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A general approach to testing for pleiotropy with rare and common variants.

ABSTRACT: Through genome-wide association studies, numerous genes have been shown to be associated with multiple phenotypes. To determine the overlap of genetic susceptibility of correlated phenotypes, one can apply multivariate regression or dimension reduction techniques, such as principal components analysis, and test for the association with the principal components of the phenotypes rather than the individual phenotypes. However, as these approaches test whether there is a genetic effect for at least one of the phenotypes, a significant test result does not necessarily imply pleiotropy. Recently, a method called Pleiotropy Estimation and Test Bootstrap (PET-B) has been proposed to specifically test for pleiotropy (i.e., that two normally distributed phenotypes are both associated with the single nucleotide polymorphism of interest). Although the method examines the genetic overlap between the two quantitative phenotypes, the extension to binary phenotypes, three or more phenotypes, and rare variants is not straightforward. We provide two approaches to formally test this pleiotropic relationship in multiple scenarios. These approaches depend on permuting the phenotypes of interest and comparing the set of observed P-values to the set of permuted P-values in relation to the origin (e.g., a vector of zeros) either using the Hausdorff metric or a cutoff-based approach. These approaches are appropriate for categorical and quantitative phenotypes, more than two phenotypes, common variants and rare variants. We evaluate these approaches under various simulation scenarios and apply them to the COPDGene study, a case-control study of chronic obstructive pulmonary disease in current and former smokers.

SUBMITTER: Lutz SM

PROVIDER: S-EPMC5472207 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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A general approach to testing for pleiotropy with rare and common variants.

Lutz Sharon M SM Fingerlin Tasha E TE Hokanson John E JE Lange Christoph C

Genetic epidemiology 20161130 2

Through genome-wide association studies, numerous genes have been shown to be associated with multiple phenotypes. To determine the overlap of genetic susceptibility of correlated phenotypes, one can apply multivariate regression or dimension reduction techniques, such as principal components analysis, and test for the association with the principal components of the phenotypes rather than the individual phenotypes. However, as these approaches test whether there is a genetic effect for at least ...[more]

PMID: 27900789

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Project description:BackgroundLanguage plays a major role in human behavior. For this reason, neurodevelopmental and psychiatric disorders in which linguistic ability is impaired could have a big impact on the individual's social interaction and general wellbeing. Such disorders tend to have a strong genetic component, but most past studies examined mostly the linguistic overlaps across these disorders; investigations into their genetic overlaps are limited. The aim of this study was to assess the potential genetic overlap between language impairment and broader behavioral disorders employing methods capturing both common and rare genetic variants.MethodsWe employ polygenic risk scores (PRS) trained on specific language impairment (SLI) to evaluate genetic overlap across several disorders in a large case-cohort sample comprising ~13,000 autism spectrum disorder (ASD) cases, including cases of childhood autism and Asperger's syndrome, ~15,000 attention deficit/hyperactivity disorder (ADHD) cases, ~3000 schizophrenia cases, and ~21,000 population controls. We also examine rare variants in SLI/language-related genes in a subset of the sample that was exome-sequenced using the SKAT-O method.ResultsWe find that there is little evidence for genetic overlap between SLI and ADHD, schizophrenia, and ASD, the latter being in line with results of linguistic analyses in past studies. However, we observe a small, significant genetic overlap between SLI and childhood autism specifically, which we do not observe for SLI and Asperger's syndrome. Moreover, we observe that childhood autism cases have significantly higher SLI-trained PRS compared to Asperger's syndrome cases; these results correspond well to the linguistic profiles of both disorders. Our rare variant analyses provide suggestive evidence of association for specific genes with ASD, childhood autism, and schizophrenia.ConclusionsOur study provides, for the first time, to our knowledge, genetic evidence for ASD subtypes based on risk variants for language impairment.

Dataset Information

A general approach to testing for pleiotropy with rare and common variants.

Publications

A general approach to testing for pleiotropy with rare and common variants.

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