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@ARTICLE{Oomens:282559,
author = {Oomens, Julie E and Vos, Stephanie Jb and Maserejian, Nancy
N and Boada, Mercè and Didic, Mira and Engelborghs,
Sebastiaan and Fladby, Tormod and van der Flier, Wiesje M
and Frisoni, Giovanni B and Fröhlich, Lutz and Gill, Kiran
Dip and Grimmer, Timo and Hort, Jakub and Itoh, Yoshiaki and
Iwatsubo, Takeshi and Klimkowicz-Mrowiec, Aleksandra and
Landau, Susan M and Lee, Dong Young and Lleó, Alberto and
Martinez-Lage, Pablo and de Mendonça, Alexandre and Meyer,
Philipp T and Parchi, Piero and Pardini, Matteo and
Parnetti, Lucilla and Popp, Julius and Rami, Lorena and
Reiman, Eric M and Rinne, Juha O and Rodrigue, Karen M and
Sánchez-Juan, Pascual and Santana, Isabel and Scarmeas,
Nikolaos and Scheltens, Philip and Skoog, Ingmar and
Sperling, Reisa A and Stern, Yaakov and Villeneuve, Sylvia
and Waldemar, Gunhild and Wiltfang, Jens and Zetterberg,
Henrik and Alcolea, Daniel and Allegri, Ricardo F and
Altomare, Daniele and Bateman, Randall J and Baiardi, Simone
and Baldeiras, Ines and Blennow, Kaj and Braber, Anouk den
and van Buchem, Mark A and Byun, Min Soo and Cerman, Jiří
and Chen, Kewei and Chipi, Elena and Day, Gregory S and
Drzezga, Alexander and Ekblad, Laura L and Förster, Stefan
and Fortea, Juan and Freund-Levi, Yvonne and Frings, Lars
and Guedj, Eric and Habeck, Christian G and Handels, Ron and
Hausner, Lucrezia and Hellwig, Sabine and Jiménez-Bonilla,
Julio F and Juaristi, Ane Iriondo and Kandimalla, Ramesh and
Kern, Silke and Bordewick Kirsebom, Bjørn-Eivind S and
Kornhuber, Johannes and Legdeur, Nienke and Levin, Johannes
and Maier, Wolfgang and Marquié, Marta and Minatani,
Shinobu and Morbelli, Silvia Daniela and Mroczko, Barbara
and Ntanasi, Eva and de Oliveira, Catarina Resende and
Orellana, Adelina and Peters, Oliver and Prabhakar, Sudesh
and Ramakers, Inez H and Rodríguez-Rodriguez, Eloy and
Ruiz, Agustín and Rüther, Eckart and Sakhardande, Jayant
and Selnes, Per and Silva, Dina and Soininen, Hilkka and
Spiru, Luiza and Takeda, Akitoshi and Teunissen, Charlotte E
and Tijms, Betty M and Vermunt, Lisa and Wallin, Åsa K and
Wiels, Wietse and Yannakoulia, Mary and Yi, Dahyun and
Zettergren, Anna and Ossenkoppele, Rik and Verhey, Frans Rj
and Visser, Pieter Jelle and Jansen, Willemijn J},
collaboration = {Initiative, Alzheimer's Disease Neuroimaging and group, A4
Study and Network, Dominantly Inherited Alzheimer and
Dementia, European Prevention of Alzheimer's and Disease,
Prediction of Alzheimer's and Disease, Presymptomatic
Evaluation of Experimental or Novel Treatments for
Alzheimer's and Early Diagnosis},
othercontributors = {Japan Alzheimer's Disease Neuroimaging Initiative , Korean
Brain Aging Study},
title = {{A}ssociations of lifestyle factors with amyloid pathology
in persons without dementia.},
journal = {Journal of Alzheimer's disease},
volume = {108},
number = {3},
issn = {1387-2877},
address = {Amsterdam},
publisher = {IOS Press},
reportid = {DZNE-2025-01322},
pages = {1043 - 1059},
year = {2025},
abstract = {BackgroundThe association between lifestyle factors and
Alzheimer's disease (AD) pathophysiology remains
incompletely understood.ObjectiveThe aim of this study was
to assess the association of alcohol consumption, smoking
behavior, sleep quality and physical, cognitive, and social
activity with cerebral amyloid pathology.MethodsFor this
cross-sectional study, we selected participants from the
Amyloid Biomarker Study data pooling initiative. We used
generalized estimating equations to assess associations of
dichotomized lifestyle measures with amyloid
pathology.ResultsWe included 9171 participants with normal
cognition (NC) and 2555 participants with mild cognitive
impairment (MCI) from the Amyloid Biomarker Study. Of
participants with NC, $58\%$ were women, $34\%$ were APOE
ε4 carrier, and $27\%$ had amyloid pathology. Of
participants with MCI, $48\%$ were women, $47\%$ were APOE
ε4 carrier, and $57\%$ had amyloid pathology. In NC,
cognitively active participants were less likely to have
amyloid pathology (OR = 0.77, $95\%CI$ 0.66-0.89, p <
0.001). In MCI, participants who had ever smoked or had
sleep problems were less likely to have amyloid pathology
(OR = 0.85, $95\%CI$ 0.73-0.99, p = 0.029; OR = 0.62,
$95\%CI$ 0.45-0.86, p = 0.004).ConclusionsIn NC, cognitive
activity was associated with a lower frequency of amyloid
pathology. In MCI, favorable lifestyle behaviors were not
associated with a lower frequency of amyloid pathology. The
results of the current study contribute to the broader
evidence base on lifestyle and AD by further characterizing
the role of lifestyle behaviors in AD pathology across
different clinical stages.},
keywords = {Humans / Female / Male / Aged / Life Style /
Cross-Sectional Studies / Cognitive Dysfunction: pathology /
Cognitive Dysfunction: psychology / Cognitive Dysfunction:
metabolism / Cognitive Dysfunction: genetics / Aged, 80 and
over / Alcohol Drinking / Smoking / Middle Aged / Amyloid:
metabolism / Apolipoprotein E4: genetics / Dementia /
Alzheimer's disease (Other) / amyloid (Other) / amyloid
biomarker study (Other) / cerebrospinal fluid (Other) /
lifestyle (Other) / positron emission tomography (Other) /
Amyloid (NLM Chemicals) / Apolipoprotein E4 (NLM Chemicals)},
cin = {Clinical Research (Munich) / AG Levin},
ddc = {610},
cid = {I:(DE-2719)1111015 / I:(DE-2719)1111016},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41234025},
pmc = {pmc:PMC12647378},
doi = {10.1177/13872877251379083},
url = {https://pub.dzne.de/record/282559},
}