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纹状体形态与颈部肌张力障碍患者未受影响亲属的感觉异常相关。

Striatal morphology correlates with sensory abnormalities in unaffected relatives of cervical dystonia patients.

作者信息

Walsh Richard A, Whelan Robert, O'Dwyer John, O'Riordan Sean, Hutchinson Siobhan, O'Laoide Risteard, Malone Kevin, Reilly Richard, Hutchinson Michael

机构信息

Department of Neurology, St. Vincent's University Hospital, Elm Park, Dublin 4, Ireland.

出版信息

J Neurol. 2009 Aug;256(8):1307-13. doi: 10.1007/s00415-009-5119-1. Epub 2009 Apr 8.

Abstract

Structural grey matter abnormalities have been described in adult-onset primary torsion dystonia (AOPTD). Altered spatial discrimination thresholds are found in familial and sporadic AOPTD and in some unaffected relatives who may be non-manifesting gene carriers. Our hypothesis was that a subset of unaffected relatives with abnormal spatial acuity would have associated structural abnormalities. Twenty-eight unaffected relatives of patients with familial cervical dystonia, 24 relatives of patients with sporadic cervical dystonia and 27 control subjects were recruited. Spatial discrimination thresholds (SDTs) were determined using a grating orientation task. High-resolution magnetic resonance imaging (MRI) images (1.5 T) were analysed using voxel-based morphometry. Unaffected familial relatives with abnormal SDTs had reduced caudate grey matter volume (GMV) bilaterally relative to those with normal SDTs (right Z = 3.45, left Z = 3.81), where there was a negative correlation between SDTs and GMV (r = -0.76, r(2) = 0.58, p < 0.0001). Familial relatives also had bilateral sensory cortical expansion relative to unrelated controls (right Z = 4.02, left Z = 3.79). Unaffected relatives of patients with sporadic cervical dystonia who had abnormal SDTs had reduced putaminal GMV bilaterally compared with those with normal SDTs (right Z = 3.96, left Z = 3.45). Sensory abnormalities in some unaffected relatives correlate with a striatal substrate and may be a marker of genetic susceptibility in these individuals. Further investigation of grey matter changes as a candidate endophenotype may assist future genetic studies of dystonia.

摘要

成人起病的原发性扭转性肌张力障碍(AOPTD)中已描述了结构性灰质异常。在家族性和散发性AOPTD以及一些可能是未表现出症状的基因携带者的未受影响亲属中发现了空间辨别阈值改变。我们的假设是,一部分空间敏锐度异常的未受影响亲属会有相关的结构异常。招募了28名家族性颈部肌张力障碍患者的未受影响亲属、24名散发性颈部肌张力障碍患者的亲属和27名对照受试者。使用光栅定向任务确定空间辨别阈值(SDT)。使用基于体素的形态学方法分析高分辨率磁共振成像(MRI)图像(1.5T)。与SDT正常的未受影响家族亲属相比,SDT异常的未受影响家族亲属双侧尾状核灰质体积(GMV)减少(右侧Z = 3.45,左侧Z = 3.81),其中SDT与GMV之间存在负相关(r = -0.76,r² = 0.58,p < 0.0001)。家族亲属相对于无关对照也有双侧感觉皮层扩张(右侧Z = 4.02,左侧Z = 3.79)。与SDT正常的散发性颈部肌张力障碍患者的未受影响亲属相比,SDT异常的未受影响亲属双侧壳核GMV减少(右侧Z = 3.96,左侧Z = 3.45)。一些未受影响亲属的感觉异常与纹状体基质相关,可能是这些个体遗传易感性的标志物。作为候选内表型对灰质变化进行进一步研究可能有助于未来肌张力障碍的遗传学研究。

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