4.5 Article

Combining information on multiple instrumental variables in Mendelian randomization: comparison of allele score and summarized data methods

Journal

STATISTICS IN MEDICINE
Volume 35, Issue 11, Pages 1880-1906

Publisher

WILEY
DOI: 10.1002/sim.6835

Keywords

Mendelian randomization; weak instruments; instrumental variables; causal inference; genetic variants; summarized data; aggregated data; allele score; genetic risk score

Funding

  1. Wellcome Trust [100114]
  2. Medical Research Council [K006215]
  3. British Heart Foundation [CH/12/2/29428]
  4. British Heart Foundation [RG/08/014/24067, SP/08/007/23628] Funding Source: researchfish
  5. Medical Research Council [MR/K006215/1, MR/L003120/1] Funding Source: researchfish
  6. National Institute for Health Research [NF-SI-0512-10165] Funding Source: researchfish
  7. MRC [MR/K006215/1, MR/L003120/1] Funding Source: UKRI

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Mendelian randomization is the use of genetic instrumental variables to obtain causal inferences from observational data. Two recent developments for combining information on multiple uncorrelated instrumental variables (IVs) into a single causal estimate are as follows: (i) allele scores, in which individual-level data on the IVs are aggregated into a univariate score, which is used as a single IV, and (ii) a summary statistic method, in which causal estimates calculated from each IV using summarized data are combined in an inverse-variance weighted meta-analysis. To avoid bias from weak instruments, unweighted and externally weighted allele scores have been recommended. Here, we propose equivalent approaches using summarized data and also provide extensions of the methods for use with correlated IVs. We investigate the impact of different choices of weights on the bias and precision of estimates in simulation studies. We show that allele score estimates can be reproduced using summarized data on genetic associations with the risk factor and the outcome. Estimates from the summary statistic method using external weights are biased towards the null when the weights are imprecisely estimated; in contrast, allele score estimates are unbiased. With equal or external weights, both methods provide appropriate tests of the null hypothesis of no causal effect even with large numbers of potentially weak instruments. We illustrate these methods using summarized data on the causal effect of low-density lipoprotein cholesterol on coronary heart disease risk. It is shown that a more precise causal estimate can be obtained using multiple genetic variants from a single gene region, even if the variants are correlated. (c) 2015 The Authors. Statistics in Medicine published by John Wiley & Sons Ltd.

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