Putamen volume in idiopathic focal dystonia

被引:75
作者
Black, KJ
Ongur, D
Perlmutter, JS
机构
[1] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Neurol & Neurol Surg, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[5] Washington Univ, Med Ctr, Mallinckrodt Inst Radiol, St Louis, MO 63110 USA
关键词
D O I
10.1212/WNL.51.3.819
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine whether the volume of the putamen is abnormal in patients with idiopathic focal dystonia. Background: The cause of adult-onset focal dystonia is unknown, but substantial evidence suggests that the putamen may be abnormal in this condition. Cell loss and gliosis have been suggested. We hypothesized that this might be reflected as abnormal putamen volume on MRI. Design and methods: A high-resolution MRI was acquired in 13 adults with cranial or hand dystonia and 13 normal individuals matched for age and sex. Putamen volume was measured using a stereologic method (Study 1). In a replication study, another rater measured putamen volume using manual tracing and direct voxel count (Study 2). Neither rater was aware of the diagnosis, and the order of measurement was random in each study. Results: In Study 1, putamen measurements were reasonably accurate (coefficient of error, similar to 6%). The putamen was 13% larger in patients, both in absolute terms (p = 0.03) and after covarying total brain volume (p = 0.02). In Study 2, putamen volumes correlated with those measured in Study 1 (intraclass correlation coefficient, 0.68 to 0.83). The putamen was 8% larger in patients (p = 0.06) and was larger in the patient than in the matched control subject in 10 of 13 pairs (p = 0.046). Conclusion: We find no evidence of putaminal atrophy or degeneration in adult-onset idiopathic focal dystonia, In fact, in this group, the putamen is about 10% larger in patients than in matched control subjects. This finding may reflect a response to the dystonia or may relate to its cause.
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页码:819 / 824
页数:6
相关论文
共 35 条
[1]   STRIATAL AND NIGRAL NEURON SUBPOPULATIONS IN RIGID HUNTINGTONS-DISEASE - IMPLICATIONS FOR THE FUNCTIONAL-ANATOMY OF CHOREA AND RIGIDITY-AKINESIA [J].
ALBIN, RL ;
REINER, A ;
ANDERSON, KD ;
PENNEY, JB ;
YOUNG, AB .
ANNALS OF NEUROLOGY, 1990, 27 (04) :357-365
[2]  
ARNDT S, 1991, PSYCHIAT RES-NEUROIM, V40, P79
[3]   THE BEHAVIORAL AND MOTOR CONSEQUENCES OF FOCAL LESIONS OF THE BASAL GANGLIA IN MAN [J].
BHATIA, KP ;
MARSDEN, CD .
BRAIN, 1994, 117 :859-876
[4]  
BUCHSBAUM MS, 1997, INT S NEUR NEUR ASS
[5]   SELECTIVE PUTAMINAL EXCITOTOXIC LESIONS IN NONHUMAN-PRIMATES MODEL THE MOVEMENT DISORDER OF HUNTINGTON DISEASE [J].
BURNS, LH ;
PAKZABAN, P ;
DEACON, TW ;
BROWNELL, AL ;
TATTER, SB ;
JENKINS, BG ;
ISACSON, O .
NEUROSCIENCE, 1995, 64 (04) :1007-1017
[6]   A primate genesis model of focal dystonia and repetitive strain injury .1. Learning-induced dedifferentiation of the representation of the hand in the primary somatosensory cortex in adult monkeys [J].
Byl, NN ;
Merzenich, MM ;
Jenkins, WM .
NEUROLOGY, 1996, 47 (02) :508-520
[7]   OVERACTIVE PREFRONTAL AND UNDERACTIVE MOTOR CORTICAL AREAS IN IDIOPATHIC DYSTONIA [J].
CEBALLOSBAUMANN, AO ;
PASSINGHAM, RE ;
WARNER, T ;
PLAYFORD, ED ;
MARSDEN, CD ;
BROOKS, DJ .
ANNALS OF NEUROLOGY, 1995, 37 (03) :363-372
[8]  
Chakos M. H., 1997, Society for Neuroscience Abstracts, V23, P2415
[9]   Movement-related cortical potentials in writer's cramp [J].
Deuschl, G ;
Toro, C ;
Matsumoto, J ;
Hallett, M .
ANNALS OF NEUROLOGY, 1995, 38 (06) :862-868
[10]  
EGGERS R, 1984, J HIRNFORSCH, V25, P129