Literature DB >> 28393390

A novel association test for multiple secondary phenotypes from a case-control GWAS.

Debashree Ray1, Saonli Basu2.   

Abstract

In the past decade, many genome-wide association studies (GWASs) have been conducted to explore association of single nucleotide polymorphisms (SNPs) with complex diseases using a case-control design. These GWASs not only collect information on the disease status (primary phenotype, D) and the SNPs (genotypes, X), but also collect extensive data on several risk factors and traits. Recent literature and grant proposals point toward a trend in reusing existing large case-control data for exploring genetic associations of some additional traits (secondary phenotypes, Y) collected during the study. These secondary phenotypes may be correlated, and a proper analysis warrants a multivariate approach. Commonly used multivariate methods are not equipped to properly account for the non-random sampling scheme. Current ad hoc practices include analyses without any adjustment, and analyses with D adjusted as a covariate. Our theoretical and empirical studies suggest that the type I error for testing genetic association of secondary traits can be substantial when X as well as Y are associated with D, even when there is no association between X and Y in the underlying (target) population. Whether using D as a covariate helps maintain type I error depends heavily on the disease mechanism and the underlying causal structure (which is often unknown). To avoid grossly incorrect inference, we have proposed proportional odds model adjusted for propensity score (POM-PS). It uses a proportional odds logistic regression of X on Y and adjusts estimated conditional probability of being diseased as a covariate. We demonstrate the validity and advantage of POM-PS, and compare to some existing methods in extensive simulation experiments mimicking plausible scenarios of dependency among Y, X, and D. Finally, we use POM-PS to jointly analyze four adiposity traits using a type 2 diabetes (T2D) case-control sample from the population-based Metabolic Syndrome in Men (METSIM) study. Only POM-PS analysis of the T2D case-control sample seems to provide valid association signals.
© 2017 WILEY PERIODICALS, INC.

Entities:  

Keywords:  GWAS; METSIM; case-control design; cross-phenotype association; joint modeling; multiple traits; multivariate analysis; propensity score; proportional odds model; secondary traits; stratification score

Mesh:

Substances:

Year:  2017        PMID: 28393390      PMCID: PMC5474176          DOI: 10.1002/gepi.22045

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  36 in total

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5.  Control for confounding in case-control studies using the stratification score, a retrospective balancing score.

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7.  A General and Robust Framework for Secondary Traits Analysis.

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8.  A simple and improved correction for population stratification in case-control studies.

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9.  An alternative hypothesis testing strategy for secondary phenotype data in case-control genetic association studies.

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10.  MultiPhen: joint model of multiple phenotypes can increase discovery in GWAS.

Authors:  Paul F O'Reilly; Clive J Hoggart; Yotsawat Pomyen; Federico C F Calboli; Paul Elliott; Marjo-Riitta Jarvelin; Lachlan J M Coin
Journal:  PLoS One       Date:  2012-05-02       Impact factor: 3.240

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2.  Methods for meta-analysis of multiple traits using GWAS summary statistics.

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3.  Effect of non-normality and low count variants on cross-phenotype association tests in GWAS.

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4.  Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes.

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Journal:  Genet Epidemiol       Date:  2019-09-23       Impact factor: 2.135

5.  An atlas of evidence-based phenotypic associations across the mouse phenome.

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Journal:  Sci Rep       Date:  2020-03-03       Impact factor: 4.379

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