Use of allele scores as instrumental variables for Mendelian randomization

Int J Epidemiol. 2013 Aug;42(4):1134-44. doi: 10.1093/ije/dyt093.


Background: An allele score is a single variable summarizing multiple genetic variants associated with a risk factor. It is calculated as the total number of risk factor-increasing alleles for an individual (unweighted score), or the sum of weights for each allele corresponding to estimated genetic effect sizes (weighted score). An allele score can be used in a Mendelian randomization analysis to estimate the causal effect of the risk factor on an outcome.

Methods: Data were simulated to investigate the use of allele scores in Mendelian randomization where conventional instrumental variable techniques using multiple genetic variants demonstrate 'weak instrument' bias. The robustness of estimates using the allele score to misspecification (for example non-linearity, effect modification) and to violations of the instrumental variable assumptions was assessed.

Results: Causal estimates using a correctly specified allele score were unbiased with appropriate coverage levels. The estimates were generally robust to misspecification of the allele score, but not to instrumental variable violations, even if the majority of variants in the allele score were valid instruments. Using a weighted rather than an unweighted allele score increased power, but the increase was small when genetic variants had similar effect sizes. Naive use of the data under analysis to choose which variants to include in an allele score, or for deriving weights, resulted in substantial biases.

Conclusions: Allele scores enable valid causal estimates with large numbers of genetic variants. The stringency of criteria for genetic variants in Mendelian randomization should be maintained for all variants in an allele score.

Keywords: Mendelian randomization; allele scores; genetic risk scores; instrumental variables; weak instruments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Bias
  • Causality
  • Humans
  • Mendelian Randomization Analysis / methods*
  • Models, Genetic
  • Risk Factors