Your browser doesn't support javascript.
loading
Mitigating type 1 error inflation and power loss in GxE PRS: Genotype-environment interaction in polygenic risk score models.
Jayasinghe, Dovini; Momin, Md Moksedul; Beckmann, Kerri; Hyppönen, Elina; Benyamin, Beben; Lee, S Hong.
Afiliación
  • Jayasinghe D; Australian Centre for Precision Health, University of South Australia, Adelaide, South Australia, Australia.
  • Momin MM; UniSA Allied Health and Human Performance, University of South Australia, Adelaide, South Australia, Australia.
  • Beckmann K; South Australian Health and Medical Research Institute (SAHMRI), University of South Australia, Adelaide, South Australia, Australia.
  • Hyppönen E; Australian Centre for Precision Health, University of South Australia, Adelaide, South Australia, Australia.
  • Benyamin B; UniSA Allied Health and Human Performance, University of South Australia, Adelaide, South Australia, Australia.
  • Lee SH; South Australian Health and Medical Research Institute (SAHMRI), University of South Australia, Adelaide, South Australia, Australia.
Genet Epidemiol ; 48(2): 85-100, 2024 03.
Article en En | MEDLINE | ID: mdl-38303123
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.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interacción Gen-Ambiente / Puntuación de Riesgo Genético Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interacción Gen-Ambiente / Puntuación de Riesgo Genético Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Australia