TY - JOUR
T1 - Decomposition of Reaching Movements Enables Detection and Measurement of Ataxia
AU - Oubre, Brandon
AU - Daneault, Jean Francois
AU - Whritenour, Kallie
AU - Khan, Nergis C.
AU - Stephen, Christopher D.
AU - Schmahmann, Jeremy D.
AU - Lee, Sunghoon Ivan
AU - Gupta, Anoopum S.
N1 - Funding Information:
Ataxia-Telangiectasia Children’s Project, Biogen Inc., APDM Wearable Technologies, and NSF grant 1755687 as part of the NSF/NIH Smart and Connected Health program.
Funding Information:
The authors would like to thank Mary Donovan and Winnie Ching for data collection; Pavan Vaswani for creating the experimental stimuli; Albert Hung and Anne-Marie Wills for participant recruitment; and the Ataxia-Telangiectasia Children’s Project, Biogen Inc., APDM Wearable Technologies, and NSF grant 1755687 (NSF/NIH Smart and Connected Health) for study funding.
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Technologies that enable frequent, objective, and precise measurement of ataxia severity would benefit clinical trials by lowering participation barriers and improving the ability to measure disease state and change. We hypothesized that analyzing characteristics of sub-second movement profiles obtained during a reaching task would be useful for objectively quantifying motor characteristics of ataxia. Participants with ataxia (N=88), participants with parkinsonism (N=44), and healthy controls (N=34) performed a computer tablet version of the finger-to-nose test while wearing inertial sensors on their wrists. Data features designed to capture signs of ataxia were extracted from participants’ decomposed wrist velocity time-series. A machine learning regression model was trained to estimate overall ataxia severity, as measured by the Brief Ataxia Rating Scale (BARS). Classification models were trained to distinguish between ataxia participants and controls and between ataxia and parkinsonism phenotypes. Movement decomposition revealed expected and novel characteristics of the ataxia phenotype. The distance, speed, duration, morphology, and temporal relationships of decomposed movements exhibited strong relationships with disease severity. The regression model estimated BARS with a root mean square error of 3.6 points, r2 = 0.69, and moderate-to-excellent reliability. Classification models distinguished between ataxia participants and controls and ataxia and parkinsonism phenotypes with areas under the receiver-operating curve of 0.96 and 0.89, respectively. Movement decomposition captures core features of ataxia and may be useful for objective, precise, and frequent assessment of ataxia in home and clinic environments.
AB - Technologies that enable frequent, objective, and precise measurement of ataxia severity would benefit clinical trials by lowering participation barriers and improving the ability to measure disease state and change. We hypothesized that analyzing characteristics of sub-second movement profiles obtained during a reaching task would be useful for objectively quantifying motor characteristics of ataxia. Participants with ataxia (N=88), participants with parkinsonism (N=44), and healthy controls (N=34) performed a computer tablet version of the finger-to-nose test while wearing inertial sensors on their wrists. Data features designed to capture signs of ataxia were extracted from participants’ decomposed wrist velocity time-series. A machine learning regression model was trained to estimate overall ataxia severity, as measured by the Brief Ataxia Rating Scale (BARS). Classification models were trained to distinguish between ataxia participants and controls and between ataxia and parkinsonism phenotypes. Movement decomposition revealed expected and novel characteristics of the ataxia phenotype. The distance, speed, duration, morphology, and temporal relationships of decomposed movements exhibited strong relationships with disease severity. The regression model estimated BARS with a root mean square error of 3.6 points, r2 = 0.69, and moderate-to-excellent reliability. Classification models distinguished between ataxia participants and controls and ataxia and parkinsonism phenotypes with areas under the receiver-operating curve of 0.96 and 0.89, respectively. Movement decomposition captures core features of ataxia and may be useful for objective, precise, and frequent assessment of ataxia in home and clinic environments.
KW - Ataxia
KW - Brief Ataxia Rating Scale
KW - Machine learning
KW - Movement decomposition
KW - Wearable electronic devices
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U2 - 10.1007/s12311-021-01247-6
DO - 10.1007/s12311-021-01247-6
M3 - Article
C2 - 33651372
AN - SCOPUS:85102079101
SN - 1473-4222
VL - 20
SP - 811
EP - 822
JO - Cerebellum
JF - Cerebellum
IS - 6
ER -