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@ARTICLE{Fischer:281854,
author = {Fischer, Larissa and Adams, Jenna N and Molloy, Eóin N.
and Tremblay-Mercier, Jennifer and Remz, Jordana and
Binette, Alexa Pichet and Rajah, M Natasha and Villeneuve,
Sylvia and Maass, Anne},
collaboration = {Group, PREVENT-AD Research},
othercontributors = {Poirier, Judes and Breitner, John C S and Badawy, Mohamed
and Baillet, Sylvain and Baril, Andrée-Ann and Bellec,
Pierre and Bohbot, Véronique and Bzdok, Danilo and
Chakravarty, Mallar and Collins, D Louis and Dadar, Mahsa
and Ducharme, Simon and Evans, Alan and Gauthier, Claudine
and Geddes, Maiya R and Hoge, Rick and Ituria-Medina, Yasser
and Multhaup, Gerhard and Münter, Lisa-Marie and Rajah, M
Natasha and Rosa-Neto, Pedro and Schmitz, Taylor and Soucy,
Jean-Paul and Spreng, Nathan and Tardif, Christine and
Vachon-Presseau, Etienne and Bocti, Christian and
Descoteaux, Maxime and Laforce, Robert and Binette, Alexa
Pichet},
title = {{L}ongitudinal functional connectivity during rest and task
is differentially related to {A}lzheimer's pathology and
episodic memory in older adults.},
journal = {Scientific reports},
volume = {15},
number = {1},
issn = {2045-2322},
address = {[London]},
publisher = {Springer Nature},
reportid = {DZNE-2025-01227},
pages = {38499},
year = {2025},
abstract = {Changes in functional connectivity (FC) strength involving
the medial temporal lobe (MTL) and posteromedial cortex
(PMC) are related to early Alzheimer's pathology and
alterations in episodic memory performance in cognitively
unimpaired older adults, but their dynamics remain unclear.
We examined how longitudinal changes in FC involving MTL and
PMC during resting-state, episodic memory encoding, and
retrieval relate to subsequent amyloid- and tau-PET burden,
longitudinal episodic memory performance, and the APOE4
genotype in 152 cognitively unimpaired older adults from the
PREVENT-AD cohort. We found APOE4- and fMRI
paradigm-dependent associations of change in FC strength
with pathology burden and change in episodic memory
performance. Decreasing FC over time, or 'hypoconnectivity',
within PMC during rest in APOE4 carriers and during
retrieval in APOE4 non-carriers was related to more amyloid
and tau, respectively. Conversely, increasing FC over time,
or 'hyperconnectivity', within MTL during encoding in APOE4
carriers and between MTL and PMC during retrieval
independent of APOE4 status was related to more tau.
Further, increasing FC between MTL and PMC during rest,
unlike during encoding, was beneficial for episodic memory.
Our study highlights that pathology-related episodic memory
network changes manifest differently during rest and task
and have differential implications for episodic memory
trajectories.},
keywords = {Humans / Memory, Episodic / Alzheimer Disease:
physiopathology / Alzheimer Disease: pathology / Alzheimer
Disease: diagnostic imaging / Alzheimer Disease: metabolism
/ Aged / Female / Male / Magnetic Resonance Imaging /
Apolipoprotein E4: genetics / Rest: physiology / Temporal
Lobe: physiopathology / Temporal Lobe: diagnostic imaging /
Temporal Lobe: pathology / tau Proteins: metabolism /
Longitudinal Studies / Aged, 80 and over / Positron-Emission
Tomography / Middle Aged / APOE4 (Other) / Aging (Other) /
Alzheimer’s disease (Other) / Episodic memory (Other) /
Functional connectivity (Other) / fMRI (Other) /
Apolipoprotein E4 (NLM Chemicals) / tau Proteins (NLM
Chemicals)},
cin = {AG Maaß},
ddc = {600},
cid = {I:(DE-2719)1311001},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41188354},
doi = {10.1038/s41598-025-21596-0},
url = {https://pub.dzne.de/record/281854},
}