AI Article Synopsis

  • - The study discusses the evolution of polygenic risk score (PRS) models in genetics, emphasizing how genotype-environment interaction (GxE) influences the effectiveness of these models, particularly noting the issues with current GxE PRS applications that can lead to errors.
  • - New GxE PRS models are proposed that improve upon existing methods by including both additive and interactive genetic effects along with a quadratic term for nongenetic factors, which enhances their reliability in predicting complex traits.
  • - The research demonstrates through simulations and real-world data that these new models more effectively manage type 1 error rates and reveal significant GxE effects on traits such as body mass index and hypertension, culminating in the development of a specialized R

Article Abstract

The use of polygenic risk score (PRS) models has transformed the field of genetics by enabling the prediction of complex traits and diseases based on an individual's genetic profile. However, the impact of genotype-environment interaction (GxE) on the performance and applicability of PRS models remains a crucial aspect to be explored. Currently, existing genotype-environment interaction polygenic risk score (GxE PRS) models are often inappropriately used, which can result in inflated type 1 error rates and compromised results. In this study, we propose novel GxE PRS models that jointly incorporate additive and interaction genetic effects although also including an additional quadratic term for nongenetic covariates, enhancing their robustness against model misspecification. Through extensive simulations, we demonstrate that our proposed models outperform existing models in terms of controlling type 1 error rates and enhancing statistical power. Furthermore, we apply the proposed models to real data, and report significant GxE effects. Specifically, we highlight the impact of our models on both quantitative and binary traits. For quantitative traits, we uncover the GxE modulation of genetic effects on body mass index by alcohol intake frequency. In the case of binary traits, we identify the GxE modulation of genetic effects on hypertension by waist-to-hip ratio. These findings underscore the importance of employing a robust model that effectively controls type 1 error rates, thus preventing the occurrence of spurious GxE signals. To facilitate the implementation of our approach, we have developed an innovative R software package called GxEprs, specifically designed to detect and estimate GxE effects. Overall, our study highlights the importance of accurate GxE modeling and its implications for genetic risk prediction, although providing a practical tool to support further research in this area.

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Source
http://dx.doi.org/10.1002/gepi.22546DOI Listing

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