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Associations of lifestyle factors with amyloid pathology in persons without dementia

  • Julie E. Oomens*
  • , Stephanie J. B. Vos
  • , Nancy N. Maserejian
  • , Mercè Boada
  • , Mira Didic
  • , Sebastiaan Engelborghs
  • , Tormod Fladby
  • , Wiesje M. van der Flier
  • , Giovanni B. Frisoni
  • , Lutz Fröhlich
  • , Kiran Dip Gill
  • , Timo Grimmer
  • , Jakub Hort
  • , Yoshiaki Itoh
  • , Takeshi Iwatsubo
  • , Aleksandra Klimkowicz-Mrowiec
  • , Susan M. Landau
  • , Dong Young Lee
  • , Alberto Lleó
  • , Pablo Martinez-Lage
  • Alexandre de Mendonça, Philipp T. Meyer, Piero Parchi, Matteo Pardini, Lucilla Parnetti, Julius Popp, Lorena Rami, Eric M. Reiman, Juha O. Rinne, Karen M. Rodrigue, Pascual Sánchez-Juan, Isabel Santana, Nikolaos Scarmeas, Philip Scheltens, Ingmar Skoog, Reisa A. Sperling, Yaakov Stern, Sylvia Villeneuve, Gunhild Waldemar, Jens Wiltfang, Henrik Zetterberg, Daniel Alcolea, Ricardo F. Allegri, Daniele Altomare, Randall J. Bateman, Simone Baiardi, Ines Baldeiras, Kaj Blennow, Anouk den Braber, Mark A. van Buchem, Min Soo Byun, Jiří Cerman, Kewei Chen, Elena Chipi, Gregory S. Day, Alexander Drzezga, Laura L. Ekblad, Stefan Förster, Juan Fortea, Yvonne Freund-Levi, Lars Frings, Eric Guedj, Christian G. Habeck, Ron Handels, Lucrezia Hausner, Sabine Hellwig, Julio F. Jiménez-Bonilla, Ane Iriondo Juaristi, Ramesh Kandimalla, Silke Kern, Bjørn-Eivind S. Bordewick Kirsebom, Johannes Kornhuber, Nienke Legdeur, Johannes Levin, Wolfgang Maier, Marta Marquié, Shinobu Minatani, Silvia Daniela Morbelli, Barbara Mroczko, Eva Ntanasi, Catarina Resende de Oliveira, Adelina Orellana, Oliver Peters, Sudesh Prabhakar, Inez H. Ramakers, Eloy Rodríguez-Rodriguez, Agustín Ruiz, Eckart Rüther, Jayant Sakhardande, Per Selnes, Dina Silva, Hilkka Soininen, Luiza Spiru, Akitoshi Takeda, Alzheimer’s Disease Neuroimaging Initiative (ADNI), A4 Study group, Dominantly Inherited Alzheimer Network (DIAN), European Prevention of Alzheimer's Dementia (EPAD) consortium, Fundació ACE Healthy Brain Initiative (FACEHBI), Japan Alzheimer's Disease Neuroimaging Initiative (J-ADNI), Korean Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer's Disease (KBASE), Presymptomatic Evaluation of Experimental or Novel Treatments for Alzheimer's Disease (PREVENT-AD) research group
*Corresponding author for this work
  • Maastricht University
  • Biogen IDEC
  • UIC Barcelona
  • Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas
  • Hopital La Timone
  • Institut de Neurosciences des Systèmes
  • University of Antwerp
  • Vrije Universiteit Brussel
  • University of Oslo
  • Vrije Universiteit Amsterdam
  • University of Geneva
  • Heidelberg University 
  • Postgraduate Institute of Medical Education and Research
  • Technical University of Munich
  • Charles University
  • Osaka Metropolitan University
  • The University of Tokyo
  • Jagiellonian University Medical College
  • University of California at Berkeley
  • Seoul National University
  • Hospital de Sant Pau
  • Center for Research and Advanced Therapies
  • University of Lisbon
  • University of Freiburg
  • IRCCS Istituto delle Scienze Neurologiche di Bologna
  • University of Bologna
  • University of Genoa
  • University of Perugia
  • University of Zurich
  • University of Lausanne
  • Hospital Clinic de Barcelona
  • Banner Health
  • University of Turku
  • University of Texas at Dallas
  • CIEN Tissue Bank, Alzheimer’s Centre Reina Sofía-CIEN Foundation
  • University of Coimbra
  • National and Kapodistrian University of Athens
  • Columbia University
  • University of Gothenburg
  • Harvard University
  • McGill University
  • Institut Universitaire en Santé Mentale Douglas
  • University of Copenhagen
  • University of Göttingen
  • University of Tübingen
  • Sahlgrenska University Hospital
  • University College London
  • UK Dementia Research Institute
  • Hong Kong Center for Neurodegenerative Diseases
  • University of Wisconsin-Madison
  • Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia
  • University of Brescia
  • Washington University St. Louis
  • Leiden University
  • Mayo Clinic Jacksonville, FL
  • University of Cologne
  • Klinikum Bayreuth GmbH
  • Örebro University
  • Karolinska Institutet
  • King's College London
  • Institut Fresnel
  • Hospital Universitario Marques de Valdecilla
  • Emory University
  • CSIR - Indian Institute of Chemical Technology
  • Mahatma Gandhi Memorial Hospital
  • University Hospital of North Norway
  • University of Tromsø – The Arctic University of Norway
  • Friedrich-Alexander University Erlangen-Nürnberg
  • Ludwig Maximilian University of Munich
  • German Center for Neurodegenerative Diseases
  • Munich Cluster for Systems Neurology (SyNergy)
  • University of Bonn
  • IRCCS San Martino Polyclinic Hospital
  • Medical University of Białystok
  • Harokopio University
  • Charité – Universitätsmedizin Berlin
  • University of Eastern Finland
  • Carol Davila University of Medicine and Pharmacy
  • Ana Aslan International Academy of Aging
  • Lund University
  • OLV Hospital Aalst

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background: The association between lifestyle factors and Alzheimer's disease (AD) pathophysiology remains incompletely understood. Objective: The 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. Methods: For 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. Results: We 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). Conclusions: In 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.

Original languageEnglish
Pages (from-to)1043-1059
Number of pages17
JournalJ. Alzheimer's Dis.
Volume108
Issue number3
DOIs
Publication statusPublished - 1 Dec 2025

Keywords

  • Alzheimer's disease
  • amyloid
  • amyloid biomarker study
  • cerebrospinal fluid
  • lifestyle
  • positron emission tomography

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