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Updated: Jan 30, 2026

Gene-environment Interaction Models to Unmask Susceptibility Mechanisms in Parkinson's Disease
Published on: January 7, 2014
A cross-population compendium of gene-environment interactions
Shinichi Namba1,2,3, Kyuto Sonehara4,5,6, Yuriko N Koyanagi7
1Department of Genome Informatics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. snamba@m.u-tokyo.ac.jp.
None:
Environmental differences in genetic effect sizes, namely, gene-environment interactions, may uncover the genetic encoding of phenotypic plasticity1-3. We provide a cross-population atlas of gene-environment interactions comprising 440,210 individuals from European and Japanese populations, with replication in 539,794 individuals from diverse populations. By decomposing the contributions from age, sex and lifestyles, we delineate the aetiology of these gene-environment interactions, including a reverse-causality from a disease-related dietary change. Genome-wide analyses uncovered missing heritability and trait-trait relationships connected by the synergistic effects of genome and environments, which systematically affected polygenic prediction accuracy and cross-population portability. Single-cell projection revealed aging shift of pathways and cell types responsible for genetic regulation. Omics-level gene-environment analyses identified multiple sex-discordant genetic effects in lipid metabolism, informing clinical trial failures for genetically supported drug development. Our comprehensive gene-environment study decodes the dynamics of genetic associations, offering insights into complex trait biology, personalized medicine and drug development.
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