Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne NE4 5PL, UK.
School of Biomedical, Nutritional and Sport Sciences, Newcastle University, Newcastle Upon Tyne NE1 7RU, UK.
Sensors (Basel). 2021 Jan 26;21(3):813. doi: 10.3390/s21030813.
Laboratory-based gait assessments are indicative of clinical outcomes (e.g., disease identification). Real-world gait may be more sensitive to clinical outcomes, as impairments may be exaggerated in complex environments. This study aims to investigate how different environments (e.g., lab, real world) impact gait. Different walking bout lengths in the real world will be considered proxy measures of context. Data collected in different dementia disease subtypes will be analysed as disease-specific gait impairments are reported between these groups. Thirty-two people with cognitive impairment due to Alzheimer's disease (AD), 28 due to dementia with Lewy bodies (DLB) and 25 controls were recruited. Participants wore a tri-axial accelerometer for six 10 m walks in lab settings, and continuously for seven days in the real world. Fourteen gait characteristics across five domains were measured (i.e., pace, variability, rhythm, asymmetry, postural control). In the lab, the DLB group showed greater step length variability ( = 0.008) compared to AD. Both subtypes demonstrated significant gait impairments ( < 0.01) compared to controls. In the real world, only very short walking bouts (<10 s) demonstrated different gait impairments between subtypes. The context where walking occurs impacts signatures of gait impairment in dementia subtypes. To develop real-world gait assessment as a clinical tool, algorithms and metrics must accommodate for changes in context.
基于实验室的步态评估可用于预测临床结果(例如,疾病诊断)。现实世界中的步态可能对临床结果更敏感,因为在复杂环境中,损伤可能会被夸大。本研究旨在探讨不同环境(例如实验室、现实世界)如何影响步态。现实世界中不同的步行段长度将被视为环境的替代指标。将对不同痴呆症亚型的数据进行分析,因为这些组之间报告了特定于疾病的步态障碍。招募了 32 名因阿尔茨海默病(AD)导致认知障碍的人,28 名因路易体痴呆症(DLB)导致认知障碍的人和 25 名对照者。参与者在实验室环境中佩戴三轴加速度计进行了六次 10 米步行,在现实世界中连续佩戴了七天。在五个领域中测量了 14 项步态特征(即步速、变异性、节律、不对称性、姿势控制)。在实验室中,与 AD 相比,DLB 组的步长变异性更大( = 0.008)。与对照组相比,两种亚型均表现出明显的步态障碍( < 0.01)。在现实世界中,只有非常短的步行段(<10 秒)在亚型之间显示出不同的步态障碍。行走发生的环境会影响痴呆症亚型的步态障碍特征。为了将现实世界中的步态评估作为一种临床工具,算法和指标必须适应环境变化。