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Aβ-related memory decline in APOE ε4 noncarriers
Journal article   Peer reviewed

Aβ-related memory decline in APOE ε4 noncarriers

Y.Y. Lim, S.M. Laws, V.L. Villemagne, R.H. Pietrzak, T. Porter, D. Ames, C. Fowler, S. Rainey-Smith, P.J. Snyder, R.N. Martins, …
Neurology, Vol.86(17), pp.1635-1642
2016
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Abstract

Objective: As the absence of Aβ-related memory decline in APOE ε4 noncarriers may be due to the relative brevity of previous studies, we aimed to characterize Aβ-related cognitive decline over 72 months in APOE ε4 carriers and noncarriers who were cognitively normal (CN). Methods: CN older adults (n = 423) underwent Aβ imaging and APOE genotyping. Participants completed comprehensive neuropsychological testing at baseline 18-, 36-, 54-, and 72-month assessments. Results: Relative to Aβ− CN ε4 noncarriers, both Aβ+ CN ε4 carriers and noncarriers showed significantly increased decline in measures of memory, language, and executive function as well as higher rates of progression to a clinical classification of mild cognitive impairment. Memory decline was greater in Aβ+ CN ε4 carriers than in Aβ+ CN ε4 noncarriers. No cognitive decline was evident in Aβ− CN ε4 carriers. Conclusions: In CN older adults, Aβ+ is associated with memory decline in ε4 noncarriers; however, the rate of this decline is much slower than that observed in ε4 carriers. These data indicate that the processes by which ε4 carriage increases the rate of Aβ-related cognitive decline occur in the preclinical stage of Alzheimer disease.

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Collaboration types
Industry collaboration
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International collaboration
Citation topics
1 Clinical & Life Sciences
1.52 Neurodegenerative Diseases
1.52.60 Dementia
Web Of Science research areas
Clinical Neurology
ESI research areas
Neuroscience & Behavior
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