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Memory impairment on free and cued selective reminding predicts dementia.
1Department of Neurology, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY 10461, USA. ehgrober@dti.net
Neurology
|February 26, 2000
Summary
Poor memory recall, specifically free recall from the Free and Cued Selective Reminding (FCSR) test, significantly predicts future dementia risk in older adults. This memory impairment may indicate a preclinical stage of dementia years before diagnosis.
Area of Science:
- Neurology
- Gerontology
- Cognitive Science
Background:
- Identifying individuals at high risk for dementia is crucial for early intervention.
- Memory impairment not attributable to other cognitive deficits can be identified using controlled memory tests.
- Inadequate control of testing conditions can lead to misidentification of dementia-related memory deficits.
Purpose of the Study:
- To determine the relative rates of dementia in individuals with and without memory impairment identified by baseline free recall using the Free and Cued Selective Reminding (FCSR) test.
Main Methods:
- Longitudinal study of 264 initially nondemented elderly volunteers from the Einstein Aging Study.
- Clinical and psychometric examinations conducted every 12 to 18 months for up to 10 years.
- Dementia diagnosis based on an algorithmic definition including Blessed Information Memory and Concentration score and evidence of functional decline.
Main Results:
- Thirty-two cases of incident dementia were observed during the follow-up period.
- Survival analyses revealed that subjects with impaired baseline free recall had significantly higher rates of dementia development (relative risk = 75.2) within 5 years compared to those with intact free recall.
- These findings remained significant after adjusting for age, gender, and education.
Conclusions:
- Impaired free recall performance on the FCSR test is a strong predictor of future dementia.
- The results support the existence of a preclinical phase of dementia characterized by memory impairment detectable at least 5 years prior to clinical diagnosis.