% 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{Wisch:281816,
author = {Wisch, Julie K and McKay, Nicole S and Zammit, Matthew and
Christian, Bradley T and Schultz, Stephanie A and Millar,
Peter R and Ryan, Natalie S and Cash, David M and Belder,
Christopher R S and Chrem, Patricio and Cruchaga, Carlos and
Ibanez, Laura and Jucker, Mathias and Yakushev, Igor and
Day, Gregory S and Murphy, Mei and Llibre-Guerra, Jorge and
Aguillon, David and Roh, Jee Hoon and Xiong, Chengjie and
Wang, Guoqiao and Li, Yan and Schindler, Suzanne E and Jack,
Cliff and McDade, Eric and Bateman, Randall J and Benzinger,
Tammie L S and Ances, Beau M and Betthauser, Tobey and
Gordon, Brian},
collaboration = {Networ, Dominantly Inherited Alzheimer},
title = {{C}omparison of amyloid chronicity and {EYO} in autosomal
dominant {A}lzheimer's disease.},
journal = {Alzheimer's and dementia},
volume = {21},
number = {10},
issn = {1552-5260},
address = {Hoboken, NJ},
publisher = {Wiley},
reportid = {DZNE-2025-01198},
pages = {e70812},
year = {2025},
abstract = {Preclinical Alzheimer's disease (AD) can be described
relative to biomarker positivity onset time.We estimated
time from amyloid positivity (A+) using sampled iterative
local approximation (SILA) in a longitudinal autosomal
dominant AD (ADAD) sample (N = 379) with amyloid positron
emission tomography. We compared (1) predicted age at A+ to
imputed age, (2) estimated age at A+ to estimated age at
symptom onset, and (3) variance in cognitive performance
explained.Mean error between imputed and SILA-estimated age
at A+ (N = 26) was 1.15 years. Age at A+ explained $39\%$ of
estimated years to symptom onset (EYO) variance. Time from
A+ explained $19\%$ of cognitive composite variance and
$14\%$ of Clinical Dementia Rating Sum of Boxes CDR-SB
variance; EYO explained $43\%$ and $57\%,$ respectively.SILA
estimates A+ age in ADAD with reasonably good accuracy.
SILA-estimated time from A+ describes the start of
pathology, but the time from A+ onset to symptoms is
variable in ADAD and better described by EYO.Amyloid
chronicity predicts a 14-year preclinical AD phase in ADAD.
SILA accurately estimates age at A+ (MAE < 2 years). EYO
outperforms chronicity in predicting symptom onset. APP
mutation carriers show atypical amyloid accumulation.
Chronicity models help reveal AD heterogeneity in
preclinical stages.},
keywords = {Humans / Alzheimer Disease: genetics / Alzheimer Disease:
diagnostic imaging / Alzheimer Disease: pathology /
Alzheimer Disease: metabolism / Male / Female /
Positron-Emission Tomography / Middle Aged / Age of Onset /
Longitudinal Studies / Aged / Biomarkers / Disease
Progression / Amyloid: metabolism / Amyloid beta-Peptides:
metabolism / Alzheimer's disease (Other) / biomarkers
(Other) / genetic causes of Alzheimer's disease (Other) /
numeric methods (Other) / Biomarkers (NLM Chemicals) /
Amyloid (NLM Chemicals) / Amyloid beta-Peptides (NLM
Chemicals)},
cin = {AG Jucker},
ddc = {610},
cid = {I:(DE-2719)1210001},
pnm = {352 - Disease Mechanisms (POF4-352)},
pid = {G:(DE-HGF)POF4-352},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41137622},
doi = {10.1002/alz.70812},
url = {https://pub.dzne.de/record/281816},
}