TY - JOUR
T1 - Quantity and quality of gait and turning in people with multiple sclerosis, Parkinson’s disease and matched controls during daily living
AU - Shah, Vrutangkumar V.
AU - McNames, James
AU - Mancini, Martina
AU - Carlson-Kuhta, Patricia
AU - Spain, Rebecca I.
AU - Nutt, John G.
AU - El-Gohary, Mahmoud
AU - Curtze, Carolin
AU - Horak, Fay B.
N1 - Funding Information:
We thank our participants for generously donating their time to participate and Graham Harker for helping with data collection. This study was supported by the National Multiple Sclerosis Society Mentor Fellowship (MB0027), and National Institutes of Health grants from the National Institute on Aging (#R44AG055388 and #R43AG044863).
Publisher Copyright:
© 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Clinical trials need to specify which specific gait characteristics to monitor as mobility measures for each neurological disorder. As a first step, this study aimed to investigate a set of measures from daily-life monitoring that best discriminate mobility between people with multiple sclerosis (MS) and age-matched healthy control subjects (MS-Ctl) and between people with Parkinson’s disease (PD) and age-matched healthy control subjects (PD-Ctl). Further, we investigated how these discriminative measures relate to the disease severity of MS or PD. We recruited 13 people with MS, 21 MS-Ctl, 29 people with idiopathic PD, and 20 PD-Ctl. Subjects wore 3 inertial sensors on their feet and the lumbar back for a week. The Area Under Curves (AUC) from the receiver operator characteristic (ROC) plot was calculated for each measure to determine the objective measures that best separated the MS and PD groups from their respective control cohorts. Adherence wearing the sensors was similar among groups for 58–66 h of recording (p = 0.14). Quantity of mobility (activity measures, such as a median number of strides per gait bout, AUC = 0.93) best discriminated mobility impairments in MS from MS-Ctl. In contrast, quality of mobility (such as turn angle, AUC = 0.90) best discriminated mobility impairments in PD from PD-Ctl. Mobility measures with AUC > 0.80 were correlated with MS and PD clinical scores of disease severity. Thus, measures characterizing mobility impairments differ for MS versus PD during daily life suggesting that mobility measures for clinical trials and clinical practice need to be specific to each neurological disorder.
AB - Clinical trials need to specify which specific gait characteristics to monitor as mobility measures for each neurological disorder. As a first step, this study aimed to investigate a set of measures from daily-life monitoring that best discriminate mobility between people with multiple sclerosis (MS) and age-matched healthy control subjects (MS-Ctl) and between people with Parkinson’s disease (PD) and age-matched healthy control subjects (PD-Ctl). Further, we investigated how these discriminative measures relate to the disease severity of MS or PD. We recruited 13 people with MS, 21 MS-Ctl, 29 people with idiopathic PD, and 20 PD-Ctl. Subjects wore 3 inertial sensors on their feet and the lumbar back for a week. The Area Under Curves (AUC) from the receiver operator characteristic (ROC) plot was calculated for each measure to determine the objective measures that best separated the MS and PD groups from their respective control cohorts. Adherence wearing the sensors was similar among groups for 58–66 h of recording (p = 0.14). Quantity of mobility (activity measures, such as a median number of strides per gait bout, AUC = 0.93) best discriminated mobility impairments in MS from MS-Ctl. In contrast, quality of mobility (such as turn angle, AUC = 0.90) best discriminated mobility impairments in PD from PD-Ctl. Mobility measures with AUC > 0.80 were correlated with MS and PD clinical scores of disease severity. Thus, measures characterizing mobility impairments differ for MS versus PD during daily life suggesting that mobility measures for clinical trials and clinical practice need to be specific to each neurological disorder.
KW - Mobility
KW - Multiple sclerosis
KW - Neurological disorders
KW - Parkinson’s disease
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UR - http://www.scopus.com/inward/citedby.url?scp=85078610249&partnerID=8YFLogxK
U2 - 10.1007/s00415-020-09696-5
DO - 10.1007/s00415-020-09696-5
M3 - Article
C2 - 31927614
AN - SCOPUS:85078610249
SN - 0340-5354
VL - 267
SP - 1188
EP - 1196
JO - Journal of Neurology
JF - Journal of Neurology
IS - 4
ER -