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在早期多发性硬化症患者中,尽管其行走功能正常,但在水平转头行走时会受到损害。

Walking With Horizontal Head Turns Is Impaired in Persons With Early-Stage Multiple Sclerosis Showing Normal Locomotion.

作者信息

Carpinella Ilaria, Gervasoni Elisa, Anastasi Denise, Di Giovanni Rachele, Tacchino Andrea, Brichetto Giampaolo, Confalonieri Paolo, Solaro Claudio, Rovaris Marco, Ferrarin Maurizio, Cattaneo Davide

机构信息

IRCSS Fondazione Don Carlo Gnocchi, Milan, Italy.

Centro di Recupero e Rieducazione Funzionale (CRRF) Mons. Luigi Novarese, Moncrivello, Italy.

出版信息

Front Neurol. 2022 Jan 28;12:821640. doi: 10.3389/fneur.2021.821640. eCollection 2021.

Abstract

BACKGROUND

Turning the head while walking (an action often required during daily living) is particularly challenging to maintain balance. It can therefore potentially reveal subtle impairments in early-stage people with multiple sclerosis who still show normal locomotion (NW-PwMS). This would help in identifying those subjects who can benefit from early preventive exercise aimed at slowing the MS-related functional decline.

OBJECTIVES

To analyze if the assessment of walking with horizontal head turns (WHHT) through inertial sensors can discriminate between healthy subjects (HS) and NW-PwMS and between NW-PwMS subgroups. To assess if the discriminant ability of the instrumented WHHT is higher compared to clinical scores. To assess the concurrent validity of the sensor-based metrics.

METHODS

In this multicenter study, 40 HS and 59 NW-PwMS [Expanded Disability Status Scale (EDSS) ≤ 2.5, disease duration ≤ 5 years] were tested. Participants executed Item-6 of the Fullerton Advanced Balance scale-short (FAB-s) wearing three inertial sensors on the trunk and ankles. The item required to horizontally turn the head at a beat of the metronome (100 bpm) while walking. Signals of the sensors were processed to compute spatiotemporal, regularity, symmetry, dynamic stability, and trunk sway metrics descriptive of WHHT.

RESULTS

Mediolateral regularity, anteroposterior symmetry, and mediolateral stability were reduced in NW-PwMS vs. HS ( ≤ 0.001), and showed moderate discriminant ability (area under the receiver operator characteristic curve [AUC]: 0.71-0.73). AP symmetry and ML stability were reduced ( ≤ 0.026) in EDSS: 2-2.5 vs. EDSS: 0-1.5 subgroup (AUC: 0.69-0.70). The number of NW-PwMS showing at least one abnormal instrumented metric (68%) was larger ( ≤ 0.002) than the number of participants showing abnormal FAB-s-Item6 (32%) and FAB-s clinical scores (39%). EDSS: 2-2.5 subgroup included more individuals showing abnormal instrumented metrics (86%) compared to EDSS: 0-1.5 subgroup (57%). The instrumented metrics significantly correlated with FAB-s-Item6 and FAB-s scores (|Spearman's | ≥ 0.37, < 0.001), thus demonstrating their concurrent validity.

CONCLUSION

The instrumented assessment of WHHT provided valid objective metrics that discriminated, with higher sensitivity than clinical scores, between HS and NW-PwMS and between EDSS subgroups. The method is a promising tool to complement clinical evaluation, and reveal subclinical impairments in persons who can benefit from early preventive rehabilitative interventions.

摘要

背景

行走时转头(日常生活中经常需要的动作)对维持平衡特别具有挑战性。因此,它可能会揭示出早期多发性硬化症患者(仍表现出正常运动能力,即NW-PwMS)的细微损伤。这将有助于识别那些能够从旨在减缓与MS相关功能衰退的早期预防性运动中受益的受试者。

目的

分析通过惯性传感器对水平转头行走(WHHT)进行评估是否能够区分健康受试者(HS)和NW-PwMS,以及区分NW-PwMS亚组。评估仪器化WHHT的判别能力是否高于临床评分。评估基于传感器的指标的同时效度。

方法

在这项多中心研究中,对40名HS和59名NW-PwMS(扩展残疾状态量表[EDSS]≤2.5,病程≤5年)进行了测试。参与者在躯干和脚踝上佩戴三个惯性传感器,执行富勒顿高级平衡量表简版(FAB-s)的第6项。该项目要求在行走时随着节拍器的节拍(100次/分钟)水平转头。对传感器信号进行处理,以计算描述WHHT的时空、规律性、对称性、动态稳定性和躯干摆动指标。

结果

与HS相比,NW-PwMS的内外侧规律性、前后对称性和内外侧稳定性降低(≤0.001),并显示出中等判别能力(受试者工作特征曲线下面积[AUC]:0.71-0.73)。EDSS为2-2.5的亚组与EDSS为0-1.5的亚组相比,前后对称性和内外侧稳定性降低(≤0.026)(AUC:0.69-0.70)。显示至少一项仪器化指标异常的NW-PwMS数量(68%)比显示FAB-s第6项异常(32%)和FAB-s临床评分异常(39%)的参与者数量更多(≤0.002)。与EDSS为0-1.5的亚组(57%)相比,EDSS为2-2.5的亚组中有更多个体显示仪器化指标异常(86%)。仪器化指标与FAB-s第6项和FAB-s评分显著相关(|斯皮尔曼相关性系数|≥0.37,P<0.001),从而证明了它们的同时效度。

结论

对WHHT进行仪器化评估提供了有效的客观指标,能够以高于临床评分的灵敏度区分HS和NW-PwMS以及EDSS亚组。该方法是一种很有前景的工具,可补充临床评估,并揭示能够从早期预防性康复干预中受益的人群的亚临床损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac7/8833075/b57a6fa75fce/fneur-12-821640-g0001.jpg

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