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A High Throughput, Multiplexed and Targeted Proteomic CSF Assay to Quantify Neurodegenerative Biomarkers and Apolipoprotein E Isoforms Status
Published on: October 20, 2016
Apolipoprotein E, cognitive function, and dementia in a general population aged 85 years and over
K Juva1, A Verkkoniemi, P Viramo
1Department of Clinical Neurosciences, Helsinki University Central Hospital, University of Helsinki, Finland. katijuva@katto.kaapeli.fi
The Apo-E epsilon4 gene variant increases dementia risk in the elderly, particularly in women. However, it does not appear to impair cognitive function in non-demented individuals who reach advanced age.
Area of Science:
- Gerontology
- Neuroscience
- Genetics
Background:
- Dementia is a growing public health concern in aging populations.
- The apolipoprotein E (Apo-E) epsilon4 allele is a known genetic risk factor for late-onset Alzheimer's disease.
- Understanding genetic influences on cognitive aging is crucial for developing targeted interventions.
Purpose of the Study:
- To investigate the prevalence of dementia in a Finnish elderly population.
- To determine the association between the Apo-E genotype and dementia risk.
- To explore the impact of the Apo-E epsilon4 allele on cognitive function in non-demented elderly individuals.
Main Methods:
- A population-based study of 510 individuals aged 85+ in a Finnish city.
- Assessment of cognitive function using the Mini-Mental State Examination (MMSE).
- Diagnosis of dementia according to DSM-III-R criteria and determination of Apo-E genotype.
Main Results:
- The prevalence of dementia was 38.6% in the study population.
- Apo-E epsilon4 carriers had a significantly higher odds ratio (OR) for dementia (2.36), especially women (OR 3.23).
- Mean MMSE scores differed between carriers and non-carriers in the overall population, but not within demented or non-demented subgroups.
Conclusions:
- The Apo-E epsilon4 allele is associated with an increased risk of dementia in the very old, with a pronounced effect in women.
- This study does not support the hypothesis that the Apo-E epsilon4 allele negatively impacts cognitive function in non-demented elderly individuals surviving to advanced age.
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