Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.

<h4>Background</h4>GBA mutation carriers with PD (PD-GBA) are at higher risk of cognitive decline, but there is limited data regarding whether there are differences in gait dysfunction between GBA mutation and non-mutation carriers with PD.<h4>Objectives/methods</h4>The prima...

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Main Authors: Anjali Gera, Joan A O'Keefe, Bichun Ouyang, Yuanqing Liu, Samantha Ruehl, Mark Buder, Jessica Joyce, Nicolette Purcell, Gian Pal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0226494
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spelling doaj-7764a8dd5b9a4be2867c844048cbb4f82021-03-04T11:19:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-01151e022649410.1371/journal.pone.0226494Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.Anjali GeraJoan A O'KeefeBichun OuyangYuanqing LiuSamantha RuehlMark BuderJessica JoyceNicolette PurcellGian Pal<h4>Background</h4>GBA mutation carriers with PD (PD-GBA) are at higher risk of cognitive decline, but there is limited data regarding whether there are differences in gait dysfunction between GBA mutation and non-mutation carriers with PD.<h4>Objectives/methods</h4>The primary aim of this study was to use quantitative inertial sensor-based gait analysis to compare gait asymmetry in 17 PD-GBA subjects, 17 non-mutation carriers with PD, and 15 healthy control subjects using parameters that had gait laterality and were markers of bradykinesia, in particular arm swing velocity and arm swing range of motion and stride length.<h4>Results</h4>Arm swing velocity was more symmetric in PD-GBA subjects vs. non-mutation carriers in the OFF state (12.5 +/- 8.3 vs. 22.9 +/- 11.8%, respectively, p = 0.018). In the ON-medication state, non-mutation carriers with PD, but not PD-GBA subjects, exhibited arm swing velocity (16.8 +/- 8.6 vs. 22.9 +/- 11.8%, p = 0.006) and arm range of motion (26.7 +/- 16.3 vs. 33.4 +/- 18.6%, p = 0.02) that was more asymmetric compared with the OFF-medication state.<h4>Conclusions</h4>In the OFF medication state, arm swing velocity asymmetry may be a useful parameter in helping to distinguish GBA mutation carriers with PD from non-mutation carriers.https://doi.org/10.1371/journal.pone.0226494
collection DOAJ
language English
format Article
sources DOAJ
author Anjali Gera
Joan A O'Keefe
Bichun Ouyang
Yuanqing Liu
Samantha Ruehl
Mark Buder
Jessica Joyce
Nicolette Purcell
Gian Pal
spellingShingle Anjali Gera
Joan A O'Keefe
Bichun Ouyang
Yuanqing Liu
Samantha Ruehl
Mark Buder
Jessica Joyce
Nicolette Purcell
Gian Pal
Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
PLoS ONE
author_facet Anjali Gera
Joan A O'Keefe
Bichun Ouyang
Yuanqing Liu
Samantha Ruehl
Mark Buder
Jessica Joyce
Nicolette Purcell
Gian Pal
author_sort Anjali Gera
title Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
title_short Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
title_full Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
title_fullStr Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
title_full_unstemmed Gait asymmetry in glucocerebrosidase mutation carriers with Parkinson's disease.
title_sort gait asymmetry in glucocerebrosidase mutation carriers with parkinson's disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2020-01-01
description <h4>Background</h4>GBA mutation carriers with PD (PD-GBA) are at higher risk of cognitive decline, but there is limited data regarding whether there are differences in gait dysfunction between GBA mutation and non-mutation carriers with PD.<h4>Objectives/methods</h4>The primary aim of this study was to use quantitative inertial sensor-based gait analysis to compare gait asymmetry in 17 PD-GBA subjects, 17 non-mutation carriers with PD, and 15 healthy control subjects using parameters that had gait laterality and were markers of bradykinesia, in particular arm swing velocity and arm swing range of motion and stride length.<h4>Results</h4>Arm swing velocity was more symmetric in PD-GBA subjects vs. non-mutation carriers in the OFF state (12.5 +/- 8.3 vs. 22.9 +/- 11.8%, respectively, p = 0.018). In the ON-medication state, non-mutation carriers with PD, but not PD-GBA subjects, exhibited arm swing velocity (16.8 +/- 8.6 vs. 22.9 +/- 11.8%, p = 0.006) and arm range of motion (26.7 +/- 16.3 vs. 33.4 +/- 18.6%, p = 0.02) that was more asymmetric compared with the OFF-medication state.<h4>Conclusions</h4>In the OFF medication state, arm swing velocity asymmetry may be a useful parameter in helping to distinguish GBA mutation carriers with PD from non-mutation carriers.
url https://doi.org/10.1371/journal.pone.0226494
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