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局灶性肌张力障碍中感觉运动结构的形态计量学变化。

Morphometric changes of sensorimotor structures in focal dystonia.

作者信息

Obermann Mark, Yaldizli Ozguer, De Greiff Armin, Lachenmayer Martin Lenard, Buhl Anna Rebecca, Tumczak Felicitus, Gizewski Elke Ruth, Diener Hans-Christoph, Maschke Matthias

机构信息

Department of Neurology, University of Duisburg-Essen, Essen, Germany.

出版信息

Mov Disord. 2007 Jun 15;22(8):1117-23. doi: 10.1002/mds.21495.

Abstract

Idiopathic cervical dystonia (CD) and benign essential blepharospasm (BEB) are the most common forms of focal dystonia. Previous autopsy and imaging studies suggested that these disorders are not accompanied by structural brain abnormalities. However, recent brain voxel-based morphometry (VBM) studies of these conditions suggest that there actually may be changes in gray matter. The objective of this stdy was to detect possible gray matter abnormalities in patients with CD and BEB using VBM and to compare the results between the two conditions and with age- and gender-matched controls. High-resolution MRI was employed to evaluate healthy controls and individuals with BEB and CD. Eleven BEB, 9 CD, and 14 healthy control subjects were imaged. VBM revealed alterations of gray matter structures involved in sensorimotor processing in the individuals with focal dystonia. In CD subjects there was increased gray matter in the thalamus, caudate head bilaterally, superior temporal lobe, and left cerebellum, while gray matter was decreased in the putamen bilaterally. BEB subjects had increased gray matter in the caudate head and cerebellum bilaterally as well as decrease in the putamen and thalamus bilaterally. These findings strongly underline the recent notion that idiopathic focal dystonias might have a detectable structural correlate. They also demonstrate structural similarities of the investigated focal dystonias, possibly reflecting a shared common pathophysiological origin.

摘要

特发性颈部肌张力障碍(CD)和良性原发性眼睑痉挛(BEB)是局灶性肌张力障碍最常见的形式。以往的尸检和影像学研究表明,这些疾病并不伴有脑结构异常。然而,最近针对这些病症的基于体素的脑形态测量学(VBM)研究表明,实际上灰质可能存在变化。本研究的目的是使用VBM检测CD和BEB患者可能存在的灰质异常,并比较这两种病症之间以及与年龄和性别匹配的对照组之间的结果。采用高分辨率MRI对健康对照组以及患有BEB和CD的个体进行评估。对11名BEB患者、9名CD患者和14名健康对照者进行了成像。VBM显示,局灶性肌张力障碍患者中参与感觉运动处理的灰质结构发生了改变。在CD患者中,丘脑、双侧尾状核头部、颞上叶和左侧小脑的灰质增加,而双侧壳核的灰质减少。BEB患者双侧尾状核头部和小脑的灰质增加,双侧壳核和丘脑的灰质减少。这些发现有力地强调了最近的观点,即特发性局灶性肌张力障碍可能有可检测到的结构关联。它们还证明了所研究的局灶性肌张力障碍的结构相似性,可能反映了共同的病理生理起源。

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