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@ARTICLE{Hobert:140489,
author = {Hobert, Markus A and Nussbaum, Susanne and Heger, Tanja and
Berg, Daniela and Maetzler, Walter and Heinzel, Sebastian},
title = {{P}rogressive {G}ait {D}eficits in {P}arkinson's {D}isease:
{A} {W}earable-{B}ased {B}iannual 5-{Y}ear {P}rospective
{S}tudy.},
journal = {Frontiers in aging neuroscience},
volume = {11},
issn = {1663-4365},
address = {Lausanne},
publisher = {Frontiers Research Foundation},
reportid = {DZNE-2020-06811},
pages = {22},
year = {2019},
abstract = {Background: Gait changes occur during all Parkinson’s
disease (PD) stages and wearable sensor-derived gait
parameters may quantify PD progression. However, key aspects
that may qualify quantitative gait parameters as progression
markers in PD remain elusive.Objectives: Longitudinal
changes in gait parameters from a lower-back sensor under
convenient and challenging walking conditions in early- and
mid-stage PD patients (E-PD, M-PD) compared to controls were
investigated.Methods: Normal- and fast-pace parameters
(step: number, time, velocity, variability) were assessed
every 6 months for up to 5 years in 22 E-PD (<4 years
baseline disease duration), 18 M-PD (>5 years) and 24
controls. Parameter trajectories and associations with
MDS-UPDRS-III were tested using generalized estimating
equations.Results: Normal-pace step number (annual change in
E-PD: $2.1\%,$ Time∗Group: p = 0.001) and step time
variability $(8.5\%,$ p < 0.05) longitudinally increased in
E-PD compared to controls $(0.7\%,$ $-12\%).$ For fast pace,
no significant progression differences between groups were
observed. Longitudinal changes in M-PD did not differ
significantly from controls. MDS-UPDRS-III was largely
associated with normal-pace parameters in M-PD.Conclusion:
Wearables can quantify progressive gait deficits indicated
by increasing step number and step time variability in E-PD.
In M-PD, and for fast-pace, gait parameters possess limited
potential as PD progression markers.},
cin = {Ext UKT / AG Gasser / Tübingen Pre 2020 / AG Berg / AG
Maetzler},
ddc = {610},
cid = {I:(DE-2719)5000058 / I:(DE-2719)1210000 /
I:(DE-2719)6000018 / I:(DE-2719)5000055 /
I:(DE-2719)5000024},
pnm = {344 - Clinical and Health Care Research (POF3-344) / 345 -
Population Studies and Genetics (POF3-345)},
pid = {G:(DE-HGF)POF3-344 / G:(DE-HGF)POF3-345},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:30814947},
pmc = {pmc:PMC6381067},
doi = {10.3389/fnagi.2019.00022},
url = {https://pub.dzne.de/record/140489},
}