Correcting for effect modification in the doubly-ranked non-linear Mendelian randomization method
Year: 2026
Type: preprint
Abstract: The doubly-ranked non-linear Mendelian randomization method can yield biased estimates when instrument strength varies across individuals due to gene-environment (GxE) interactions. We propose a simple strategy to mitigate this bias by modelling GxE interactions and removing the fitted GxE component from the exposure before stratification by the doubly-ranked method. In simulations, the proposed GxE correction strategy eliminated GxE-induced bias with null, linear and non-linear exposure-outcome relationships, and it did not introduce bias even when the effect modifier of the IV-exposure association was a confounder or was correlated with a mediator or collider of the exposure-outcome association. In empirical analyses of serum 25(OH)D, BMI, and LDL-C, falsification tests showed bias in the uncorrected doubly-ranked method. Under the selected panel of effect modifiers, the extent of bias attenuation achieved by GxE correction varied by exposures. GxE correction was most effective for LDL-C, with further support from analyses using negative controls (age at recruitment and sex) and coronary artery disease as a positive control. These findings provide proof of principle evidence that our proposed GxE correction strategy can mitigate GxE-induced bias in practice. Where applicable, we recommend implementing this GxE correction strategy as a sensitivity analysis to assess the robustness of findings from the doubly-ranked method.
Source: medRxiv
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Funders: Wellcome Trust, Scottish Government, National Institute for Health and Care Research, British Heart Foundation, Department of Health and Social Care, Public Health Agency, Chief Scientist Office, Scottish Government Health and Social Care Directorate, Medical Research Council, Engineering and Physical Sciences Research Council, Economic and Social Research Council, Health and Social Care Research and Development Division, NIHR Cambridge Biomedical Research Centre
OpenAlex ID: W7125600566
