Contextualizing selection bias in Mendelian randomization: how bad is it likely to be? - PubMed (original) (raw)
Contextualizing selection bias in Mendelian randomization: how bad is it likely to be?
Apostolos Gkatzionis et al. Int J Epidemiol. 2019.
Abstract
Background: Selection bias affects Mendelian randomization investigations when selection into the study sample depends on a collider between the genetic variant and confounders of the risk factor-outcome association. However, the relative importance of selection bias for Mendelian randomization compared with other potential biases is unclear.
Methods: We performed an extensive simulation study to assess the impact of selection bias on a typical Mendelian randomization investigation. We considered inverse probability weighting as a potential method for reducing selection bias. Finally, we investigated whether selection bias may explain a recently reported finding that lipoprotein(a) is not a causal risk factor for cardiovascular mortality in individuals with previous coronary heart disease.
Results: Selection bias had a severe impact on bias and Type 1 error rates in our simulation study, but only when selection effects were large. For moderate effects of the risk factor on selection, bias was generally small and Type 1 error rate inflation was not considerable. Inverse probability weighting ameliorated bias when the selection model was correctly specified, but increased bias when selection bias was moderate and the model was misspecified. In the example of lipoprotein(a), strong genetic associations and strong confounder effects on selection mean the reported null effect on cardiovascular mortality could plausibly be explained by selection bias.
Conclusions: Selection bias can adversely affect Mendelian randomization investigations, but its impact is likely to be less than other biases. Selection bias is substantial when the effects of the risk factor and confounders on selection are particularly large.
Keywords: causal inference; collider bias; instrumental variables; inverse probability weighting; selection bias.
© The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association.
Figures
Figure 1.
Directed acyclic graphs (DAG) indicating the relationships between an instrumental variable (G), exposure (X), confounder (U) and outcome (Y). Selection (S) leads to bias if it is a function of the exposure (left panel) or the outcome (right panel), as both exposure and outcome are causally downstream of the genetic variant and confounder, and hence conditioning on selection induces an association between the genetic variant and confounder in both cases.
References
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- 204623/Z/16/Z/WT_/Wellcome Trust/United Kingdom
- RG/13/13/30194/BHF_/British Heart Foundation/United Kingdom
- RG88311/MRC_/Medical Research Council/United Kingdom
- MC_UU_00002/7/MRC_/Medical Research Council/United Kingdom
- MR/L003120/1/MRC_/Medical Research Council/United Kingdom
- MR/N027493/1/MRC_/Medical Research Council/United Kingdom
- WT_/Wellcome Trust/United Kingdom
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