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medRxivGenetic & Genomic MedicinePreprint

Disentangling phenotype scale, amplification, and effect heterogeneity underlying polygenic GxE architecture of complex traits

Zhengtong LiuiD, Aakarsh AnandiD, Xinyue Qie, Manuela CostantinoiD, Moonseong 정문성Jeong, Aditya GorlaiD, Noah ZaitleniD, Andy W. DahliD, Sriram SankararamaniD

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Abstract

While polygenic gene-by-environment (GxE) signals are increasingly detected in biobank data, it is often unclear whether they reflect the phenotypes measurement scale or one of two biologically distinct mechanisms: heterogeneous genetic effects across environmental strata (effect heterogeneity) or systematically larger but correlated effects in one stratum (amplification). We introduce REGENA (Robust Estimator of Gene-ENvironment Architectures), a variance-component method that disentangles these contributions at biobank scale by learning a phenotype transformation that minimizes scale-induced GxE, thereby assessing scale-dependence while jointly estimating the cross-environment genetic correlation and environment-specific genetic variances. In simulations, REGENA is well-calibrated and powerful while recovering the transformation underlying scale-dependent GxE. Applied to 43 quantitative traits and seven environmental exposures in 291,273 UK Biobank individuals, REGENA finds that roughly half of trait-environment pairs with significant GxE are scale-dependent. Among the remaining scale-independent trait-environment pairs, GxE heritability accounted for an average of 15% of additive heritability and was driven primarily by effect heterogeneity (accounting for 71% of GxE heritability on average) although there was substantial variation in its relative contribution across trait-environment pairs. Environment-specific effects tend to make a larger contribution at lower allele frequencies, accounting for 6% of genetic variance in low-frequency variants versus 3.9% at common variants (signed test p = 1.7 x 10-24). Modeling these distinctions improves environment-specific polygenic prediction (14% on average), with the largest gains for pairs whose genetic effects are least correlated across environments (p = 4.0 x 10-3; 3.8-fold for testosterone stratified by sex and 2.32-fold for waist-hip ratio stratified by alcohol consumption). Further, environment-stratified GWAS detects 174 loci missed by pooled GWAS with 67 having opposite-signed effects across strata.

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