Aerobic exercise for Alzheimer's disease: A randomized controlled pilot trial
Jill K Morris1, Eric D Vidoni1, David K Johnson2
1University of Kansas Alzheimer's Disease Center, Fairway, KS, United States of America.
Aerobic exercise in early Alzheimer's disease (AD) improved functional ability. Gains in cardiorespiratory fitness correlated with better memory and reduced hippocampal atrophy, suggesting fitness is key for brain benefits.
Area of Science:
- Neurology
- Gerontology
- Exercise Science
Background:
- Alzheimer's disease (AD) poses a growing challenge, increasing interest in non-pharmacological interventions like physical exercise.
- Early intervention is crucial for managing AD progression and maintaining cognitive and functional abilities.
Purpose of the Study:
- To evaluate the impact of a 26-week supervised aerobic exercise program on memory, executive function, functional ability, and depression in individuals with early Alzheimer's disease (AD).
Main Methods:
- A 26-week randomized controlled trial involving 76 participants with early AD, comparing aerobic exercise (150 min/week) against a stretching and toning control group.
- Assessments included neuropsychological tests, functional ability surveys (Disability Assessment for Dementia), and depressive symptom scales (Cornell Scale for Depression in Dementia) at baseline, 13, and 26 weeks.
- Cardiorespiratory fitness and brain MRI were conducted at baseline and 26 weeks.
Main Results:
- Aerobic exercise demonstrated a modest but significant improvement in functional ability compared to the control group (p=0.02).
- No significant effects were observed on primary outcomes for memory, executive function, or depressive symptoms.
- Secondary analysis revealed a positive correlation between improved cardiorespiratory fitness and enhanced memory performance and hippocampal volume.
Conclusions:
- Supervised aerobic exercise offers benefits for functional ability in early Alzheimer's disease (AD).
- Improvements in cardiorespiratory fitness appear to be a key mechanism driving cognitive and brain structural benefits, including memory enhancement and reduced hippocampal atrophy.
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