Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions

Int J Epidemiol. 2019 Jun 1;48(3):702-712. doi: 10.1093/ije/dyy204.

Abstract

Background: Mendelian randomization (MR) has developed into an established method for strengthening causal inference and estimating causal effects, largely due to the proliferation of genome-wide association studies. However, genetic instruments remain controversial, as horizontal pleiotropic effects can introduce bias into causal estimates. Recent work has highlighted the potential of gene-environment interactions in detecting and correcting for pleiotropic bias in MR analyses.

Methods: We introduce MR using Gene-by-Environment interactions (MRGxE) as a framework capable of identifying and correcting for pleiotropic bias. If an instrument-covariate interaction induces variation in the association between a genetic instrument and exposure, it is possible to identify and correct for pleiotropic effects. The interpretation of MRGxE is similar to conventional summary MR approaches, with a particular advantage of MRGxE being the ability to assess the validity of an individual instrument.

Results: We investigate the effect of adiposity, measured using body mass index (BMI), upon systolic blood pressure (SBP) using data from the UK Biobank and a single weighted allelic score informed by data from the GIANT consortium. We find MRGxE produces findings in agreement with two-sample summary MR approaches. Further, we perform simulations highlighting the utility of the approach even when the MRGxE assumptions are violated.

Conclusions: By utilizing instrument-covariate interactions in MR analyses implemented within a linear-regression framework, it is possible to identify and correct for horizontal pleiotropic bias, provided the average magnitude of pleiotropy is constant across interaction-covariate subgroups.

Keywords: MRGxE; Mendelian randomization; gene–environment interaction; invalid instruments; pleiotropy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiposity / genetics*
  • Bias
  • Biological Specimen Banks
  • Blood Pressure / genetics*
  • Body Mass Index
  • Computer Simulation
  • Gene-Environment Interaction*
  • Genetic Pleiotropy
  • Humans
  • Mendelian Randomization Analysis*
  • Obesity / epidemiology*
  • Obesity / genetics