自动真实世界坐立转换视频分析可预测帕金森病的严重程度

Q1 Computer Science Digital Biomarkers Pub Date : 2023-08-14 eCollection Date: 2023-01-01 DOI:10.1159/000530953
Catherine Morgan, Alessandro Masullo, Majid Mirmehdi, Hanna Kristiina Isotalus, Ferdian Jovan, Ryan McConville, Emma L Tonkin, Alan Whone, Ian Craddock
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摘要

简介:技术有望跟踪帕金森病(PD)的病情发展和对神经保护疗法的反应。坐立转换(STS)是一个经常发生的过程,对帕金森病患者非常重要。本研究旨在展示一种自动方法,利用真实世界的自由生活数据集量化坐立转换的持续时间和速度,并研究结果的临床相关性,包括当患者停用帕金森病药物时,坐立转换参数是否会发生变化:方法: 在自然环境中,收集了 24 名参与者 5 天内两人一组的 85 小时视频数据。从视频数据中提取骨骼关节;估算头部轨迹并用于估算持续时间和速度的 STS 参数:结果:平均每人每小时看到 3.14 次 STS 过渡。自动 STS 持续时间与手动 STS 持续时间之间存在显著相关性(Pearson rho - 0.419,p = 0.042),自动 STS 速度与手动 STS 持续时间之间也存在显著相关性(Pearson rho - 0.780,p < 0.001)。金标准临床评分量表得分与STS持续时间和STS速度之间存在显著的强相关性;但在参与者手持物品时的STS转换中则未发现这些相关性。在组群水平上,对照组和帕金森病患者服用 ON 药物时的 STS 持续时间(U = 6,263, p = 0.018)和速度(U = 9,965, p < 0.001)之间存在显著差异。在个体水平上,只有两名帕金森氏症患者在停药后STS明显变慢;在个体水平上,停药并没有显著改变任何参与者的STS持续时间:我们展示了一种自动量化和生态验证两个 STS 参数的新方法,这两个参数与衡量帕金森病疾病严重程度的黄金标准临床工具相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Automated Real-World Video Analysis of Sit-to-Stand Transitions Predicts Parkinson's Disease Severity.

Introduction: Technology holds the potential to track disease progression and response to neuroprotective therapies in Parkinson's disease (PD). The sit-to-stand (STS) transition is a frequently occurring event which is important to people with PD. The aim of this study was to demonstrate an automatic approach to quantify STS duration and speed using a real-world free-living dataset and look at clinical correlations of the outcomes, including whether STS parameters change when someone withholds PD medications.

Methods: Eighty-five hours of video data were collected from 24 participants staying in pairs for 5-day periods in a naturalistic setting. Skeleton joints were extracted from the video data; the head trajectory was estimated and used to estimate the STS parameters of duration and speed.

Results: 3.14 STS transitions were seen per hour per person on average. Significant correlations were seen between automatic and manual STS duration (Pearson rho - 0.419, p = 0.042) and between automatic STS speed and manual STS duration (Pearson rho - 0.780, p < 0.001). Significant and strong correlations were seen between the gold-standard clinical rating scale scores and both STS duration and STS speed; these correlations were not seen in the STS transitions when the participants were carrying something in their hand(s). Significant differences were seen at the cohort level between control and PD participants' ON medications' STS duration (U = 6,263, p = 0.018) and speed (U = 9,965, p < 0.001). At an individual level, only two participants with PD became significantly slower to STS when they were OFF medications; withholding medications did not significantly change STS duration at an individual level in any participant.

Conclusion: We demonstrate a novel approach to automatically quantify and ecologically validate two STS parameters which correlate with gold-standard clinical tools measuring disease severity in PD.

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来源期刊
Digital Biomarkers
Digital Biomarkers Medicine-Medicine (miscellaneous)
CiteScore
10.60
自引率
0.00%
发文量
12
审稿时长
23 weeks
期刊最新文献
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