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Bias and mean squared error in Mendelian randomization with invalid instrumental variables
1School of Statistics and Data Science, Nankai University, Tianjin, China.
Abstract:
Mendelian randomization (MR) is a statistical method that utilizes genetic variants as instrumental variables (IVs) to investigate causal relationships between risk factors and outcomes. Although MR has gained popularity in recent years due to its ability to analyze summary statistics from genome-wide association studies (GWAS), it requires a substantial number of single nucleotide polymorphisms (SNPs) as IVs to ensure sufficient power for detecting causal effects. Unfortunately, the complex genetic heritability of many traits can lead to the use of invalid IVs that affect both the risk factor and the outcome directly or through an unobserved confounder. This can result in biased and imprecise estimates, as reflected by a larger mean squared error (MSE). In this study, we focus on the widely used two-stage least squares (2SLS) method and derive formulas for its bias and MSE when estimating causal effects using invalid IVs. Using those formulas, we identify conditions under which the 2SLS estimate is unbiased and reveal how the independent or correlated pleiotropic effects influence the accuracy and precision of the 2SLS estimate. We validate these formulas through extensive simulation studies and demonstrate the application of those formulas in an MR study to evaluate the causal effect of the waist-to-hip ratio on various sleeping patterns. Our results can aid in designing future MR studies and serve as benchmarks for assessing more sophisticated MR methods.
Insights
Mendelian randomization (MR) uses genetic variants to infer causality. This study provides formulas to assess bias and mean squared error (MSE) from invalid instrumental variables (IVs) in two-stage least squares (2SLS) MR analysis.
Area of Science:
- Genetics
- Epidemiology
- Biostatistics
Background:
- Mendelian randomization (MR) is a popular causal inference method using genetic variants as instrumental variables (IVs).
- MR relies on numerous single nucleotide polymorphisms (SNPs) as IVs for statistical power, but invalid IVs can bias results.
- Invalid IVs, due to pleiotropy or confounding, inflate the mean squared error (MSE) of causal effect estimates.
Purpose of the Study:
- To derive formulas for bias and MSE in two-stage least squares (2SLS) MR when using invalid IVs.
- To identify conditions for unbiased 2SLS estimates and analyze the impact of pleiotropic effects on accuracy and precision.
- To validate derived formulas via simulations and apply them to a real-world MR study.
Main Methods:
- Derivation of analytical formulas for bias and MSE of 2SLS estimates with invalid IVs.
- Extensive simulation studies to validate the derived formulas under various scenarios.
- Application of the formulas in a Mendelian randomization study investigating the causal effect of waist-to-hip ratio on sleep patterns.
Main Results:
- Formulas quantifying bias and MSE for 2SLS in the presence of invalid IVs were derived.
- Conditions for unbiased 2SLS estimates were identified, clarifying the influence of pleiotropic effects.
- Simulation studies confirmed the accuracy of the derived formulas, and the application demonstrated their utility in a real-world MR analysis.
Conclusions:
- The derived formulas provide a theoretical framework for understanding bias and precision in 2SLS MR with invalid IVs.
- These results aid in designing more robust MR studies and offer benchmarks for evaluating advanced MR methodologies.
- The study enhances the reliability of causal inference in genetic epidemiology by addressing the challenge of invalid instrumental variables.
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