Impaired H-Reflex Gain during Postural Loaded Locomotion in Individuals Post-Stroke

PLoS One. 2015 Dec 2;10(12):e0144007. doi: 10.1371/journal.pone.0144007. eCollection 2015.

Abstract

Objective: Successful execution of upright locomotion requires coordinated interaction between controllers for locomotion and posture. Our earlier research supported this model in the non-impaired and found impaired interaction in the post-stroke nervous system during locomotion. In this study, we sought to examine the role of the Ia afferent spinal loop, via the H-reflex response, under postural influence during a locomotor task. We tested the hypothesis that the ability to increase stretch reflex gain in response to postural loads during locomotion would be reduced post-stroke.

Methods: Fifteen individuals with chronic post-stroke hemiparesis and 13 non-impaired controls pedaled on a motorized cycle ergometer with specialized backboard support system under (1) seated supported, and (2) non-seated postural-loaded conditions, generating matched pedal force outputs of two levels. H-reflexes were elicited at 90° crank angle.

Results: We observed increased H-reflex gain with postural influence in non-impaired individuals, but a lack of increase in individuals post-stroke. Furthermore, we observed decreased H-reflex gain at higher postural loads in the stroke-impaired group.

Conclusion: These findings suggest an impaired Ia afferent pathway potentially underlies the defects in the interaction between postural and locomotor control post-stroke and may explain reduced ability of paretic limb support during locomotor weight-bearing in individuals post-stroke.

Significance: These results support the judicious use of bodyweight support training when first helping individuals post-stroke to regain locomotor pattern generation and weight-bearing capability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electromyography
  • Humans
  • Locomotion*
  • Middle Aged
  • Postural Balance*
  • Stroke / physiopathology*

Associated data

  • figshare/10.6084/M9.FIGSHARE.1604869

Grants and funding

This work was supported by the American Heart Association #11PRE54300029. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.