4.5 Article

Testing and correcting for weak and pleiotropic instruments in two-sample multivariable Mendelian randomization

期刊

STATISTICS IN MEDICINE
卷 40, 期 25, 页码 5434-5452

出版社

WILEY
DOI: 10.1002/sim.9133

关键词

Cochran's Q-statistic; instrument strength; instrument validity; multivariable Mendelian randomization; two-sample Mendelian randomization

资金

  1. Wellcome Trust [108902/B/15/Z]
  2. Medical Research Council [MC_UU_00011/1, MC_UU_00011/2]
  3. MRC [MC_PC_19009] Funding Source: UKRI
  4. Wellcome Trust [108902/B/15/Z] Funding Source: Wellcome Trust

向作者/读者索取更多资源

The text introduces a new method for Multivariable Mendelian randomization (MVMR) to address challenges in estimating causal effects. This method uses a conditional F-statistic to test whether genetic variants strongly predict each exposure, allowing for reliable causal effect estimates in the presence of weak instruments and pleiotropy.
Multivariable Mendelian randomization (MVMR) is a form of instrumental variable analysis which estimates the direct effect of multiple exposures on an outcome using genetic variants as instruments. Mendelian randomization and MVMR are frequently conducted using two-sample summary data where the association of the genetic variants with the exposures and outcome are obtained from separate samples. If the genetic variants are only weakly associated with the exposures either individually or conditionally, given the other exposures in the model, then standard inverse variance weighting will yield biased estimates for the effect of each exposure. Here, we develop a two-sample conditional F-statistic to test whether the genetic variants strongly predict each exposure conditional on the other exposures included in a MVMR model. We show formally that this test is equivalent to the individual level data conditional F-statistic, indicating that conventional rule-of-thumb critical values of F> 10, can be used to test for weak instruments. We then demonstrate how reliable estimates of the causal effect of each exposure on the outcome can be obtained in the presence of weak instruments and pleiotropy, by repurposing a commonly used heterogeneity Q-statistic as an estimating equation. Furthermore, the minimized value of this Q-statistic yields an exact test for heterogeneity due to pleiotropy. We illustrate our methods with an application to estimate the causal effect of blood lipid fractions on age-related macular degeneration.

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