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解析脊髓性肌萎缩症与延髓性肌萎缩症的平衡障碍。

Disentangling balance impairments in spinal and bulbar muscular atrophy.

机构信息

Department of Neurology, University of Athens, Eginition Hospital, Athens, Greece.

Department of Neurology, University of Athens, Eginition Hospital, Athens, Greece.

出版信息

Neurosci Lett. 2019 Jul 13;705:94-98. doi: 10.1016/j.neulet.2019.04.044. Epub 2019 Apr 23.

DOI:10.1016/j.neulet.2019.04.044
PMID:31026532
Abstract

Spinal and bulbar muscular atrophy (Kennedy's disease) has been associated with balance dysfunction and falls. However, postural control has not been studied quantitatively. Here, we quantified upright stance and aimed to disentangle the role of vestibular, proprioceptive and oculomotor deficits. Static balance was assessed in Kennedy patients (n = 7) during quiet stance on a force platform under different visual and proprioceptive feedback conditions. Vestibular function was assessed with the video head impulse test. Sural nerve neurography was employed to evaluate the severity of peripheral neuropathy. Also, horizontal saccades were recorded and quantified by the main sequence relationship. Posturographic analyses revealed significantly increased body sway, more pronounced in conditions with closed eyes, which was also reflected in the calculated Romberg indices. Horizontal vestibulo-ocular reflex gains were normal, i.e. > 0.75. In contrast, compound sensory nerve action potentials were markedly decreased in all patients (mean = 2.4 μV). Two patients showed slow saccades with increased exponential main sequence constants. We conclude that Kennedy patients exhibit severe deficits in quiet stance. Postural instability is greatest in conditions of absent vision with reduced proprioception being the main determinant of unsteadiness. Some patients show slowed saccadic eye movements suggesting a nuclear abducens neuronopathy.

摘要

脊髓延髓肌萎缩症(肯尼迪病)与平衡功能障碍和跌倒有关。然而,尚未对姿势控制进行定量研究。在这里,我们定量了直立姿势,并旨在阐明前庭、本体感觉和眼动缺陷的作用。在力平台上的安静站立期间,通过不同的视觉和本体感觉反馈条件,评估了肯尼迪病患者(n=7)的静态平衡。使用视频头脉冲测试评估前庭功能。通过坐骨神经神经图评估周围神经病变的严重程度。还记录并通过主序列关系量化了水平扫视。姿势图分析显示身体摆动明显增加,闭眼时更为明显,这也反映在计算出的 Romberg 指数中。水平前庭眼反射增益正常,即>0.75。相比之下,所有患者的复合感觉神经动作电位均明显降低(平均=2.4μV)。两名患者表现出扫视缓慢,指数主序列常数增加。我们得出结论,肯尼迪病患者在安静站立时表现出严重的缺陷。在没有视觉的情况下,姿势不稳定最大,本体感觉降低是不稳定的主要决定因素。一些患者表现出扫视缓慢的眼球运动,提示核性展神经神经元病。

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