Abstract

Body mass index (BMI) is a highly heritable polygenic trait. It is also affected by various environmental and behavioral risk factors. We used a BMI polygenic risk score (PRS) to study the interplay between the genetic and environmental factors defining BMI. First, we generated a BMI PRS that explained more variance than a BMI genetic risk score (GRS), which was using only genome-wide significant BMI-associated variants (R2 = 13.1% compared to 6.1%). Second, we analyzed interactions between BMI PRS and seven environmental factors. We found a significant interaction between physical activity and BMI PRS, even when the well-known effect of the FTO region was excluded from the PRS, using a small dataset of 6,179 samples. Third, we stratified the study population into two risk groups using BMI PRS. The top 22% of the studied populations were included in a high PRS risk group. Engagement in self-reported physical activity was associated with a 1.66 kg/m2 decrease in BMI in this group, compared to a 0.84 kg/m2 decrease in BMI in the rest of the population. Our results (i) confirm that genetic background strongly affects adult BMI in the general population, (ii) show a non-linear interaction between BMI genetics and physical activity, and (iii) provide a standardized framework for future gene-environment interaction analyses.

Highlights

  • Body mass index (BMI) is a complex measure that has been robustly associated with cardiometabolic traits and diseases [1]

  • We investigated the interactions of a BMI polygenic risk score (PRS) with environmental and lifestyle risk factors and used the interaction to develop a criterion for stratifying a population into two risk groups

  • We have detected a non-linear interaction between BMI genetics and physical activity using BMI PRS

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Summary

Introduction

Body mass index (BMI) is a complex measure that has been robustly associated with cardiometabolic traits and diseases [1]. BMI is a highly heritable complex trait, with heritability estimated to be between 30–40% [2,3,4,5]. Studying how genetic variation affects BMI is important to understand the biology of BMI-related diseases. Genome-wide association studies (GWAS) have identified a multitude of BMI-associated genetic variants at the genome-wide significance threshold (p < 5 x 10−8).

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