Abstract

BackgroundTwo-sample Mendelian randomization (MR) allows the use of freely accessible summary association results from genome-wide association studies (GWAS) to estimate causal effects of modifiable exposures on outcomes. Some GWAS adjust for heritable covariables in an attempt to estimate direct effects of genetic variants on the trait of interest. One, both or neither of the exposure GWAS and outcome GWAS may have been adjusted for covariables.MethodsWe performed a simulation study comprising different scenarios that could motivate covariable adjustment in a GWAS and analysed real data to assess the influence of using covariable-adjusted summary association results in two-sample MR.ResultsIn the absence of residual confounding between exposure and covariable, between exposure and outcome, and between covariable and outcome, using covariable-adjusted summary associations for two-sample MR eliminated bias due to horizontal pleiotropy. However, covariable adjustment led to bias in the presence of residual confounding (especially between the covariable and the outcome), even in the absence of horizontal pleiotropy (when the genetic variants would be valid instruments without covariable adjustment). In an analysis using real data from the Genetic Investigation of ANthropometric Traits (GIANT) consortium and UK Biobank, the causal effect estimate of waist circumference on blood pressure changed direction upon adjustment of waist circumference for body mass index.ConclusionsOur findings indicate that using covariable-adjusted summary associations in MR should generally be avoided. When that is not possible, careful consideration of the causal relationships underlying the data (including potentially unmeasured confounders) is required to direct sensitivity analyses and interpret results with appropriate caution.

Highlights

  • Mendelian randomization (MR) uses genetic variants to assess the influence of modifiable exposures on health outcomes.[1,2] As germline genetic variants are generally independent of confounding factors and are determined at conception, MR offers a more robust approach to confounding and reverse causation than other methods used in observational studies.[3]Two-sample MR is an extension to the one-sample MR design, where estimates for the association of genetic variants with exposure and with outcome are derived from different samples from the same underlying population.[4]

  • In an extensive simulation study, we demonstrate that using covariable-adjusted summary associations may bias MR analyses

  • Our findings indicate that using covariable-adjusted summary associations in MR should generally be avoided

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Summary

Introduction

Mendelian randomization (MR) uses genetic variants to assess the influence of modifiable exposures on health outcomes.[1,2] As germline genetic variants are generally independent of confounding factors and are determined at conception, MR offers a more robust approach to confounding and reverse causation than other methods used in observational studies.[3]Two-sample MR is an extension to the one-sample MR design, where estimates for the association of genetic variants with exposure and with outcome are derived from different (non-overlapping) samples from the same underlying population.[4]. In recent years, twosample MR has substantially grown in popularity[6] since it capitalizes on the use of publiclyavailable summary association results from large genome-wide association studies (GWAS). Two-sample Mendelian randomization (MR) allows the use of freely accessible summary association results from genome-wide association studies (GWAS) to estimate causal effects of modifiable exposures on outcomes. Some GWAS adjust for heritable covariables in an attempt to estimate direct effects of genetic variants on the trait of interest. One, both or neither of the exposure GWAS and outcome GWAS may have been adjusted for covariables

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