RT Journal Article
SR Electronic
T1 Phenome-scale causal network discovery with bidirectional mediated Mendelian randomization
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.06.18.160176
DO 10.1101/2020.06.18.160176
A1 Brielin C. Brown
A1 David A. Knowles
YR 2020
UL http://biorxiv.org/content/early/2020/06/20/2020.06.18.160176.abstract
AB Inference of directed biological networks from observational genomics datasets is a crucial but notoriously difficult challenge. Modern population-scale biobanks, containing simultaneous measurements of traits, biomarkers and genetic variation, offer unprecedented opportunity to study biological networks. Mendelian randomization (MR) has received attention as a class of methods for inferring causal effects in observational data that uses genetic variants (SNPs) as instrumental variables, but MR methods rely on assumptions that limit their application to complex traits at the biobank-scale. Moreover, MR estimates the total effect of one trait on another, which may be mediated by other factors. Biobanks allow simultaneous measurement of possible mediators, in principle enabling the conversion of MR estimates into direct effects representing a causal network. Here, we show that this can be accomplished by a flexible two stage procedure we call bidirectional mediated Mendelian randomization (bimmer). First, estimate the effect of every trait on every other. Next, approximately invert the resulting matrix. We introduce novel methods for both steps and show via extensive simulations that bimmer is able to learn causal network structures even in the presence of non-causal genetic correlation. We apply bimmer to 405 phenotypes from the UK biobank and demonstrate that learning the network structure is invaluable for interpreting the results of phenome-wide MR, while lending causal support to several recent observational studies.Competing Interest StatementThe authors have declared no competing interest.