IEEE J Biomed Health Inform. 2020 May;24(5):1490-1499. doi: 10.1109/JBHI.2019.2937574. Epub 2019 Aug 26.
Hereditary spastic paraplegias (HSP) represents a group of orphan neurodegenerative diseases with gait disturbance as the predominant clinical feature. Due to its rarity, research within this field is still limited. Aside from clinical analysis using established scales, gait analysis has been employed to enhance the understanding of the mechanisms behind the disease. However, state of the art gait analysis systems are often large, immobile and expensive. To overcome these limitations, this paper presents the first clinically relevant mobile gait analysis system for HSP patients. We propose an unsupervised model based on local cyclicity estimation and hierarchical hidden Markov models (LCE-hHMM). The system provides stride time, swing time, stance time, swing duration and cadence. These parameters are validated against a GAITRite system and manual sensor data labelling using a total of 24 patients within 2 separate studies. The proposed system achieves a stride time error of -0.00 ± 0.09 s (correlation coefficient, r = 1.00) and a swing duration error of -0.67 ± 3.27 % (correlation coefficient, r = 0.93) with respect to the GAITRite system. We show that these parameters are also correlated to the clinical spastic paraplegia rating scale (SPRS) in a similar manner to other state of the art gait analysis systems, as well as to supervised and general versions of the proposed model. Finally, we show a proof of concept for this system to be used to analyse alterations in the gait of individual patients. Thus, with further clinical studies, due to its automated approach and mobility, this system could be used to determine treatment effects in future clinical trials.
遗传性痉挛性截瘫 (HSP) 是一组孤儿神经退行性疾病,以步态障碍为主要临床特征。由于其罕见性,该领域的研究仍然有限。除了使用既定量表进行临床分析外,步态分析也被用于增强对疾病背后机制的理解。然而,最先进的步态分析系统通常体积大、固定且昂贵。为了克服这些限制,本文提出了第一个针对 HSP 患者的临床相关移动步态分析系统。我们提出了一种基于局部周期性估计和分层隐马尔可夫模型 (LCE-hHMM) 的无监督模型。该系统提供步长时间、摆动时间、站立时间、摆动持续时间和步频。这些参数使用总共 24 名患者在 2 项独立研究中与 GAITRite 系统和手动传感器数据标记进行了验证。与 GAITRite 系统相比,所提出的系统的步长时间误差为-0.00 ± 0.09 s(相关系数,r = 1.00),摆动持续时间误差为-0.67 ± 3.27%(相关系数,r = 0.93)。我们表明,这些参数与临床痉挛性截瘫评分量表 (SPRS) 的相关性与其他最先进的步态分析系统以及经过监督和一般化的模型版本相似。最后,我们展示了该系统用于分析个别患者步态变化的概念验证。因此,通过进一步的临床研究,由于其自动化方法和移动性,该系统可用于确定未来临床试验中的治疗效果。