Dissociable effects of <i>APOE</i>-ε4 and β-amyloid pathology on visual working memory.

Abstract

Although <i>APOE</i>-ε4 carriers are at significantly higher risk of developing Alzheimer's disease than non-carriers¹, controversial evidence suggests that <i>APOE</i>-ε4 might confer some advantages, explaining the survival of this gene (antagonistic pleiotropy)^2,3. In a population-based cohort born in one week in 1946 (assessed aged 69-71), we assessed differential effects of <i>APOE</i>-ε4 and β-amyloid pathology (quantified using ¹⁸F-Florbetapir-PET) on visual working memory (object-location binding). In 398 cognitively normal participants, <i>APOE</i>-ε4 and β-amyloid had opposing effects on object identification, predicting better and poorer recall respectively. ε4-carriers also recalled locations more precisely, with a greater advantage at higher β-amyloid burden. These results provide evidence of superior visual working memory in ε4-carriers, showing that some benefits of this genotype are demonstrable in older age, even in the preclinical stages of Alzheimer's disease.