Abstract

BackgroundThe genetic association analysis using haplotypes as basic genetic units is anticipated to be a powerful strategy towards the discovery of genes predisposing human complex diseases. In particular, the increasing availability of high-resolution genetic markers such as the single-nucleotide polymorphisms (SNPs) has made haplotype-based association analysis an attractive alternative to single marker analysis.ResultsWe consider haplotype association analysis under the population-based case-control study design. A multinomial logistic model is proposed for haplotype analysis with unphased genotype data, which can be decomposed into a prospective logistic model for disease risk as well as a model for the haplotype-pair distribution in the control population. Environmental factors can be readily incorporated and hence the haplotype-environment interaction can be assessed in the proposed model. The maximum likelihood estimation with unphased genotype data can be conveniently implemented in the proposed model by applying the EM algorithm to a prospective multinomial logistic regression model and ignoring the case-control design. We apply the proposed method to the hypertriglyceridemia study and identifies 3 haplotypes in the apolipoprotein A5 gene that are associated with increased risk for hypertriglyceridemia. A haplotype-age interaction effect is also identified. Simulation studies show that the proposed estimator has satisfactory finite-sample performances.ConclusionOur results suggest that the proposed method can serve as a useful alternative to existing methods and a reliable tool for the case-control haplotype-based association analysis.

Highlights

  • The genetic association analysis using haplotypes as basic genetic units is anticipated to be a powerful strategy towards the discovery of genes predisposing human complex diseases

  • We show that the proposed multinomial logistic model can be decomposed into a prospective logistic disease model relating the haplotype and environmental factors with disease, as well as a parametric model for the haplotype-pair distribution, conditional on the environmental covariates, among the control population

  • One primary objective of this study is to assess the association between the haplotypes in apolipoprotein A5 gene (APOA5) and hypertriglyceridemia in humans, adjusting for the environmental covariates Age, Sex, and BMI, and to explore the potential haplotype-environment interactions

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Summary

Introduction

The genetic association analysis using haplotypes as basic genetic units is anticipated to be a powerful strategy towards the discovery of genes predisposing human complex diseases. The increasing availability of high-resolution genetic markers such as the single-nucleotide polymorphisms (SNPs) has made haplotype-based association analysis an attractive alternative to single marker analysis. It is anticipated that greater power may be gained by utilizing linkage-disequilibrium information from multiple markers simultaneously. This anticipation, together with recent advances of the availability of high-resolution genetic markers, in particular the single-nucleotide polymorphisms (SNPs), has motivated the use of haplotypes, which are specific combinations of closely linked genetic markers on a chromosome, as the basic genetic units for association analysis. Schaid [1] provided a detailed and excellent review for haplotype-based association analysis

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