Rate control deficits during pinch grip and ankle dorsiflexion in early-stage Parkinson's disease

PLoS One. 2023 Mar 3;18(3):e0282203. doi: 10.1371/journal.pone.0282203. eCollection 2023.

Abstract

Background: Much of our understanding of the deficits in force control in Parkinson's disease (PD) relies on findings in the upper extremity. Currently, there is a paucity of data pertaining to the effect of PD on lower limb force control.

Objective: The purpose of this study was to concurrently evaluate upper- and lower-limb force control in early-stage PD and a group of age- and gender-matched healthy controls.

Methods: Twenty individuals with PD and twenty-one healthy older adults participated in this study. Participants performed two visually guided, submaximal (15% of maximum voluntary contractions) isometric force tasks: a pinch grip task and an ankle dorsiflexion task. PD were tested on their more affected side and after overnight withdrawal from antiparkinsonian medication. The tested side in controls was randomized. Differences in force control capacity were assessed by manipulating speed-based and variability-based task parameters.

Results: Compared with controls, PD demonstrated slower rates of force development and force relaxation during the foot task, and a slower rate of relaxation during the hand task. Force variability was similar across groups but greater in the foot than in the hand in both PD and controls. Lower limb rate control deficits were greater in PD with more severe symptoms based on the Hoehn and Yahr stage.

Conclusions: Together, these results provide quantitative evidence of an impaired capacity in PD to produce submaximal and rapid force across multiple effectors. Moreover, results suggest that force control deficits in the lower limb may become more severe with disease progression.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Ankle*
  • Case-Control Studies
  • Foot
  • Hand
  • Hand Strength*
  • Humans
  • Lower Extremity
  • Parkinson Disease* / physiopathology