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继发进展型多发性硬化症患者姿势控制受损的神经结构关联

Structural Neural Correlates of Impaired Postural Control in People with Secondary Progressive Multiple Sclerosis.

作者信息

Arpan Ishu, Fling Brett, Powers Katherine, Horak Fay B, Spain Rebecca I

出版信息

Int J MS Care. 2020 May-Jun;22(3):123-128. doi: 10.7224/1537-2073.2019-004. Epub 2019 Aug 29.

Abstract

BACKGROUND

Secondary progressive multiple sclerosis (SPMS) is characterized by worsening of postural control and brain atrophy. However, little is known about postural deficits and their neuroanatomical correlates in this population. We aimed to determine the neuroanatomical correlates of postural deficits in people with SPMS and whether posture control deteriorates concomitantly with the brain and spinal cord atrophy in 2 years in SPMS.

METHODS

This study is a post hoc analysis of data from 27 people with SPMS (mean ± SE age, 58.6 ± 1.1 years). Participants had magnetic resonance imaging (MRI) of the brain and cervical spinal cord followed by sway testing using inertial sensors during standing with eyes open (EO) and eyes closed without (EC) and with (ECC) a cognitive task. Partial correlations investigated relationships between postural control and MRI measures at baseline and 2 years.

RESULTS

At baseline, sway measures were inversely related to cortical thickness and cord cross-sectional area (CSA) during the EO task but only to cord CSA with EC ( < .05). After 2 years, the percentage change in sway amplitude and dispersion during EO tasks significantly related to the percentage decline in cord CSA ( < .01).

CONCLUSIONS

Cortical and spinal cord inputs are essential for regulation of postural control during standing with EO in SPMS. Without visual input, people with SPMS preferentially rely on somatosensory inputs from the spinal cord for maintaining postural control. Postural deficits related to cord atrophy over 2 years, suggesting that postural control may be a surrogate marker of disease progression in people with SPMS.

摘要

背景

继发进展型多发性硬化(SPMS)的特征是姿势控制恶化和脑萎缩。然而,对于该人群的姿势缺陷及其神经解剖学相关性知之甚少。我们旨在确定SPMS患者姿势缺陷的神经解剖学相关性,以及在2年时间里,SPMS患者的姿势控制是否会随着脑和脊髓萎缩而同时恶化。

方法

本研究是对27例SPMS患者(平均±标准误年龄,58.6±1.1岁)的数据进行的事后分析。参与者接受了脑部和颈段脊髓的磁共振成像(MRI)检查,随后在睁眼(EO)站立、闭眼(EC)站立以及闭眼同时进行认知任务(ECC)时,使用惯性传感器进行摇摆测试。偏相关性分析研究了基线和2年时姿势控制与MRI测量值之间的关系。

结果

在基线时,摇摆测量值在EO任务期间与皮质厚度和脊髓横截面积(CSA)呈负相关,但在EC时仅与脊髓CSA呈负相关(P<0.05)。2年后,EO任务期间摇摆幅度和离散度的百分比变化与脊髓CSA的百分比下降显著相关(P<0.01)。

结论

在SPMS患者中,皮质和脊髓输入对于睁眼站立时姿势控制的调节至关重要。在没有视觉输入的情况下,SPMS患者优先依赖来自脊髓的体感输入来维持姿势控制。姿势缺陷与2年内脊髓萎缩相关,提示姿势控制可能是SPMS患者疾病进展的替代标志物。

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