Patterns of EMG-EMG coherence in limb dystonia

被引:56
作者
Grosse, P
Edwards, M
Tijssen, MAJ
Schrag, A
Lees, AJ
Bhatia, KP
Brown, P
机构
[1] Inst Neurol, Sobell Dept Motor Neurosci & Movement Disorders, London WC1N 3BG, England
[2] UCL Natl Hosp Neurol & Neurosurg, London WC1N 3BG, England
[3] Acad Med Ctr, Amsterdam, Netherlands
[4] Charite Univ Med Berlin, Berlin, Germany
关键词
dystonia; DYT1; frequency analysis; coherence;
D O I
10.1002/mds.20075
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Dystonia of the limbs may be due to a wide range of aetiologies and may cause major functional limitation. We investigated whether the previously described pathological 4 to 7 Hz drive to muscles in cervical dystonia is present in patients with aetiologically different types of dystonia of the upper and lower limbs. To this end, we studied 12 symptomatic and 4 asymptomatic carriers of the DYT l gene, 6 patients with symptomatic dystonia due to focal basal ganglia lesions, and 11 patients with fixed dystonia, a condition assumed to be mostly psychogenic in aetiology. We evaluated EMG-EMG coherence in the tibialis anterior (TA) of these and 15 healthy control subjects. Ten of 12 (83%) of symptomatic DYT1 patients had an excessive 4 to 7 Hz common drive to TA, evident as an inflated coherence in this band. This drive also involved the gastrocnemius, leading to co-contracting electromyographic bursts. In contrast, asymptomatic DYT1 carriers, patients with symptomatic dystonia, patients with fixed dystonia, and healthy subjects showed no evidence of such a drive or any other distinguishing electrophysiological feature. Moreover, the pathological 4 to 7 Hz drive in symptomatic DYT1 patients was much less common in the upper limb, where it was only present in 2 of 6 (33%) patients with clinical involvement of the arms. We conclude that the nature of the abnormal drive to dystonic muscles may vary according to the, muscles under consideration and, particularly, with aetiology. (C) 2004 Movement Disorder Society.
引用
收藏
页码:758 / 769
页数:12
相关论文
共 49 条
[21]   Coupling of antagonistic ankle muscles during co-contraction in humans [J].
Hansen, S ;
Hansen, NL ;
Christensen, LOD ;
Petersen, NT ;
Nielsen, JB .
EXPERIMENTAL BRAIN RESEARCH, 2002, 146 (03) :282-292
[22]   Dynamics of tremor-related oscillations in the human globus pallidus: A single case study [J].
Hurtado, JM ;
Gray, CM ;
Tamas, LB ;
Sigvardt, KA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1674-1679
[23]   Abnormal cortical motor excitability in dystonia [J].
Ikoma, K ;
Samii, A ;
Mercuri, B ;
Wassermann, EM ;
Hallett, M .
NEUROLOGY, 1996, 46 (05) :1371-1376
[24]   DYSTONIA AND TREMOR INDUCED BY PERIPHERAL TRAUMA - PREDISPOSING FACTORS [J].
JANKOVIC, J ;
VANDERLINDEN, C .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1988, 51 (12) :1512-1519
[25]   TREMOR AND IDIOPATHIC DYSTONIA [J].
JEDYNAK, CP ;
BONNET, AM ;
AGID, Y .
MOVEMENT DISORDERS, 1991, 6 (03) :230-236
[26]   Symptomatic dystonias associated with structural brain lesions: Report of 16 cases [J].
Kostic, VS ;
StojanovicSvetel, M ;
Kacar, A .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1996, 23 (01) :53-56
[27]   PSYCHOGENIC DYSTONIA - A REVIEW OF 18 CASES [J].
LANG, AE .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1995, 22 (02) :136-143
[28]   Tremor-frequency (3-6 Hz) activity in the sensorimotor arm representation of the internal segment of the globus pallidus in patients with Parkinson's disease [J].
Lemstra, AW ;
Metman, LV ;
Lee, JI ;
Dougherty, PM ;
Lenz, FA .
NEUROSCIENCE LETTERS, 1999, 267 (02) :129-132
[29]   Involvement of the medial pallidum in focal myoclonic dystonia: A clinical and neurophysiological case study [J].
Liu, XG ;
Griffin, IC ;
Parkin, SG ;
Miall, C ;
Rowe, JG ;
Gregory, RP ;
Scott, RB ;
Aziz, TZ ;
Stein, JF .
MOVEMENT DISORDERS, 2002, 17 (02) :346-353
[30]   MUSCLE SPASMS ASSOCIATED WITH SUDECKS ATROPHY AFTER INJURY [J].
MARSDEN, CD ;
OBESO, JA ;
TRAUB, MM ;
ROTHWELL, JC ;
KRANZ, H ;
LACRUZ, F .
BRITISH MEDICAL JOURNAL, 1984, 288 (6412) :173-176