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Physiol Meas. 2019 Sep 30;40(9):095003. doi: 10.1088/1361-6579/ab4023.
2
Proposal of a new conceptual gait model for patients with Parkinson's disease based on factor analysis.基于因子分析的帕金森病患者新概念步态模型的提出。
Biomed Eng Online. 2019 Jun 3;18(1):70. doi: 10.1186/s12938-019-0689-3.
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Gait impairments in Parkinson's disease.帕金森病的步态障碍。
Lancet Neurol. 2019 Jul;18(7):697-708. doi: 10.1016/S1474-4422(19)30044-4. Epub 2019 Apr 8.
4
A roadmap for implementation of patient-centered digital outcome measures in Parkinson's disease obtained using mobile health technologies.利用移动健康技术实施以患者为中心的帕金森病数字结局测量的路线图。
Mov Disord. 2019 May;34(5):657-663. doi: 10.1002/mds.27671. Epub 2019 Mar 22.
5
Smartphone motor testing to distinguish idiopathic REM sleep behavior disorder, controls, and PD.智能手机运动测试可用于区分特发性 REM 睡眠行为障碍、对照组和 PD。
Neurology. 2018 Oct 16;91(16):e1528-e1538. doi: 10.1212/WNL.0000000000006366. Epub 2018 Sep 19.
6
Evaluation of smartphone-based testing to generate exploratory outcome measures in a phase 1 Parkinson's disease clinical trial.基于智能手机的测试评估在帕金森病 1 期临床试验中生成探索性结局指标。
Mov Disord. 2018 Aug;33(8):1287-1297. doi: 10.1002/mds.27376. Epub 2018 Apr 27.
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Using Smartphones and Machine Learning to Quantify Parkinson Disease Severity: The Mobile Parkinson Disease Score.使用智能手机和机器学习量化帕金森病严重程度:移动帕金森病评分。
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8
Natural turn measures predict recurrent falls in community-dwelling older adults: a longitudinal cohort study.自然转身测量可预测社区居住的老年人反复跌倒:一项纵向队列研究。
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9
Turn Around Freezing: Community-Living Turning Behavior in People with Parkinson's Disease.转身冻结:帕金森病患者在社区生活中的转身行为
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10
Neurological disorders of gait, balance and posture: a sign-based approach.步态、平衡和姿势的神经障碍:基于征象的方法。
Nat Rev Neurol. 2018 Mar;14(3):183-189. doi: 10.1038/nrneurol.2017.178. Epub 2018 Jan 29.

帕金森病日常生活中的移动数字生物标志物。

Digital Biomarkers of Mobility in Parkinson's Disease During Daily Living.

机构信息

Department of Neurology, Oregon Health & Science University, Portland, OR, USA.

Department of Electrical and Computer Engineering, Portland State University, Portland, OR, USA.

出版信息

J Parkinsons Dis. 2020;10(3):1099-1111. doi: 10.3233/JPD-201914.

DOI:10.3233/JPD-201914
PMID:32417795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8128134/
Abstract

BACKGROUND

Identifying digital biomarkers of mobility is important for clinical trials in Parkinson's disease (PD).

OBJECTIVE

To determine which digital outcome measures of mobility discriminate mobility in people with PD from healthy control (HC) subjects over a week of continuous monitoring.

METHODS

We recruited 29 people with PD, and 27 age-matched HC subjects. Subjects were asked to wear three inertial sensors (Opal by APDM) attached to both feet and to the lumbar region, and a subset of subjects also wore two wrist sensors, for a week of continuous monitoring. We derived 43 digital outcome measures of mobility grouped into five domains. An Area Under Curve (AUC) was calculated for each digital outcome measures of mobility, and logistic regression employing a 'best subsets selection strategy' was used to find combinations of measures that discriminated mobility in PD from HC.

RESULTS

Duration of recordings was 66±14 hours in the PD and 59±16 hours in the HC. Out of a total of 43 digital outcome measures of mobility, we found six digital outcome measures of mobility with AUC > 0.80. Turn angle (AUC = 0.89, 95% CI: 0.79-0.97) and swing time variability (AUC = 0.87, 95% CI: 0.75-0.96) were the most discriminative individual measures. Turning measures were most consistently selected via the best subsets strategy to discriminate people with PD from HC, followed by gait variability measures.

CONCLUSION

Clinical studies and clinical practice with digital biomarkers of daily life mobility in PD should include turning and variability measures.

摘要

背景

识别移动的数字生物标志物对于帕金森病(PD)的临床试验很重要。

目的

确定在一周的连续监测中,哪些移动的数字结果衡量标准可以区分 PD 患者和健康对照(HC)受试者的移动能力。

方法

我们招募了 29 名 PD 患者和 27 名年龄匹配的 HC 受试者。要求受试者佩戴三个惯性传感器(APDM 的 Opal),分别附在双脚和腰部,部分受试者还佩戴两个腕部传感器,进行一周的连续监测。我们从五个领域中得出了 43 个移动的数字结果衡量标准。为每个移动的数字结果衡量标准计算了曲线下面积(AUC),并采用“最佳子集选择策略”的逻辑回归来寻找区分 PD 患者和 HC 受试者移动能力的措施组合。

结果

PD 组的记录持续时间为 66±14 小时,HC 组为 59±16 小时。在总共 43 个移动的数字结果衡量标准中,我们发现了六个 AUC>0.80 的数字移动结果衡量标准。转角(AUC=0.89,95%置信区间:0.79-0.97)和摆动时间变异性(AUC=0.87,95%置信区间:0.75-0.96)是最具区分性的个体措施。通过最佳子集策略,转弯测量是最一致地选择来区分 PD 患者和 HC,其次是步态变异性测量。

结论

在 PD 患者的日常生活移动数字生物标志物的临床研究和临床实践中,应包括转弯和变异性测量。