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Association between Various Brain Pathologies and Gait Disturbance.
Alexandra M V Wennberg1, Rodolfo Savica, Michelle M Mielke
1Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Dementia and Geriatric Cognitive Disorders
|February 3, 2017
Summary
Neuropathology, including grey matter atrophy and protein aggregates like amyloid and tau, is linked to gait disruption in older adults. More longitudinal research is needed to understand these complex relationships.
Area of Science:
- Neurology
- Gerontology
- Biomedical Science
Background:
- Approximately 30% of older adults experience disrupted gait, a condition linked to increased risks of cognitive decline, disability, dementia, and mortality.
- Many older adults exhibit neuropathologies, prompting research into the connection between subclinical brain changes and gait disturbances.
- Investigating the link between neuropathology and gait is crucial for understanding age-related functional decline.
Purpose of the Study:
- To review and synthesize existing research on the association between various neuropathologies and gait parameters in older adults.
- To identify which neuropathologies are most consistently linked to gait impairment.
- To highlight gaps in current knowledge and suggest future research directions.
Main Methods:
- Systematic review of studies examining the relationship between gait and neuropathologies.
- Analysis of findings related to grey matter atrophy, white matter changes, neuronal activity, and protein aggregation (amyloid, tau).
- Assessment of methodological approaches and study designs, including a focus on longitudinal data.
Main Results:
- Grey matter atrophy showed the most consistent association with poorer gait performance across reviewed studies.
- White matter studies primarily focused on total white matter, suggesting a need for regional analysis.
- Evidence indicates both under- and overactivation in neuronal activity are linked to gait disruption, requiring further clarification.
- Early findings suggest amyloid and tau aggregation negatively impact gait, but more research is needed.
Conclusions:
- Subclinical neuropathologies, particularly grey matter atrophy, are associated with gait disruption in older adults.
- Conflicting results regarding neuronal activity and gait necessitate further investigation.
- Substantial methodological heterogeneity and a lack of longitudinal studies limit current understanding.
- Longitudinal research tracking neuropathology and gait changes is essential for understanding disease trajectories.
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