Quantification of the overall contribution of gene-environment interaction for obesity-related traits.
Jonathan SulcNinon MounierFelix GuentherThomas W WinklerAndrew R WoodTimothy M FraylingIris M HeidMatthew R RobinsonZoltán KutalikPublished in: Nature communications (2020)
The growing sample size of genome-wide association studies has facilitated the discovery of gene-environment interactions (GxE). Here we propose a maximum likelihood method to estimate the contribution of GxE to continuous traits taking into account all interacting environmental variables, without the need to measure any. Extensive simulations demonstrate that our method provides unbiased interaction estimates and excellent coverage. We also offer strategies to distinguish specific GxE from general scale effects. Applying our method to 32 traits in the UK Biobank reveals that while the genetic risk score (GRS) of 376 variants explains 5.2% of body mass index (BMI) variance, GRSxE explains an additional 1.9%. Nevertheless, this interaction holds for any variable with identical correlation to BMI as the GRS, hence may not be GRS-specific. Still, we observe that the global contribution of specific GRSxE to complex traits is substantial for nine obesity-related measures (including leg impedance and trunk fat-free mass).
Keyphrases
- genome wide
- body mass index
- weight gain
- copy number
- dna methylation
- insulin resistance
- metabolic syndrome
- genome wide association
- weight loss
- type diabetes
- adipose tissue
- small molecule
- high fat diet induced
- magnetic resonance imaging
- magnetic resonance
- risk assessment
- high throughput
- transcription factor
- computed tomography
- fatty acid
- skeletal muscle
- lower limb
- single cell
- affordable care act
- health insurance
- genome wide analysis
- monte carlo