Precuneus Activity during Retrieval Is Positively Associated with Amyloid Burden in Cognitively Normal Older <i>APOE</i> 4 Carriers

L Larissa Fischer E Eóin N. Molloy A Alexa Pichet Binette N Niklas Vockert J Jonas Marquardt A Andrea Pacha Pilar M Michael C. Kreissl J Jordana Remz J Jennifer Tremblay-Mercier (Douglas Mental Health University Institute) J Judes Poirier (Douglas Mental Health University Institute) M Maria Natasha Rajah S Sylvia Villeneuve (Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University) A Anne Maass

Abstract

The precuneus is a site of early amyloid-beta (Aβ) accumulation. Previous cross-sectional studies reported increased precuneus fMRI activity in older adults with mild cognitive deficits or elevated Aβ. However, longitudinal studies in early Alzheimer's disease (AD) are lacking and the relationship to the Apolipoprotein-E ( APOE ) genotype is unclear. Investigating the PREVENT-AD dataset, we assessed how baseline and longitudinal precuneus activity during successful memory retrieval relates to future Aβ and tau burden and change in memory performance. We further studied the moderation by APOE 4 genotype. We included 165 older adults (age, 62.8 ± 4.4 years; 113 female; 66 APOE 4 carriers) who were cognitively normal at baseline with a family history of AD. All participants performed task-fMRI at baseline and underwent 18 F-flortaucipir-PET and 18 F-NAV4694-Aβ-PET on average 5 years later. We found that higher baseline activity and greater longitudinal increase in precuneus activity were associated with higher Aβ burden in APOE 4 carriers but not noncarriers. We observed no effects of precuneus activity on tau burden. Finally, APOE 4 noncarriers with low baseline precuneus activity exhibited better longitudinal performance in an independent memory test compared with (1) noncarriers with higher baseline activity and (2) APOE 4 carriers. Our findings suggest that higher task-related precuneus activity during memory retrieval at baseline and over time are associated with greater Aβ burden in cognitively normal APOE 4 carriers. Our results further indicate that the absence of “hyperactivation” and the absence of the APOE 4 allele is related with better future cognitive outcomes in cognitively normal older adults at risk for AD.

Article Details

Volume / Issue Vol. 45, Issue 6
Published February 05, 2025
Pages e1408242024
ISSN 0270-6474
Publisher Society for Neuroscience

Journal Info

Journal of Neuroscience

Society for Neuroscience

ISSN: 0270-6474 Life Sciences

Authors (13)

L

Larissa Fischer

E

Eóin N. Molloy

A

Alexa Pichet Binette

N

Niklas Vockert

J

Jonas Marquardt

A

Andrea Pacha Pilar

M

Michael C. Kreissl

J

Jordana Remz

J

Jennifer Tremblay-Mercier

Douglas Mental Health University Institute

J

Judes Poirier

Douglas Mental Health University Institute

M

Maria Natasha Rajah

S

Sylvia Villeneuve

Montreal Neurological Institute, Department of Neurology and Neurosurgery, McGill University

A

Anne Maass