Pseudo-Sibship Methods in the Case-Parents Design

摘要

Recent evidence suggests that complex traits are likely determined by multiple loci, with each of which contributes a weak to moderate individual effect. Although extensive literature exists on multi-locus analysis of unrelated subjects, there are relatively fewer strategies for jointly analyzing multiple loci using family data. Here we address this issue by evaluating two pseudo-sibship methods: the 1:1 matching, which matches each affected offspring to the pseudo sibling formed by the alleles not transmitted to the affected offspring; the exhaustive matching, which matches each affected offspring to the pseudo siblings formed by all the other possible combinations of parental alleles. We prove that the two matching strategies use exactly and approximately the same amount of information from data under additive and multiplicative genetic models, respectively. Using numerical calculations under a variety of models and testing assumptions, we show that compared to the exhaustive matching, the 1:1 matching has comparable asymptotic power in detecting multiplicative / additive effects in single-locus analysis and main effects in multi-locus analysis, and it allows association testing of multiple linked loci. These results pave the way for many existing multi-locus analysis methods developed for the case-control (or matched case-control) design to be applied to case-parents data with minor modifications. As an example, with the 1:1 matching, we applied an L1 regularized regression to a Crohn’s disease dataset. Using the multiple loci selected by our approach, we obtained an order-of-magnitude decrease in p-value and an 18.9% increase in prediction accuracy when comparing to using the most significant individual locus.