TY - JOUR
T1 - Prism adaptation in Parkinson disease
T2 - comparing reaching to walking and freezers to non-freezers
AU - Nemanich, Samuel T.
AU - Earhart, Gammon M.
N1 - Funding Information:
The authors thank Ryan Duncan, Martha Hessler, and Richard Nagel for assistance with data collection and evaluation of PD participants and Kendra Cherry, Ryan Duncan, and Marie McNeely for helpful manuscript feedback. This work was supported by grants from the Parkinson’s and Movement Disorder Foundation, The Program in Physical Therapy at Washington University, the National Institutes of Health R01 NS077959, and the Washington University Institute of Clinical and Translational Sciences Grants UL1 TR000448 and TL1 TR000449 from the National Center for Advancing Translational Sciences.
Publisher Copyright:
© 2015, Springer-Verlag Berlin Heidelberg.
PY - 2015/8/25
Y1 - 2015/8/25
N2 - Visuomotor adaptation to gaze-shifting prism glasses requires recalibration of the relationship between sensory input and motor output. Healthy individuals flexibly adapt movement patterns to many external perturbations; however, individuals with cerebellar damage do not adapt movements to the same extent. People with Parkinson disease (PD) adapt normally, but exhibit reduced after-effects, which are negative movement errors following the removal of the prism glasses and are indicative of true spatial realignment. Walking is particularly affected in PD, and many individuals experience freezing of gait (FOG), an episodic interruption in walking, that is thought to have a distinct pathophysiology. Here, we examined how individuals with PD with (PD + FOG) and without (PD − FOG) FOG, along with healthy older adults, adapted both reaching and walking patterns to prism glasses. Participants completed a visually guided reaching and walking task with and without rightward-shifting prism glasses. All groups adapted at similar rates during reaching and during walking. However, overall walking adaptation rates were slower compared to reaching rates. The PD − FOG group showed smaller after-effects, particularly during walking, compared to PD + FOG, independent of adaptation magnitude. While FOG did not appear to affect characteristics of prism adaptation, these results support the idea that the distinct neural processes governing visuomotor adaptation and storage are differentially affected by basal ganglia dysfunction in PD.
AB - Visuomotor adaptation to gaze-shifting prism glasses requires recalibration of the relationship between sensory input and motor output. Healthy individuals flexibly adapt movement patterns to many external perturbations; however, individuals with cerebellar damage do not adapt movements to the same extent. People with Parkinson disease (PD) adapt normally, but exhibit reduced after-effects, which are negative movement errors following the removal of the prism glasses and are indicative of true spatial realignment. Walking is particularly affected in PD, and many individuals experience freezing of gait (FOG), an episodic interruption in walking, that is thought to have a distinct pathophysiology. Here, we examined how individuals with PD with (PD + FOG) and without (PD − FOG) FOG, along with healthy older adults, adapted both reaching and walking patterns to prism glasses. Participants completed a visually guided reaching and walking task with and without rightward-shifting prism glasses. All groups adapted at similar rates during reaching and during walking. However, overall walking adaptation rates were slower compared to reaching rates. The PD − FOG group showed smaller after-effects, particularly during walking, compared to PD + FOG, independent of adaptation magnitude. While FOG did not appear to affect characteristics of prism adaptation, these results support the idea that the distinct neural processes governing visuomotor adaptation and storage are differentially affected by basal ganglia dysfunction in PD.
KW - After-effects
KW - Freezing of gait
KW - Parkinson disease
KW - Prism adaptation
UR - http://www.scopus.com/inward/record.url?scp=84937969888&partnerID=8YFLogxK
U2 - 10.1007/s00221-015-4299-4
DO - 10.1007/s00221-015-4299-4
M3 - Article
C2 - 25976516
AN - SCOPUS:84937969888
SN - 0014-4819
VL - 233
SP - 2301
EP - 2310
JO - Experimental Brain Research
JF - Experimental Brain Research
IS - 8
ER -