Quantitative Digitography Measures Motor Symptoms and Disease Progression in Parkinson's Disease

被引:9
作者
Wilkins, Kevin B. [1 ]
Petrucci, Matthew N. [1 ]
Kehnemouyi, Yasmine [1 ]
Velisar, Anca [1 ,2 ]
Han, Katie [1 ]
Orthlieb, Gerrit [1 ]
Trager, Megan H. [1 ,3 ]
O'Day, Johanna J. [1 ,4 ]
Aditham, Sudeep [1 ]
Bronte-Stewart, Helen [1 ,5 ]
机构
[1] Stanford Univ, Dept Neurol & Neurol Sci, Sch Med, Stanford, CA USA
[2] Smith Kettlewell Eye Res Inst, 2232 Webster St, San Francisco, CA 94115 USA
[3] Columbia Univ Coll Phys & Surg, 630 W 168th St, New York, NY 10032 USA
[4] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Neurosurg, Sch Med, Stanford, CA 94305 USA
关键词
Alternating finger tapping; cardinal motor signs; freezing of gait; keyboard; Parkinson's disease; phenotype; remote measurement; rigidity; Unified Parkinson's Disease Rating Scale; wearables; EARLY-STAGE; FINE MOTOR; GAIT; LIMB; BRADYKINESIA;
D O I
10.3233/JPD-223264
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Assessment of motor signs in Parkinson's disease (PD) requires an in-person examination. However, 50% of people with PD do not have access to a neurologist. Wearable sensors can provide remote measures of some motor signs but require continuous monitoring for several days. A major unmet need is reliable metrics of all cardinal motor signs, including rigidity, from a simple short active task that can be performed remotely or in the clinic. Objective: Investigate whether thirty seconds of repetitive alternating finger tapping (RAFT) on a portable quantitative digitography (QDG) device, which measures amplitude and timing, produces reliable metrics of all cardinal motor signs in PD. Methods: Ninety-six individuals with PD and forty-two healthy controls performed a thirty-second QDG-RAFT task and clinical motor assessment. Eighteen individuals were followed longitudinally with repeated assessments for an average of three years and up to six years. Results: QDG-RAFT metrics showed differences between PD and controls and provided correlated metrics for total motor disability (MDS-UPDRS III) and for rigidity, bradykinesia, tremor, gait impairment, and freezing of gait (FOG). Additionally, QDG-RAFT tracked disease progression over several years off therapy and showed differences between akinetic-rigid and tremor-dominant phenotypes, as well as people with and without FOG. Conclusion: QDG is a reliable technology, which could be used in the clinic or remotely. This could improve access to care, allow complex remote disease management based on data received in real time, and accurate monitoring of disease progression over time in PD. QDG-RAFT also provides the comprehensive motor metrics needed for therapeutic trials.
引用
收藏
页码:1979 / 1990
页数:12
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