Moving beyond monitoring: wearable technology (PKG) for the diagnosis of Parkinson's disease.

IF 2.6 Q3 CLINICAL NEUROLOGY
BMJ Neurology Open Pub Date : 2026-09-03 eCollection Date: 2026-01-01 DOI:10.1136/bmjno-2026-001689
Michael William Hayes, Niroshan Jeyakumar, James Burrell
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引用次数: 0

Abstract

Background: The use of wearable technology results in objective and reliable monitoring of motor activity in Parkinson's disease (PD) but its utility as a diagnostic aid has not been assessed.

Objectives: To assess whether a Personal KinetiGraph (PKG) performed at baseline and again following a long-form levodopa (LD) challenge (increasing to 300 mg daily over a minimum of 6 weeks) is a useful discriminator in those with parkinsonism but diagnostic uncertainty.

Methods: Over a 10-year period, 26 patients with parkinsonism in whom there was diagnostic uncertainty due to clinical complexity or conflicting evidence were tested with a PKG, recording bradykinesia and tremor before and after formalised treatment with LD. Patients were followed for a median of 46.5 months (mean 49.8) to establish a 'final' clinical diagnosis.

Results: Of the 15/26 diagnostically uncertain patients with a 'final' diagnosis of PD, the PKG demonstrated bradykinesia (mean bradykinesia score ≥25) at baseline in 14/15; in 12/15, bradykinesia improved with LD and, when present, tremor was similarly reduced. In the 11/26 patients who had a final diagnosis other than PD, the PKG recorded bradykinesia in 3/11 with improved bradykinesia and reduced tremor in only 1/11. PKG-defined bradykinesia coupled with LD responsiveness was 88% sensitive (95% CI 57% to 98%) and 89% specific (95% CI 52% to 99%) for a 'final' PD diagnosis in this select group. Additionally, PKG-defined tremor and LD responsiveness had a sensitivity of 85% (95% CI 55% to 98%) and specificity of 89% (95% CI 52% to 99%).

Conclusion: PKG-defined bradykinesia and tremor coupled with LD responsiveness appear to be predictive of an eventual PD diagnosis in diagnostically challenging cases. Larger studies are required to verify these conclusions.

超越监测:可穿戴技术(PKG)用于帕金森病的诊断。
背景:可穿戴技术的使用可以客观可靠地监测帕金森病(PD)患者的运动活动,但其作为诊断辅助手段的效用尚未得到评估。目的:评估个人KinetiGraph (PKG)在基线和长期左旋多巴(LD)刺激(至少6周增加到每天300毫克)后是否对帕金森病诊断不确定的患者有用。方法:在10年的时间里,26例由于临床复杂性或相互矛盾的证据而诊断不确定的帕金森病患者用PKG进行了测试,记录了LD正式治疗前后的运动迟缓和震颤。患者随访中位数为46.5个月(平均49.8个月),以建立“最终”临床诊断。结果:在“最终”诊断为PD的15/26例诊断不确定的患者中,14/15例PKG在基线时表现为运动迟缓(平均运动迟缓评分≥25);在12/15中,运动迟缓随着LD而改善,当存在时,震颤也同样减少。在11/26最终诊断为非PD的患者中,PKG记录了3/11的运动迟缓,只有1/11的运动迟缓改善和震颤减轻。在这个选择的组中,pkg定义的运动迟缓合并LD反应性的“最终”PD诊断敏感性为88% (95% CI 57%至98%),特异性为89% (95% CI 52%至99%)。此外,pkg定义的震颤和LD反应性敏感性为85% (95% CI为55%至98%),特异性为89% (95% CI为52%至99%)。结论:在诊断困难的病例中,pkg定义的运动迟缓和震颤加上LD反应性似乎可以预测最终的PD诊断。需要更大规模的研究来验证这些结论。
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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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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