Abstract
Though multiple interacting loci are likely involved in the etiology of complex diseases, early genome-wide association studies (GWAS) have depended on the detection of the marginal effects of each locus. Here, we evaluate the power of GWAS in the presence of two linked and potentially associated causal loci for several models of interaction between them and find that interacting loci may give rise to marginal relative risks that are not generally considered in a one-locus model. To derive power under realistic situations, we use empirical data generated by the HapMap ENCODE project for both allele frequencies and linkage disequilibrium (LD) structure. The power is also evaluated in situations where the causal single nucleotide polymorphisms (SNPs) may not be genotyped, but rather detected by proxy using a SNP in LD. A common simplification for such power computations assumes that the sample size necessary to detect the effect at the tSNP is the sample size necessary to detect the causal locus directly divided by the LD measure r(2) between the two. This assumption, which we call the "proportionality assumption", is a simplification of the many factors that contribute to the strength of association at a marker, and has recently been criticized as unreasonable (Terwilliger and Hiekkalinna [2006] Eur J Hum Genet 14(4):426-437), in particular in the presence of interacting and associated loci. We find that this assumption does not introduce much error in single locus models of disease, but may do so in so in certain two-locus models.
MeSH Terms
Genetic Predisposition to Disease
Genome, Human/genetics
Genotype
Humans
Linkage Disequilibrium
Models, Genetic
Polymorphism, Single Nucleotide
Quantitative Trait Loci/genetics
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pickrell Joseph
INSERM, U535, Villejuif, France.
Clerget-Darpoux Françoise
Bourgain Catherine
References (29)
29 references, click to expand
-
Complement factor H polymorphism in age-related macular degeneration.
Science. 2005 Apr 15;308(5720):385-9
PMID: 15761122
-
Genome-wide strategies for detecting multiple loci that influence complex diseases.
Nat Genet. 2005 Apr;37(4):413-7
PMID: 15793588
-
Comparison of population- and family-based methods for genetic association analysis in the presence of interacting loci.
Genet Epidemiol. 2005 Jul;29(1):51-67
PMID: 15892093
-
Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix.
Heredity (Edinb). 2005 Sep;95(3):221-7
PMID: 16077740
-
A haplotype map of the human genome.
Nature. 2005 Oct 27;437(7063):1299-320
PMID: 16255080
-
Population structure, differential bias and genomic control in a large-scale, case-control association study.
Nat Genet. 2005 Nov;37(11):1243-6
PMID: 16228001
-
Efficiency and power in genetic association studies.
Nat Genet. 2005 Nov;37(11):1217-23
PMID: 16244653
-
Common deletions and SNPs are in linkage disequilibrium in the human genome.
Nat Genet. 2006 Jan;38(1):82-5
PMID: 16327809
-
An utter refutation of the "fundamental theorem of the HapMap".
Eur J Hum Genet. 2006 Apr;14(4):426-37
PMID: 16479260
-
Evaluating and improving power in whole-genome association studies using fixed marker sets.
Nat Genet. 2006 Jun;38(6):663-7
PMID: 16715096
-
Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
Am J Hum Genet. 2006 Aug;79(2):275-90
PMID: 16826518
-
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
Nat Genet. 2006 Sep;38(9):1049-54
PMID: 16936733
-
Two-stage two-locus models in genome-wide association.
PLoS Genet. 2006 Sep 22;2(9):e157
PMID: 17002500
-
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
Science. 2006 Dec 1;314(5804):1461-3
PMID: 17068223
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
Nature. 2001 May 31;411(6837):599-603
PMID: 11385576
-
Are rare variants responsible for susceptibility to complex diseases?
Am J Hum Genet. 2001 Jul;69(1):124-37
PMID: 11404818
-
Linkage disequilibrium in humans: models and data.
Am J Hum Genet. 2001 Jul;69(1):1-14
PMID: 11410837
-
On the allelic spectrum of human disease.
Trends Genet. 2001 Sep;17(9):502-10
PMID: 11525833
-
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease.
Am J Hum Genet. 2002 Apr;70(4):845-57
PMID: 11875755
-
The allelic architecture of human disease genes: common disease-common variant...or not?
Hum Mol Genet. 2002 Oct 1;11(20):2417-23
PMID: 12351577
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease.
Nat Genet. 2003 Feb;33(2):177-82
PMID: 12524541
-
Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power.
Hum Hered. 2003;56(1-3):18-31
PMID: 14614235
-
The ubiquitous nature of epistasis in determining susceptibility to common human diseases.
Hum Hered. 2003;56(1-3):73-82
PMID: 14614241
-
The complex interplay among factors that influence allelic association.
Nat Rev Genet. 2004 Feb;5(2):89-100
PMID: 14735120
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol.
Science. 2004 Aug 6;305(5685):869-72
PMID: 15297675
-
Prospects for whole-genome linkage disequilibrium mapping of common disease genes.
Nat Genet. 1999 Jun;22(2):139-44
PMID: 10369254
-
Haploview: analysis and visualization of LD and haplotype maps.
Bioinformatics. 2005 Jan 15;21(2):263-5
PMID: 15297300
-
Genome-wide association studies: theoretical and practical concerns.
Nat Rev Genet. 2005 Feb;6(2):109-18
PMID: 15716907
-
Lack of MEF2A mutations in coronary artery disease.
J Clin Invest. 2005 Apr;115(4):1016-20
PMID: 15841183