Title

Independent Contribution of Temporal β-amyloid Deposition to Memory Decline in the Pre-dementia Phase of Alzheimer's Disease

Document Type

Journal Article

Publisher

Oxford

Faculty

Faculty of Computing, Health and Science

School

School of Medical Sciences / Centre of Excellence for Alzheimer's Disease Research and Care

RAS ID

12598

Comments

This article was originally published as: Chetelat, G., Villemagne, V., Pike, K., Ellis, K., Bourgeat, P., Jones, G., O'Keefe, G., Salvado, O., Szoeke, C., Martins, R. N., Ames, D., Masters, C., & Rowe, C. (2011). Independent contribution of temporal β-amyloid deposition to memory decline in the pre-dementia phase of Alzheimer's disease. Brain, 134(3), 798-807. Original article available here

Abstract

The relationship between beta-amyloid deposition and memory deficits in early Alzheimer's disease is unresolved, as past studies show conflicting findings. The present study aims to determine the relative contribution of regional beta-amyloid deposition, hippocampal atrophy and white matter integrity to episodic memory deficits in non-demented older individuals harbouring one of the characteristic hallmarks of Alzheimer's disease, i.e. with beta-amyloid pathology. Understanding these relationships is critical for effective therapeutic development. Brain magnetic resonance imaging and [(11)C]Pittsburgh Compound B-positron emission tomography scans were obtained in 136 non-demented individuals aged over 60 years, including 93 healthy elderly and 43 patients with mild cognitive impairment. Voxel-based correlations were computed between a memory composite score and grey matter volume, white matter volume and beta-amyloid deposition imaging datasets. Hierarchical linear regression analyses were then performed using values extracted in regions of most significant correlations to determine the relative contribution of each modality to memory deficits. All analyses were conducted pooling all groups together as well as within separate subgroups of cognitively normal elderly, patients with mild cognitive impairment and individuals with high versus low neocortical beta-amyloid. Brain areas of highest correlation with episodic memory deficits were the hippocampi for grey matter volume, the perforant path for white matter volume and the temporal neocortex for beta-amyloid deposition. When considering these three variables together, only hippocampal volume and temporal beta-amyloid deposition provided independent contributions to memory deficits. In contrast to global beta-amyloid deposition, temporal beta-amyloid deposition was still related to memory independently from hippocampal atrophy within subgroups of cognitively normal elderly, patients with mild cognitive impairment or cases with high neocortical beta-amyloid. In the pre-dementia stage of Alzheimer's disease, subtle episodic memory impairment is related to beta-amyloid deposition, especially in the temporal neocortex, and independently from hippocampal atrophy, suggesting that both factors should be independently targeted in therapeutic trials aimed at reducing cognitive decline.

Access Rights

Open Access