Genetic Epidemiology · 2004 · 229 citations · 42 references
Life SciencesBiostatisticsGeneticsGenetic EpidemiologyHuman GeneticsStatistical GeneticsDisease Susceptibility LociGene InteractionGene-environment InteractionGenotype-phenotype Association AnalysisHaplotype AnalysisAssociation Between Linked Markers And TraitsConditional Association AnalysisConditional Genetic Interaction AnalysisEpistatic InteractionsHaplotype-based Association AnalysisParental Genetic EffectsPopulation Stratification AdjustmentPopulation Stratification Correction
Genetic association studies often use case‑parent trios and pseudocontrols derived from untransmitted alleles, applying conditional logistic regression to avoid estimating nuisance parameters and to mitigate population stratification. The authors extend this framework to test epistatic interactions at unlinked loci, parent‑of‑origin effects, and gene‑environment interactions. They relax conditioning on parental genotypes to allow parental genotype exchangeability, thereby increasing power for detecting parent‑of‑origin effects. Simulations indicate limited power to distinguish parent‑of‑origin effects from mother‑child genotype interaction effects.
Abstract Estimation and testing of genetic effects (genotype relative risks) are often performed conditionally on parental genotypes, using data from case‐parent trios. This strategy avoids having to estimate nuisance parameters such as parental mating type frequencies, and also avoids generating spurious results due to confounding causes of association such as population stratification. For effects at a single locus, the resulting analysis is equivalent to matched case/control analysis via conditional logistic regression, using the case and three “pseudocontrols” derived from the untransmitted parental alleles. We previously showed that a similar approach can be used for analyzing genotype and haplotype effects at a set of closely linked loci, but with a required adjustment to the conditioning argument that results in varying numbers of pseudocontrols, depending on the disease model that is to be fitted. Here we extend this method to include the analysis of epistatic effects (gene‐gene interactions) at unlinked loci, to include parent‐of‐origin effects at one or more loci, and to allow additional incorporation of gene‐environment interactions. The conditional logistic approach provides a natural and flexible framework for incorporating these additional effects. By relaxing the conditioning on parental genotypes to allow exchangeability of parental genotypes, we show how the power of this approach can be increased when studying parent‐of‐origin effects. Simulations suggest that there is limited power to distinguish between parent‐of‐origin effects and effects due to interaction between genotypes of mother and child. © 2004 Wiley‐Liss, Inc.
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Maximum Likelihood Estimation of Misspecified Models
Halbert White · Econometrica · 1982 · 4.1K citations
Maximum Likelihood Estimation of Misspecified Models
Halbert White · Econometrica · 1983 · 3.8K citations