Abstract

Serial position performance was measured with the Buschke selective reminding test (BSRT). Hippocampal size was automatically measured via MRI using high-dimensional spatial transformation and a predefined hippocampus mask. We conducted regression analyses with delayed primacy, delayed recency and total delayed recall performance as outcome variables; predictors were age, family history of Alzheimer’s disease (AD), APOE e4 status, sex, level of education, total intracranial volume, and left and right hippocampal size. Results: The size of both the left and right hippocampus was positively correlated with delayed primacy performance, although left hippocampal size was a slightly better predictor of performance. In contrast, hippocampal size did not predict total delayed recall or recency performance. Conclusions:These findings are consistent with the hypothesis that the hippocampus is involved in delayed primacy consolidation. To our knowledge, this is the first time this has been reported in cognitively-intact older individuals, using in-vivo imaging. Our results shed some light on the relationship between delayed primacy performance and generalised cognitive decline. Since delayed primacy consolidation relies on a healthy hippocampus, and the hippocampus is affected early in AD, it is possible that failure to consolidate delayed primacy items might indirectly signal the incipient emergence of the disease.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call