Apolipoprotein E polymorphism carriers exhibit objective cognitive deficits: a single center trial.
Yanfang Zeng1, Xin Huang1, Kenneth Elkin2
1Department of Neurology, Beijing Luhe Hospital, Capital Medical University , Beijing, China.
Apolipoprotein E (ApoE) ε4 carriers showed significantly poorer cognitive function, including memory, compared to non-carriers. This study highlights the association between ApoE genotype and cognitive performance in older adults.
Area of Science:
- Neuroscience
- Genetics
- Gerontology
Background:
- Apolipoprotein E (ApoE) polymorphism is a known genetic factor influencing cognitive function.
- Understanding the regional prevalence and impact of ApoE genotypes is crucial for cognitive health research.
Purpose of the Study:
- To investigate the correlation between objectively measured cognitive function and apolipoprotein E (ApoE) polymorphism in a specific geographic region.
- To analyze the distribution of ApoE genotypes and their association with cognitive performance in an elderly cohort.
Main Methods:
- Sixty-one patients aged 55-90 were enrolled from a memory clinic.
- Cognitive function was assessed using neuropsychological scales, including Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA).
- Apolipoprotein E (ApoE) genotyping was performed on venous blood samples using PCR amplification and chip hybridization.
Main Results:
- The most prevalent genotype was ε3/3 (40 patients), followed by ε3/4 (12 patients) and ε2/3 (7 patients).
- Allele frequencies were ε3 (81.15%), ε4 (13.11%), and ε2 (5.74%).
- Apolipoprotein E (ApoE) ε4 carriers exhibited significantly lower MMSE (18.14 ± 0.39) and MoCA (14.36 ± 7.56) scores compared to non-ε4 carriers (P < 0.05).
Conclusions:
- The ε3/3 genotype was the most common, with ε4 carriers demonstrating notable deficits in memory and overall cognitive function.
- The findings underscore the significant impact of apolipoprotein E (ApoE) ε4 carriage on cognitive performance in the studied population.
- This research contributes to understanding the genetic underpinnings of cognitive aging within a specific geographic context.
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