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Responses to executive demand in young adulthood differ by APOE genotype
Rebecca Á Atkinson1, Darya Gaysina1, Jennifer M Rusted1
1School of Psychology, University of Sussex, Brighton, East Sussex, England, BN1 9QG, United Kingdom.
The Apolipoprotein E (APOE) ε4+ allele may offer cognitive advantages in young adults, particularly on complex tasks. These benefits appear linked to working memory and resource allocation, suggesting nuanced effects on cognitive aging.
Area of Science:
- Neuroscience
- Cognitive Psychology
- Genetics
Background:
- The Apolipoprotein E (APOE) ε4 allele is linked to cognitive decline but its early-life effects are unclear.
- Previous research on APOE ε4+ cognitive advantages in youth is inconsistent.
- Understanding lifespan cognitive effects of APOE ε4 is crucial for predicting cognitive aging.
Purpose of the Study:
- To investigate if APOE ε4+ confers cognitive advantages in young adults.
- To determine if these advantages are specific to executive functions under varying task demands.
- To explore the nature of cognitive performance differences between ε4+ and ε33 carriers.
Main Methods:
- Recruited young adults aged 18-25 years (21 ε4+, 63 ε33).
- Administered tasks measuring executive functions: verbal fluency, decision-making, prospective memory, and sustained attention.
- Systematically manipulated executive demand within tasks and measured subjective effort.
Main Results:
- Under low executive demand, ε4+ carriers made fewer verbal fluency word repeats.
- Under high executive demand, ε4+ carriers exhibited lower dual-task costs but more switching and root repetition errors.
- ε4+ carriers showed potential working memory updating advantages and different strategic approaches, including speed-accuracy trade-offs.
Conclusions:
- APOE ε4+ may provide cognitive benefits in young adulthood, especially under specific executive demands.
- Performance differences suggest ε4+ influences working memory updating and resource allocation strategies.
- These findings highlight the complex, context-dependent role of APOE ε4 in cognitive aging trajectories.
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