The Multivariate SEM-PGS Model: Using Polygenic Scores to Investigate Cross-Trait Genetic Nurture and Assortative Mating

Genetic nurture effects and assortative mating (AM) occur across many human behaviors and can bias estimates from traditional genetic models. These influences are typically studied univariately, within the same trait. However, estimation of cross-trait genetic nurture effects and cross-trait AM remains underexplored due to the absence of suitable approaches. To address this, we developed a multivariate extension of the SEM-PGS model for datasets with genotyped and phenotyped parents and offspring, enabling joint estimation of within-trait and cross-trait genetic and environmental influences. By integrating haplotypic polygenic scores (PGS) into a structural equation modeling framework, the model simultaneously estimates same-trait and cross-trait direct effects, genetic nurture, vertical transmission, and assortative mating. We also provide the first formal description of how copaths can be used to model multivariate assortative mating and derive the corresponding parameter expectations in matrix form. Forward-time Monte Carlo simulations under varying conditions of r^2_PGS and N_trio demonstrate that the model yields unbiased estimates of both within-trait and cross-trait effects when assumptions are met. The precision of estimates was adequate with large sample sizes (N_trio > 16k) and improved as PGS predictive power increased. In addition, our simulation results show that failing to model cross-trait effects biases within-trait estimates, underscoring the importance of incorporating cross-trait effects. The multivariate SEM-PGS model offers a powerful and flexible tool for disentangling gene-environment interplay and advancing the understanding of familial influences on human traits.

Publication Details

Journal
ArXiv.org
Published
2025-09-30
Primary Topic
Down syndrome and intellectual disability research
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article

The Multivariate SEM-PGS Model: Using Polygenic Scores to Investigate Cross-Trait Genetic Nurture and Assortative Mating

ArXiv.org
Down syndrome and intellectual disability research
article

The Multivariate SEM-PGS Model: Using Polygenic Scores to Investigate Cross-Trait Genetic Nurture and Assortative Mating

article en

Abstract

Genetic nurture effects and assortative mating (AM) occur across many human behaviors and can bias estimates from traditional genetic models. These influences are typically studied univariately, within the same trait. However, estimation of cross-trait genetic nurture effects and cross-trait AM remains underexplored due to the absence of suitable approaches. To address this, we developed a multivariate extension of the SEM-PGS model for datasets with genotyped and phenotyped parents and offspring, enabling joint estimation of within-trait and cross-trait genetic and environmental influences. By integrating haplotypic polygenic scores (PGS) into a structural equation modeling framework, the model simultaneously estimates same-trait and cross-trait direct effects, genetic nurture, vertical transmission, and assortative mating. We also provide the first formal description of how copaths can be used to model multivariate assortative mating and derive the corresponding parameter expectations in matrix form. Forward-time Monte Carlo simulations under varying conditions of r^2_PGS and N_trio demonstrate that the model yields unbiased estimates of both within-trait and cross-trait effects when assumptions are met. The precision of estimates was adequate with large sample sizes (N_trio > 16k) and improved as PGS predictive power increased. In addition, our simulation results show that failing to model cross-trait effects biases within-trait estimates, underscoring the importance of incorporating cross-trait effects. The multivariate SEM-PGS model offers a powerful and flexible tool for disentangling gene-environment interplay and advancing the understanding of familial influences on human traits.

ArXiv.org
Openalex Percentile: Top 36%
Down syndrome and intellectual disability research
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