaolo Antonio [1 ]
Calamuneri, Alessandro [2 ]
Chillemi, Gaetana [2 ]
Rizzo, Giuseppina [1 ]
Anastasi, Giuseppe [1 ]
Quartarone, Angelo [1 ]
机构
[1] Univ Messina, Dept Biomed Dent Sci & Morphol & Funct Images, Via Consolare Valeria 1, I-98125 Messina, Italy
[2] Ctr Neurolesi Bonin Pulejo, IRCCS, Messina, Italy
关键词
basal ganglia; diffusion MRI; globus pallidus; movement disorders; topographic brain mapping; tractography; CONSTRAINED SPHERICAL DECONVOLUTION; DEEP-BRAIN-STIMULATION; IN-DIFFUSION MRI; BASAL GANGLIA; CEREBELLAR NETWORKS; NEURONAL-ACTIVITY; CEREBRAL-CORTEX; TRACTOGRAPHY; CIRCUITS; ORGANIZATION;
D O I
10.1002/mds.27712
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Understanding the topographical organization of the cortico-basal ganglia circuitry is of pivotal importance because of the spreading of techniques such as DBS and, more recently, MR-guided focused ultrasound for the treatment of movement disorders. A growing body of evidence has described both direct cortico- and dento-pallidal connections, although the topographical organization in vivo of these pathways in the human brain has never been reported. Objective To investigate the topographical organization of cortico- and dento-pallidal pathways by means of diffusion MRI tractography and connectivity based parcellation. Methods High-quality data from 100 healthy subjects from the Human Connectome Project repository were utilized. Constrained spherical deconvolution-based tractography was used to reconstruct structural cortico- and dento-pallidal connectivity. Connectivity-based parcellation was performed with a hypothesis-driven approach at three different levels: functional regions (limbic, associative, sensorimotor, and other), lobes, and gyral subareas. Results External globus pallidus segregated into a ventral associative cluster, a dorsal sensorimotor cluster, and a caudal "other" cluster on the base of its cortical connectivity. Dento-pallidal connections clustered only in the internal globus pallidus, where also associative and sensorimotor clusters were identified. Lobar parcellation revealed the presence in the external globus pallidus of dissociable clusters for each cortical lobe (frontal, parietal, temporal, and occipital), whereas in internal globus pallidus only frontal and parietal clusters were found out. Conclusion We mapped the topographical organization of both internal and external globus pallidus according to cortical and cerebellar connections. These anatomical data could be useful in DBS, radiosurgery and MR-guided focused ultrasound targeting for treating motor and nonmotor symptoms in movement disorders. (c) 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:987 / 996
页数:10
相关论文
共 81 条
  • [21] Pallidal versus Subthalamic Deep-Brain Stimulation for Parkinson's Disease
    Follett, Kenneth A.
    Weaver, Frances M.
    Stern, Matthew
    Hur, Kwan
    Harris, Crystal L.
    Luo, Ping
    Marks, William J., Jr.
    Rothlind, Johannes
    Sagher, Oren
    Moy, Claudia
    Pahwa, Rajesh
    Burchiel, Kim
    Hogarth, Penelope
    Lai, Eugene C.
    Duda, John E.
    Holloway, Kathryn
    Samii, Ali
    Horn, Stacy
    Bronstein, Jeff M.
    Stoner, Gatana
    Starr, Philip A.
    Simpson, Richard
    Baltuch, Gordon
    De Salles, Antonio
    Huang, Grant D.
    Reda, Domenic J.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 362 (22) : 2077 - 2091
  • [22] Behavioural disorders induced by external globus pallidus dysfunction in primates -: II.: Anatomical study
    François, C
    Grabli, D
    McCairn, K
    Jan, C
    Karachi, C
    Hirsch, EC
    Féger, J
    Tremblay, L
    [J]. BRAIN, 2004, 127 : 2055 - 2070
  • [23] Selective Activation of Striatal Fast-Spiking Interneurons during Choice Execution
    Gage, Gregory J.
    Stoetzner, Colin R.
    Wiltschko, Alexander B.
    Berke, Joshua D.
    [J]. NEURON, 2010, 67 (03) : 466 - 479
  • [24] NEURONAL POPULATION CODING OF MOVEMENT DIRECTION
    GEORGOPOULOS, AP
    SCHWARTZ, AB
    KETTNER, RE
    [J]. SCIENCE, 1986, 233 (4771) : 1416 - 1419
  • [25] New Roles for the External Globus Pallidus in Basal Ganglia Circuits and Behavior
    Gittis, Aryn H.
    Berke, Joshua D.
    Bevan, Mark D.
    Chan, C. Savio
    Mallet, Nicolas
    Morrow, Michelle M.
    Schmidt, Robert
    [J]. JOURNAL OF NEUROSCIENCE, 2014, 34 (46) : 15178 - 15183
  • [26] The minimal preprocessing pipelines for the Human Connectome Project
    Glasser, Matthew F.
    Sotiropoulos, Stamatios N.
    Wilson, J. Anthony
    Coalson, Timothy S.
    Fischl, Bruce
    Andersson, Jesper L.
    Xu, Junqian
    Jbabdi, Saad
    Webster, Matthew
    Polimeni, Jonathan R.
    Van Essen, David C.
    Jenkinson, Mark
    [J]. NEUROIMAGE, 2013, 80 : 105 - 124
  • [27] The external globus pallidus: progress and perspectives
    Hegeman, Daniel J.
    Hong, Ellie S.
    Hernandez, Vivian M.
    Chan, C. Savio
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2016, 43 (10) : 1239 - 1265
  • [28] Hoover JE, 1999, J NEUROSCI, V19, P1446
  • [29] The cerebellum communicates with the basal ganglia
    Hoshi, E
    Tremblay, L
    Féger, J
    Carras, PL
    Strick, PL
    [J]. NATURE NEUROSCIENCE, 2005, 8 (11) : 1491 - 1493
  • [30] Origins of multisynaptic projections from the basal ganglia to the forelimb region of the ventral premotor cortex in macaque monkeys
    Ishida, Hiroaki
    Inoue, Ken-ichi
    Takada, Masahiko
    Hoshi, Eiji
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2016, 43 (02) : 258 - 269