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Published on: July 31, 2019
Lateralized readiness potentials reveal motor slowing in the aging brain
Alexa B Roggeveen1, David J Prime, Lawrence M Ward
12136 West Mall, Department of Psychology, University of British Columbia, British Columbia, Canada. alexar@interchange.ubc.ca
Summary
Older adults exhibit slower reaction times (RTs) due to motor slowing, not perceptual deficits. The lateralized readiness potential (LRP) confirmed motor processes, not cognitive ones, cause age-related delays in motion detection.
Area of Science:
- Neuroscience
- Cognitive Aging
- Human Motor Control
Background:
- Older adults exhibit slower reaction times (RTs) compared to younger individuals, particularly in response to motion onset.
- The underlying causes of this age-related slowing are debated, with hypotheses including cognitive slowing and motor slowing.
Purpose of the Study:
- To investigate the specific origins of slowed reaction times to motion onset in older adults.
- To differentiate between perceptual/decision-making processes and motor programming/execution as causes of age-related slowing.
Main Methods:
- Utilized electroencephalogram (EEG) to measure the lateralized readiness potential (LRP).
- Participants identified the direction of motion (up/down) after its onset, with RTs recorded.
- LRP analysis was employed to distinguish between perceptual and motor contributions to RT differences.
Main Results:
- Older participants demonstrated significantly slower RTs compared to younger participants.
- LRP data indicated that the majority of the slowed response in older adults stemmed from motor processes.
- Perceptual processing did not appear to be the primary cause of the observed RT delays.
Conclusions:
- The slowed reaction times in older adults responding to motion onset are predominantly attributable to motor slowing.
- Findings suggest age-related changes in motor programming and execution contribute more significantly than perceptual deficits.
- The study provides insights into motion processing and neural inhibition in the aging brain.

