Movement-related cortical potentials in patients with Machado-Joseph disease

Clinical Neurophysiology

Volumn 119, Issue 5, 2008, Pages 1010-1019

  Lu, Ming Kuei ^a,b   Shih, Hsu Tzu ^a   Huang, Kai Ju ^a   Ziemann, Ulf ^b   Tsai, Chon Haw ^a,c,d   Chang, Fang Chia ^a,e   Chen, Ya Chu ^a   Lin, Yi Tsung ^d   Huang, Wei Shih ^a   Lee, Cheng Chun ^a,d   Liu, Chin San ^f  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

^b GOETHE UNIVERSITY   (Germany)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

^d CHINA MEDICAL UNIVERSITY   (Taiwan)

^e NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^f CHANGHUA CHRISTIAN HOSPITAL   (Taiwan)

Author keywords

Bereitschaftspotential; Cerebello thalamo cortical circuit; Machado Joseph disease (spinocerebellar ataxia type 3); Movement related cortical potential; Offset cortical potential; Post movement cortical potential

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONTINGENT NEGATIVE VARIATION; CONTROLLED STUDY; ELECTROENCEPHALOGRAM; ELECTROMYOGRAPHY; EVOKED MUSCLE RESPONSE; FEMALE; HUMAN; MACHADO JOSEPH DISEASE; MALE; MOTOR DYSFUNCTION; MOTOR PERFORMANCE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; VOLUNTARY MOVEMENT; WRIST;

ADULT; CEREBRAL CORTEX; ELECTROENCEPHALOGRAPHY; ELECTROMYOGRAPHY; EVOKED POTENTIALS, MOTOR; FEMALE; HUMANS; MACHADO-JOSEPH DISEASE; MALE; MOTOR ACTIVITY;

EID: 41449083857     PISSN: 13882457     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinph.2008.01.008     Document Type: Article

References (45)

1. Aleksandrov I.O., and Maksimova N.E. P300 and psychophysiological analysis of the structure of behavior. Electroenceph Clin Neurophysiol 61 (1985) 548-558
2. Babiloni C., Del Percio C., Babiloni F., Carducci F., Cincotti F., Moretti D.V., et al. Transient human cortical responses during the observation of simple finger movements: a high-resolution EEG study. Hum Brain Mapp 20 (2003) 148-157
3. Buhmann C., Bussopulos A., and Oechsner M. Dopaminergic response in Parkinsonian phenotype of Machado-Joseph disease. Mov Disord 18 (2003) 219-221
4. Colding-Jorgensen E., Sorensen S.A., Hasholt L., and Lauritzen M. Electrophysiological findings in a Danish family with Machado-Joseph disease. Muscle Nerve 19 (1996) 743-750
5. Deecke L. Electrophysiological correlates of movement initiation. Rev Neurol (Paris) 146 (1990) 612-619
6. Deiber M.P., Ibanez V., Sadato N., and Hallett M. Cerebral structures participating in motor preparation in humans: a positron emission tomography study. J Neurophysiol 75 (1996) 233-247
7. Deuschl G., Toro C., Matsumoto J., and Hallett M. Movement-related cortical potentials in writer's cramp. Ann Neurol 38 (1995) 862-868
8. Dick J.P.R., Rothwell J.C., Day B.L., Cantello R., Buruma O., Gioux M., et al. The Bereitschaftspotential is abnormal in Parkinson's disease. Brain 112 (1989) 233-244
9. Ghez C., and Thach W.T. The cerebellum. In: Kandel E.R., Schwartz J.H., and Jessell T.M. (Eds). Principles of neural science (2000), McGraw-Hill, United States of America 832-852
10. Ghisolfi E.S., Maegawa G.H.B., Becker J., Zanardo A.P., Strimitzer Jr. I.M., Prokopiuk A.S., et al. Impaired P50 sensory gating in Machado-Joseph disease. Clin Neurophysiol 115 (2004) 2231-2235
11. Hotson J.R., Langston E.B., Louis A.A., and Rosenberg R.N. The search for a physiologic marker of Machado-Joseph disease. Neurology 37 (1987) 112-116
12. Hulsmann E., Erb M., and Grodd W. From will to action: sequential cerebellar contributions to voluntary movement. Neuroimage 20 (2003) 1485-1492
13. Ikeda A., and Shibasaki H. Invasive recording of movement-related cortical potentials in humans. J Clin Neurophysiol 9 (1992) 509-520
14. Ikeda A., Luders H.O., Burgess R.C., and Shibasaki H. Movement-related potentials recorded from supplementary motor area and primary motor area. Role of supplementary motor area in voluntary movements. Brain 115 (1992) 1017-1043
15. Kawaguchi Y., Okamoto T., Taniwaki M., Aizawa M., Inoue M., Katayama S., et al. CAG expansions in a novel gene for Machado-Joseph disease at chromosone 14q32.1. Nat Genet 8 (1994) 221-228
16. Kobayashi T., and Kakizuka A. Molecular analyses of Machado-Joseph disease. Cytogenet Genome Res 100 (2003) 261-275
17. Kumada S., Hayashi M., Mizuguchi M., Nakano I., Morimatsu Y., and Oda M. Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease. Acta Neuropathol 99 (2000) 48-54
18. Matelli M., and Luppino G. Thalamic input to mesial and superior area 6 in the macaque monkey. J Comp Neurol 372 (1996) 59-87
19. Meyer-Lohmann J., Conrad B., Matsunami K., and Brooks V.B. Effects of dentate cooling on precentral unit activity following torque pulse injections into elbow movements. Brain Res 94 (1975) 237-251
20. Orioli P.J., and Strick P.L. Cerebellar connections with the motor cortex and the arcuate premotor area: an analysis employing retrograde transneuronal transport of WGA-HRP. J Comp Neurol 288 (1989) 612-626
21. Postert T., Eyding J., Berg D., Przuntek H., Becker G., Finger M., et al. Transcranial sonography in spinocerebellar ataxia type 3. J Neural Transm Suppl 68 (2004) 123-133
22. Rothwell J.C., Higuchi K., and Obeso J.A. The offset cortical potential: an electrical correlate of movement inhibition in man. Mov Disord 13 (1998) 330-335
23. Rub U., de Vos R.A., Brunt E.R., Schultz C., Paulson H., Del Tredici K., et al. Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease). Brain Res 953 (2002) 126-134
24. Rub U., de Vos R.A., Schultz C., Brunt E.R., Paulson H., and Braak H. Spinocerebellar ataxia type 3 (Machado-Joseph disease): severe destruction of the lateral reticular nucleus. Brain 125 (2002) 2115-2124
25. Sakai S.T., Inase M., and Tanji J. Pallidal and cerebellar inputs to thalamocortical neurons projecting to the supplementary motor area in Macaca fuscata: a triple-labeling light microscopic study. Anat Embryol 199 (1999) 9-19
26. Sakai S.T., Inase M., and Tanji J. The relationship between MI and SMA afferents and cerebellar and pallidal efferents in the macaque monkey. Somatosens Mot Res 19 (2002) 139-148
27. Shibasaki H., and Hallett M. What is the Bereitschaftspotential?. Clin Neurophysiol 117 (2006) 2341-2356
28. Shibasaki H., and Nagae K. Mirror movement: application of movement-related cortical potentials. Ann Neurol 15 (1984) 299-302
29. Shibasaki H., Shima F., and Kuroiwa Y. Clinical studies of the movement-related cortical potential (MP) and the relationship between the dentatorubrothalamic pathway and readiness potential (RP). J Neurol 219 (1978) 15-25
30. Shibasaki H., Barrett G., Halliday E., and Halliday A.M. Components of the movement-related cortical potential and their scalp topography. Electroenceph Clin Neurophysiol 49 (1980) 213-226
31. Shibasaki H., Barrett G., Neshige R., Hirata I., and Tomoda H. Volitional movement is not preceded by cortical slow negativity in cerebellar dentate lesion in man. Brain Res 368 (1986) 361-365
32. Shinotoh H., Thiessen B., Snow B.J., Hashimoto S., MacLeod P., Silveira I., et al. Fluorodopa and raclopride PET analysis of patients with Machado-Joseph disease. Neurology 49 (1997) 1133-1136
33. Spinella G.M., and Sheridan P.H. Research initiatives on Machado-Joseph disease: National Institute of Neurological Disorders and Stroke Workshop summary. Neurology 42 (1992) 2048-2051
34. Strick P.L. The influence of motor preparation on the response of cerebellar neurons to limb displacements. J Neurosci 3 (1983) 2007-2020
35. Tanji J., and Mushiake H. Comparison of neuronal activity in the supplementary motor area and primary motor cortex. Brain Res Cogn Brain Res 3 (1996) 143-150
36. Tarkka I.M., and Hallett M. Topography of scalp-recorded motor potentials in human finger movements. J Clin Neurophysiol 8 (1991) 331-341
37. Tarkka I.M., Massaquoi S., and Hallett M. Movement-related cortical potentials in patients with cerebellar degeneration. Acta Neurol Scand 88 (1993) 129-135
38. Tokumaru A.M., Kamakura K., Maki T., Murayama S., Sakata I., Kaji T., et al. Magnetic resonance imaging findings of Machado-Joseph disease: histopathologic correlation. J Comput Assist Tomogr 27 (2003) 241-248
39. Toma K., Honda M., Hanakawa T., Okada T., Fukuyama H., Ikeda A., et al. Activities of the primary and supplementary motor areas increase in preparation and execution of voluntary muscle relaxation: an event-related fMRI study. J Neurosci 19 (1999) 3527-3534
40. Wessel K., Verleger R., Nazarenus D., Vieregge P., and Kompf D. Movement-related cortical potentials preceding sequential and goal-directed finger and arm movements in patients with cerebellar atrophy. Electroenceph Clin Neurophysiol 92 (1994) 331-341
41. Yamada S., Nishimiya J., Nakajima T., and Taketazu F. Linear high intensity area along the medial margin of the internal segment of the globus pallidus in Machado-Joseph disease patients. J Neurol Neurosurg Psychiatry 76 (2005) 573-575
42. Yamaguchi S., and Knight R.T. Anterior and posterior association cortex contributions to the somatosensory P300. J Neurosci 11 (1991) 2039-2054
43. Yamamoto M., Kachi T., and Sobue G. Pain-related and electrically stimulated somatosensory evoked potentials in patients with Machado-Joseph disease and multiple system atrophy. Intern Med 36 (1997) 550-555
44. Yazawa S., Ikeda A., Kunieda T., Mima T., Nagamine T., Ohara S., et al. Human supplementary motor area is active in preparation for both voluntary muscle relaxation and contraction: subdural recording of Bereitschaftspotential. Neurosci Lett 244 (1998) 145-148
45. Yen T.C., Lu C.S., Tzen K.Y., Wey S.P., Chou Y.H., Weng Y.H., et al. Decreased dopamine transporter binding in Machado-Joseph disease. J Nucl Med 41 (2000) 994-998