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Genetic Associations Between Modifiable Risk Factors and Alzheimer Disease

  • Jiao Luo
  • , Jesper Qvist Thomassen
  • , Céline Bellenguez
  • , Benjamin Grenier-Boley
  • , Itziar de Rojas
  • , Atahualpa Castillo
  • , Kayenat Parveen
  • , Fahri Küçükali
  • , Aude Nicolas
  • , Oliver Peters
  • , Anja Schneider
  • , Martin Dichgans
  • , Dan Rujescu
  • , Norbert Scherbaum
  • , Deckert Jürgen
  • , Steffi Riedel-Heller
  • , Lucrezia Hausner
  • , Laura Molina Porcel
  • , Emrah Düzel
  • , Timo Grimmer
  • Jens Wiltfang, Stefanie Heilmann-Heimbach, Susanne Moebus, Thomas Tegos, Nikolaos Scarmeas, Jordi Clarimon, Fermin Moreno, Jordi Pérez-Tur, María J Bullido, Pau Pastor, Raquel Sánchez-Valle, Victoria Álvarez, Mercè Boada, Pablo García-González, Raquel Puerta, Pablo Mir, Luis M Real, Gerard Piñol-Ripoll, Jose María García-Alberca, Jose Luís Royo, Eloy Rodriguez-Rodriguez, Hilkka Soininen, Teemu Kuulasmaa, Alexandre de Mendonça, Shima Mehrabian, Jakub Hort, Martin Vyhnalek, Sven van der Lee, Caroline Graff, Goran Papenberg, Vilmantas Giedraitis, Anne Boland, Delphine Bacq-Daian, Jean-François Deleuze, Gael Nicolas, Carole Dufouil, Florence Pasquier, Olivier Hanon, Stéphanie Debette, Edna Grünblatt, Julius Popp, Luisa Benussi, Daniela Galimberti, Beatrice Arosio, Patrizia Mecocci, Vincenzo Solfrizzi, Lucilla Parnetti, Alessio Squassina, Lucio Tremolizzo, Barbara Borroni, Benedetta Nacmias, Sandro Sorbi, Paolo Caffarra, Davide Seripa, Innocenzo Rainero, Antonio Daniele, Carlo Masullo, Gianfranco Spalletta, Julie Williams, Philippe Amouyel, Frank Jessen, Patrick Kehoe, Tsolaki Magda, Giacomina Rossi, Pascual Sánchez-Juan, Kristel Sleegers, Martin Ingelsson, Ole A Andreassen, Mikko Hiltunen, Cornelia Van Duijn, Rebecca Sims, Wiesje van der Flier, Agustín Ruiz, Alfredo Ramirez, Jean-Charles Lambert, Ruth Frikke-Schmidt*
*Corresponding author
  • University of Copenhagen
  • RID-AGE-Risk Factors and Molecular Determinants of Aging-Related Diseases
  • Cardiff University
  • University of Bonn
  • University of Cologne
  • Berlin Institute of Health
  • German Center for Neurodegenerative Diseases
  • Ludwig Maximilian University of Munich
  • Medical University of Vienna
  • Institutes and Clinics of the University Duisburg-Essen
  • University of Würzburg
  • Leipzig University
  • Heidelberg University 
  • Hematology, Hospital Clínic
  • Otto von Guericke University Magdeburg
  • Technical University of Munich
  • University of Göttingen
  • University of Duisburg-Essen
  • Aristotle University of Thessaloniki
  • Columbia University
  • National and Kapodistrian University of Athens
  • CIBER - Center for Biomedical Research Network
  • Autonomous University of Barcelona
  • Hospital Universitario Donostia
  • Biodonostia Health Research Institute
  • CSIC - Institute of Biomedicine of Valencia
  • Instituto Investigacion Sanitaria la Fe
  • Hospital Germans Trias i Pujol
  • University of Barcelona
  • Hospital Universitario Central de Asturias- Oviedo and Instituto de Investigación Biosanitaria del Principado de Asturias
  • Hospital Universitario Central de Asturias
  • UIC Barcelona
  • Hospital Universitario Virgen del Rocio
  • Hospital Universitari Santa Maria de Lleida
  • Biomedical Research Institute of Lleida
  • University of Málaga
  • Hospital Universitario Marques de Valdecilla
  • University of Eastern Finland
  • Medical University Sofia
  • Masaryk University
  • Charles University
  • Karolinska Institutet
  • Uppsala University
  • Centre National de Recherche en Génomique Humaine
  • FHU G4 Génomique
  • CHU Hôpitaux de Bordeaux
  • Bordeaux Population Health Research Center
  • Université de Lille
  • Hôpital Broca
  • University of Zurich
  • Universität Zürich
  • University of Lausanne
  • IRCCS Centro San Giovanni di Dio Fatebenefratelli - Brescia
  • IRCCS Fondazione Ca'Granda – Ospedale Maggiore Policlinico - Milano
  • University of Milan
  • University of Perugia
  • University of Bari
  • University of Cagliari
  • University of Milan - Bicocca
  • University of Brescia
  • IRCCS Fondazione Don Carlo Gnocchi - Milano
  • University of Florencec
  • University of Parma
  • Ospedale Vito Fazzi
  • University of Turin
  • Baylor College of Medicine
  • IRCCS Fondazione Santa Lucia - Roma
  • Southmead Hospital
  • IRCCS Fondazione Istituto Neurologico Carlo Besta - Milano
  • Centro de Investigación de Enfermedades Neurológicas
  • University of Antwerp
  • University Health Network University of Toronto
  • University of Toronto
  • University of Oxford
  • Erasmus Medical Center
  • University of Texas Health Science Center at San Antonio

Research output: Contribution to journalArticle

Abstract

Importance: An estimated 40% of dementia is potentially preventable by modifying 12 risk factors throughout the life course. However, robust evidence for most of these risk factors is lacking. Effective interventions should target risk factors in the causal pathway to dementia. Objective: To comprehensively disentangle potentially causal aspects of modifiable risk factors for Alzheimer disease (AD) to inspire new drug targeting and improved prevention. Design, setting, and participants: This genetic association study was conducted using 2-sample univariable and multivariable mendelian randomization. Independent genetic variants associated with modifiable risk factors were selected as instrumental variables from genomic consortia. Outcome data for AD were obtained from the European Alzheimer & Dementia Biobank (EADB), generated on August 31, 2021. Main analyses were conducted using the EADB clinically diagnosed end point data. All analyses were performed between April 12 and October 27, 2022. Exposures: Genetically determined modifiable risk factors. Main outcomes and measures: Odds ratios (ORs) and 95% CIs for AD were calculated per 1-unit change of genetically determined risk factors. Results: The EADB-diagnosed cohort included 39 106 participants with clinically diagnosed AD and 401 577 control participants without AD. The mean age ranged from 72 to 83 years for participants with AD and 51 to 80 years for control participants. Among participants with AD, 54% to 75% were female, and among control participants, 48% to 60% were female. Genetically determined high-density lipoprotein (HDL) cholesterol concentrations were associated with increased odds of AD (OR per 1-SD increase, 1.10 [95% CI, 1.05-1.16]). Genetically determined high systolic blood pressure was associated with increased risk of AD after adjusting for diastolic blood pressure (OR per 10-mm Hg increase, 1.22 [95% CI, 1.02-1.46]). In a second analysis to minimize bias due to sample overlap, the entire UK Biobank was excluded from the EADB consortium; odds for AD were similar for HDL cholesterol (OR per 1-SD unit increase, 1.08 [95% CI, 1.02-1.15]) and systolic blood pressure after adjusting for diastolic blood pressure (OR per 10-mm Hg increase, 1.23 [95% CI, 1.01-1.50]). Conclusions and relevance: This genetic association study found novel genetic associations between high HDL cholesterol concentrations and high systolic blood pressure with higher risk of AD. These findings may inspire new drug targeting and improved prevention implementation.
Original languageEnglish
Pages (from-to)353-368
Number of pages16
JournalJAMA network open
Volume6
Issue number5
DOIs
Publication statusPublished - 2023

All Science Journal Classification (ASJC) codes

  • General Medicine

Keywords

  • Alzheimer Disease
  • Genetic Associations
  • Modifiable Risk Factors

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