% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Soch:155514,
author = {Soch, Joram and Richter, Anni and Schütze, Hartmut and
Kizilirmak, Jasmin and Assmann, Anne and Behnisch, Gusalija
and Feldhoff, Hannah and Fischer, Larissa and Heil, Julius
and Knopf, Lea and Merkel, Christian and Raschick, Matthias
and Schietke, Clara-Johanna and Schult, Annika and
Seidenbecher, Constanze I and Yakupov, Renat and Ziegler,
Gabriel and Wiltfang, Jens and Düzel, Emrah and Schott,
Björn},
title = {{A} comprehensive score reflecting memory-related f{MRI}
activations and deactivations as potential biomarker for
neurocognitive aging.},
journal = {Human brain mapping},
volume = {42},
number = {14},
issn = {1097-0193},
address = {New York, NY},
publisher = {Wiley-Liss},
reportid = {DZNE-2021-00710},
pages = {4478-4496},
year = {2021},
abstract = {Older adults and particularly those at risk for developing
dementia typically show a decline in episodic memory
performance, which has been associated with altered memory
network activity detectable via functional magnetic
resonance imaging (fMRI). To quantify the degree of these
alterations, a score has been developed as a putative
imaging biomarker for successful aging in memory for older
adults (Functional Activity Deviations during Encoding,
FADE; Düzel et al., Hippocampus, 2011; 21: 803-814). Here,
we introduce and validate a more comprehensive version of
the FADE score, termed FADE-SAME (Similarity of Activations
during Memory Encoding), which differs from the original
FADE score by considering not only activations but also
deactivations in fMRI contrasts of stimulus novelty and
successful encoding, and by taking into account the variance
of young adults' activations. We computed both scores for
novelty and subsequent memory contrasts in a cohort of 217
healthy adults, including 106 young and 111 older
participants, as well as a replication cohort of 117 young
subjects. We further tested the stability and
generalizability of both scores by controlling for different
MR scanners and gender, as well as by using different data
sets of young adults as reference samples. Both scores
showed robust age-group-related differences for the
subsequent memory contrast, and the FADE-SAME score
additionally exhibited age-group-related differences for the
novelty contrast. Furthermore, both scores correlate with
behavioral measures of cognitive aging, namely memory
performance. Taken together, our results suggest that
single-value scores of memory-related fMRI responses may
constitute promising biomarkers for quantifying
neurocognitive aging.},
keywords = {Adolescent / Adult / Age Factors / Aged / Aged, 80 and over
/ Brain: diagnostic imaging / Brain: physiology / Cognitive
Aging: physiology / Female / Functional Neuroimaging:
methods / Hippocampus: diagnostic imaging / Hippocampus:
physiology / Humans / Magnetic Resonance Imaging / Male /
Memory, Episodic / Middle Aged / Young Adult / cognitive
aging (Other) / episodic memory (Other) / fMRI (Other) /
hippocampus (Other) / memory impairment (Other) / subsequent
memory effect (Other)},
cin = {AG Düzel / AG Wiltfang},
ddc = {610},
cid = {I:(DE-2719)5000006 / I:(DE-2719)1410006},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pmc = {pmc:PMC8410542},
pubmed = {pmid:34132437},
doi = {10.1002/hbm.25559},
url = {https://pub.dzne.de/record/155514},
}