Abstract

BackgroundComplex traits may be defined by a range of different criteria. It would result in a loss of information to perform analyses simply on the basis of a final clinical dichotomized affected / unaffected variable.ResultsWe assess the performance of four alternative approaches for the analysis of multiple phenotypes in genetic association studies. We describe the four methods in detail and discuss their relative theoretical merits and disadvantages. Using simulation we demonstrate that PCA provides the greatest power when applied to both correlated phenotypes and with large numbers of phenotypes. The multivariate approach had low type I error only with independent phenotypes or small numbers of phenotypes. In this study, our application of the four methods to schizophrenia data provides converging evidence of the relative performance of the methods.ConclusionsVia power analysis of simulated data and testing of experimental data, we conclude that PCA, creating one variable based on a linear combination of all the traits, performs optimally. We propose that our comparison will provide insight into the properties of the methods and help researchers to choose appropriate strategy in future experimental studies.

Highlights

  • Complex traits may be defined by a range of different criteria

  • Through power analysis of extensively simulated data and a real data application, we conclude that for genetic association studies, using principal component analysis (PCA) to create one variable based on a linear combination of all the traits performs optimally

  • PCA results in the smallest p-value of 0.002

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Summary

Introduction

Complex traits may be defined by a range of different criteria It would result in a loss of information to perform analyses on the basis of a final clinical dichotomized affected / unaffected variable. For linkage and genetic association studies of biological markers, a complex trait can be defined by a range of multiple and often overlapping criteria. A meta-analysis of 61 studies concluded that multiple loci affect WHR independently of BMI [2]. In this example, WHR and BMI may reflect different aspects of the Multiple intermediate phenotypes have been proposed for a variety of neuropsychiatric disorders, in particular schizophrenia, bipolar disorder, and Alzheimer’s disease. When subjects clinically are diagnosed as either affected or unaffected for a disorder, this dichotomization may lead to a loss of power in genetic analyses

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