Molloy F M, Carr T D, Zeuner K E, Dambrosia J M, Hallett M
Human Motor Control Section, Medical Neurology Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892-1428, USA.
Brain. 2003 Oct;126(Pt 10):2175-82. doi: 10.1093/brain/awg219. Epub 2003 Jun 23.
Sensory processing is impaired in focal hand dystonia (FHD), with most previous studies having evaluated only the symptomatic limb. The purpose of this study was to establish whether the sensory system is affected in other types of dystonias and whether the contralateral hand is also involved in FHD. We used a spatial acuity measure (Johnson-Van Boven-Phillips domes) to evaluate sensory spatial discrimination in both hands of patients with different forms of dystonias including primary generalized DYT1 dystonia (associated with a unique deletion in the DYT1 gene) (n = 13), FHD (n = 15), benign essential blepharospasm (n = 9), cervical dystonia (n = 10) and in age-matched controls. Clinical evaluation included the Fahn dystonia scale for the focal dystonia groups and the Marsden-Burke-Fahn scale for the generalized dystonia group. Spatial discrimination was normal in patients with DYT1 dystonia, despite all of these patients having hand dystonia. However, spatial discrimination thresholds were significantly increased in both hands in the focal dystonia groups (thresholds were similar for each group) and did not correlate significantly with either severity or duration of dystonic symptoms. Thresholds were significantly increased in the dominant hand compared with the non-dominant hand only within the FHD group. Our observations demonstrate involvement of both the dominant and non-dominant somatosensory cortices, and suggest that abnormal sensory processing is a fundamental disturbance in patients with focal dystonia. These findings of altered sensory processing in idiopathic focal but not generalized DYT1 dystonia suggest both a primary pathophysiological role for the phenomenon in focal dystonia and divergent pathophysiological processes in the two conditions.
局灶性手部肌张力障碍(FHD)患者存在感觉加工障碍,以往大多数研究仅评估了出现症状的肢体。本研究的目的是确定感觉系统在其他类型的肌张力障碍中是否受到影响,以及对侧手部在FHD中是否也受累。我们使用空间敏锐度测量工具(约翰逊 - 范博温 - 菲利普斯圆顶)来评估不同形式肌张力障碍患者双手的感觉空间辨别能力,这些患者包括原发性全身性DYT1肌张力障碍(与DYT1基因的独特缺失相关)(n = 13)、FHD(n = 15)、良性原发性眼睑痉挛(n = 9)、颈部肌张力障碍(n = 10),并与年龄匹配的对照组进行比较。临床评估包括对局灶性肌张力障碍组使用法恩肌张力障碍量表,对全身性肌张力障碍组使用马斯登 - 伯克 - 法恩量表。DYT1肌张力障碍患者的空间辨别能力正常,尽管所有这些患者都有手部肌张力障碍。然而,局灶性肌张力障碍组双手的空间辨别阈值均显著升高(每组阈值相似),且与肌张力障碍症状的严重程度或持续时间均无显著相关性。仅在FHD组中,优势手的阈值相比非优势手显著升高。我们的观察结果表明,优势和非优势体感皮层均受累,并提示异常的感觉加工是局灶性肌张力障碍患者的一种基本障碍。特发性局灶性而非全身性DYT1肌张力障碍中感觉加工改变的这些发现表明,该现象在局灶性肌张力障碍中具有主要的病理生理作用,且在这两种情况下病理生理过程存在差异。