Zhou Hui, Pan Wei
Division of Biostatistics, University of Minnesota, Minneapolis, MN 55455, USA.
Ann Hum Genet. 2009 Nov;73(Pt 6):614-30. doi: 10.1111/j.1469-1809.2009.00542.x. Epub 2009 Sep 1.
Most of the existing association tests for population-based case-control studies are based on comparing the mean genotype scores between the case and control groups, which may not be efficient under genetic heterogeneity. Given that most common diseases are genetically heterogeneous, caused by mutations in multiple loci, it may be beneficial to fully account for genetic heterogeneity in an association test. Here we first propose a binomial mixture model for such a purpose and develop a corresponding mixture likelihood ratio test (MLRT) for a single locus. We also consider two methods to combine single-locus-based MLRTs across multiple loci in linkage disequilibrium to boost power when causal SNPs are not genotyped. We show with a wide spectrum of numerical examples that under genetic heterogeneity the proposed tests are more powerful than some commonly used association tests.
大多数现有的基于人群的病例对照研究的关联检验是基于比较病例组和对照组之间的平均基因型得分,在遗传异质性情况下这可能效率不高。鉴于大多数常见疾病是遗传异质性的,由多个位点的突变引起,在关联检验中充分考虑遗传异质性可能是有益的。在此,我们首先为此目的提出一个二项混合模型,并针对单个位点开发相应的混合似然比检验(MLRT)。我们还考虑了两种方法,用于在连锁不平衡的多个位点上组合基于单个位点的MLRT,以便在未对因果单核苷酸多态性(SNP)进行基因分型时提高检验效能。我们通过广泛的数值示例表明,在遗传异质性情况下,所提出的检验比一些常用的关联检验更具效能。