Using Smartphones and Machine Learning to Quantify Parkinson Disease Severity

医学 步态 物理医学与康复 结构效度 评定量表 帕金森病 物理疗法 相关性 疾病严重程度 平衡(能力) 智能手机应用 金标准(测试) 疾病 心理学 心理测量学 内科学 临床心理学 发展心理学 计算机科学 多媒体 数学 几何学
作者
Andong Zhan,Srihari Mohan,Christopher G. Tarolli,Ruth B. Schneider,Jamie Adams,Saloni Sharma,Molly J. Elson,Kelsey L. Spear,Alistair M. Glidden,Max A. Little,Andreas Terzis,E. Ray Dorsey,Suchi Saria
出处
期刊:JAMA Neurology [American Medical Association]
卷期号:75 (7): 876-876 被引量:352
标识
DOI:10.1001/jamaneurol.2018.0809
摘要

Importance

Current Parkinson disease (PD) measures are subjective, rater-dependent, and assessed in clinic. Smartphones can measure PD features, yet no smartphone-derived rating score exists to assess motor symptom severity in real-world settings.

Objectives

To develop an objective measure of PD severity and test construct validity by evaluating the ability of the measure to capture intraday symptom fluctuations, correlate with current standard PD outcome measures, and respond to dopaminergic therapy.

Design, Setting, and Participants

This observational study assessed individuals with PD who remotely completed 5 tasks (voice, finger tapping, gait, balance, and reaction time) on the smartphone application. We used a novel machine-learning–based approach to generate a mobile Parkinson disease score (mPDS) that objectively weighs features derived from each smartphone activity (eg, stride length from the gait activity) and is scaled from 0 to 100 (where higher scores indicate greater severity). Individuals with and without PD additionally completed standard in-person assessments of PD with smartphone assessments during a period of 6 months.

Main Outcomes and Measures

Ability of the mPDS to detect intraday symptom fluctuations, the correlation between the mPDS and standard measures, and the ability of the mPDS to respond to dopaminergic medication.

Results

The mPDS was derived from 6148 smartphone activity assessments from 129 individuals (mean [SD] age, 58.7 [8.6] years; 56 [43.4%] women). Gait features contributed most to the total mPDS (33.4%). In addition, 23 individuals with PD (mean [SD] age, 64.6 [11.5] years; 11 [48%] women) and 17 without PD (mean [SD] age 54.2 [16.5] years; 12 [71%] women) completed in-clinic assessments. The mPDS detected symptom fluctuations with a mean (SD) intraday change of 13.9 (10.3) points on a scale of 0 to 100. The measure correlated well with the Movement Disorder Society Unified Parkinson Disease's Rating Scale total (r = 0.81;P < .001) and part III only (r = 0.88;P < .001), the Timed Up and Go assessment (r = 0.72;P = .002), and the Hoehn and Yahr stage (r = 0.91;P < .001). The mPDS improved by a mean (SD) of 16.3 (5.6) points in response to dopaminergic therapy.

Conclusions and Relevance

Using a novel machine-learning approach, we created and demonstrated construct validity of an objective PD severity score derived from smartphone assessments. This score complements standard PD measures by providing frequent, objective, real-world assessments that could enhance clinical care and evaluation of novel therapeutics.
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