Machine learning in Alzheimer's disease genetics

  • Matthew Bracher-Smith
  • , Federico Melograna
  • , Brittany Ulm
  • , Céline Bellenguez
  • , Benjamin Grenier-Boley
  • , Diane Duroux
  • , Alejo J Nevado
  • , Peter Holmans
  • , Betty M Tijms
  • , Marc Hulsman
  • , Itziar de Rojas
  • , Rafael Campos-Martin
  • , Sven van der Lee
  • , Atahualpa Castillo
  • , Fahri Küçükali
  • , Oliver Peters
  • , Anja Schneider
  • , Martin Dichgans
  • , Dan Rujescu
  • , Norbert Scherbaum
  • Jürgen Deckert, Steffi Riedel-Heller, Lucrezia Hausner, Laura Molina-Porcel, Emrah Düzel, Timo Grimmer, Jens Wiltfang, Stefanie Heilmann-Heimbach, Susanne Moebus, Thomas Tegos, Nikolaos Scarmeas, Oriol Dols-Icardo, 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, Eloy Rodriguez-Rodriguez, Hilkka Soininen, Sami Heikkinen, Alexandre de Mendonça, Shima Mehrabian, EADB, Frans Verhey, Kristel Van Steen*, Cornelia M. van Duijn*, Valentina Escott-Price*, Inez Ramakers
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Traditional statistical approaches have advanced our understanding of the genetics of complex diseases, yet are limited to linear additive models. Here we applied machine learning (ML) to genome-wide data from 41,686 individuals in the largest European consortium on Alzheimer's disease (AD) to investigate the effectiveness of various ML algorithms in replicating known findings, discovering novel loci, and predicting individuals at risk. We utilised Gradient Boosting Machines (GBMs), biological pathway-informed Neural Networks (NNs), and Model-based Multifactor Dimensionality Reduction (MB-MDR) models. ML approaches successfully captured all genome-wide significant genetic variants identified in the training set and 22% of associations from larger meta-analyses. They highlight 6 novel loci which replicate in an external dataset, including variants which map to ARHGAP25, LY6H, COG7, SOD1 and ZNF597. They further identify novel association in AP4E1, refining the genetic landscape of the known SPPL2A locus. Our results demonstrate that machine learning methods can achieve predictive performance comparable to classical approaches in genetic epidemiology and have the potential to uncover novel loci that remain undetected by traditional GWAS. These insights provide a complementary avenue for advancing the understanding of AD genetics.
Original languageEnglish
Article number6726
Pages (from-to)6726
JournalNature Communications
Volume16
Issue number1
DOIs
Publication statusPublished - 22 Jul 2025

Keywords

  • Alzheimer Disease/genetics
  • Humans
  • Machine Learning
  • Genome-Wide Association Study
  • Genetic Predisposition to Disease
  • Polymorphism, Single Nucleotide
  • Algorithms
  • GTPase-Activating Proteins/genetics
  • Neural Networks, Computer

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