# Sex and APOE ε2 Interactive Effects on the Longitudinal Change in Cognition in a Population-Based Cohort of Older Adults with Vascular Risk Factors

**Authors:** Noemí Lamonja-Vicente, Rosalía Dacosta-Aguayo, Jorge López-Olóriz, Laia Prades-Senovilla, Juan José Soriano-Raya, Inmaculada C. Clemente, Júlia Miralbell, Maite Barrios, Elena López-Cancio, Cynthia Cáceres, Mónica Millán, Pere Torán, Guillem Pera, Meritxell Carmona-Cervelló, Cecilia Herrero, Pilar Montero-Alia, Maria Palau-Antoja, Maria Hernández-Pérez, Tamara Canento, Ana Gonzalez Fuxa, Maria Mataró, Marc Via

PMC · DOI: 10.3390/ijms262110591 · International Journal of Molecular Sciences · 2025-10-30

## TL;DR

This study explores how the APOE ε2 gene variant interacts with sex to affect cognitive decline in older adults with vascular risk factors.

## Contribution

The study reveals that APOE ε2 may have a detrimental effect on verbal memory in aging males, challenging its assumed protective role.

## Key findings

- APOE ε2 does not consistently protect cognition over time.
- Regression to the mean effects were significant, especially in ε2 carriers.
- Aging males with APOE ε2 showed worse verbal memory decline.

## Abstract

Cognitive aging trajectories differ widely across individuals, and genetic factors such as APOE and BDNF polymorphisms may contribute to this variability. While APOE ε4 has been widely studied, the influence of APOE ε2, particularly in interaction with sex, remains underexplored. This study aims to examine the longitudinal trajectory of APOE ε2 individuals on cognitive performance, and their interactions with sex, age, and BDNF Val66Met polymorphism, in a population-based cohort of older adults with vascular risk. We analyzed data from 386 participants (mean age: 71.8) from the Barcelona-AsIA Neuropsychology Study, followed over a 7-year period. Verbal memory, verbal fluency, and visuospatial domains were assessed. Linear regression models tested associations between cognitive change and genotypes, controlling for age, sex, education, depression, and vascular risk. Interaction terms and permutation testing were applied. Regression to the mean (RTM) effects were assessed. BDNF showed no significant associations with cognitive performance. RTM effects were evident across subgroups, particularly among ε2 carriers, suggesting this phenomenon partly explains the divergent results over time. APOE ε2 does not confer a consistent protective effect on cognition over time. Our results highlight that APOE ε2 may be detrimental to verbal memory in aging males.

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348], BDNF (brain derived neurotrophic factor) [NCBI Gene 627]

## Full-text entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}
- **Diseases:** depression (MESH:D003866)
- **Mutations:** Val66Met

## Full text

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## Figures

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## References

100 references — full list in the complete paper: https://tomesphere.com/paper/PMC12607810/full.md

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Source: https://tomesphere.com/paper/PMC12607810