Tian Hao, Yasunori Yamada, Jeffrey L. Rogers, Kaoru Shinakwa, M. Nemoto, K. Nemoto, T. Arai
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引用次数: 1
摘要
TUG (Timed Up and Go)测试是一种常见的临床终点,但由于需要在训练有素的评估人员(通常是临床医生)在场的情况下进行,因此受到限制。在这里,我们提出了一个基于机器学习的传感器无关的自动化管道,通过使用常用的可穿戴传感器捕获的日常步行来预测TUG分数,通过生成被动和连续的移动性生物标志物流,而无需进行脚本化的TUG测试。我们对来自三个队列数据集的303名参与者的数据进行了验证,每个队列数据集的主要关注人群不同,包括健康老年人、帕金森病患者和轻度认知障碍或痴呆患者。除了TUG得分外,这三个数据集还包括从不同的可穿戴传感器收集的步行数据,分别是下背加速度计、腕带加速度计和鞋底压力步态传感器。我们对来自所有队列的参与者进行的留一受试者验证表明,随机森林预测模型的准确度为1.7±1.7s(平均绝对误差±标准差),在最小可检测变化范围内(±3s)的预测精度为84.8%,具有合理的跨队列通化性。通过对使用三种常用可穿戴传感器收集的数据进行验证,我们证明了我们提出的管道利用异构输入从步行数据中预测TUG分数的能力,这表明通过利用自由生活场景中自然发生的步行来生成连续的TUG预测流作为移动性的新型数字生物标志物的可行性。我们的研究还表明,对于某些队列(例如,帕金森病人群),应用队列特定模型而不是使用混合队列训练的模型可能会进一步提高性能。
The Timed Up and Go (TUG) test is a common clinical endpoint, but is limited by the need to conduct it in the presence of a trained evaluator, usually a clinician. Herein, we propose a sensor-agnostic automated pipeline based on machine learning to predict TUG scores using day-to-day walks captured using commonly used wearable sensors by generating a passive and continual stream of mobility biomarkers without the need of conducting scripted TUG tests. We validated our pipeline against data from 303 participants in three cohort datasets, each with a different primary focus population of healthy elderly adults, Parkinson’s disease patients, and patients with mild cognitive impairment or dementia. In addition to TUG scores, the three datasets include walking data collected from different wearable sensors, i.e., a lower-back-worn accelerometer, wrist-worn accelerometer, and in-sole pressure gait sensor, respectively. Our leave-one-subject-out validation using participants from all cohorts showed that a random-forest predictive model achieved an accuracy of 1.7 ± 1.7s (mean absolute error ± standard deviation) and 84.8% predictions within the minimal detectable change (± 3s) with reasonable generalization across cohorts. Through the validation on data collected using he three types of commonly used wearable sensors, we demonstrated the ability of our proposed pipeline to leverage heterogeneous inputs for predicting TUG scores from walking data, suggesting the feasibility to generate a continual stream of TUG predictions as a novel digital biomarker of mobility by leveraging naturally occurring walks in free-living scenario. Our investigation also suggests that, for certain cohorts (e.g., Parkinson’s disease population), applying a cohort-specific model instead of using a model trained with mixed cohorts might further improve performance.