New Insights into Polygenic Score-Lifestyle Interactions for Cardiometabolic Risk Factors from Genome-Wide Interaction Analyses

Nutrients. 2023 Nov 17;15(22):4815. doi: 10.3390/nu15224815.

Abstract

The relationship between lifestyles and cardiometabolic outcomes varies between individuals. In 382,275 UK Biobank Europeans, we investigate how lifestyles interact with polygenic scores (PGS) of cardiometabolic risk factors. We identify six interactions (PGS for body mass index with meat diet, physical activity, sedentary behaviour and insomnia; PGS for high-density lipoprotein cholesterol with sedentary behaviour; PGS for triglycerides with meat diet) in multivariable linear regression models including an interaction term and show stronger associations between lifestyles and cardiometabolic risk factors among individuals with high PGSs than those with low PGSs. Genome-wide interaction analyses pinpoint three genetic variants (FTO rs72805613 for BMI; CETP rs56228609 for high-density lipoprotein cholesterol; TRIB2 rs4336630 for triglycerides; PInteraction < 5 × 10-8). The associations between lifestyles and cardiometabolic risk factors differ between individuals grouped by the genotype of these variants, with the degree of differences being similar to that between individuals with high and low values for the corresponding PGSs. This study demonstrates that associations between lifestyles and cardiometabolic risk factors can differ between individuals based upon their genetic profiles. It further suggests that genetic variants with interaction effects contribute more to such differences compared to those without interaction effects, which has potential implications for developing PGSs for personalised intervention.

Keywords: BMI; blood lipid; blood pressure; cardiometabolic risk; diet; gene–environment interaction; lifestyle; physical activity; polygenic risk score; polygenic score.

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Cardiometabolic Risk Factors*
  • Cholesterol
  • Humans
  • Lipoproteins, HDL
  • Risk Factors
  • Sedentary Behavior*
  • Triglycerides

Substances

  • Triglycerides
  • Lipoproteins, HDL
  • Cholesterol
  • TRIB2 protein, human
  • Calcium-Calmodulin-Dependent Protein Kinases
  • FTO protein, human
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO

Grants and funding

This research received no external funding.