Morris Richard W, Kaplan Norman L
Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709-2233, USA.
Genet Epidemiol. 2002 Oct;23(3):221-33. doi: 10.1002/gepi.10200.
We investigated the effect of multiple susceptibility alleles at a single disease locus on the statistical power of a likelihood ratio test to detect association between alleles at a marker locus and a disease phenotype in a case-control design. Using simplifying assumptions to obtain the joint frequency distribution of marker and disease locus alleles, we present numerical results that illustrate the impact of historical variation of initial associations between marker alleles and susceptibility alleles on the power of a likelihood ratio test for association. Our results show that an increase in the number of susceptibility alleles produces a decrease in power of the likelihood ratio test. The decrease in power in the presence of multiple susceptibility alleles, however, is less for markers with multiple alleles than for markers with two alleles. We investigate the implications of this observation for tests of association based on haplotypes made up of tightly linked single-nucleotide polymorphisms (SNPs). Our results suggest that an analysis based on haplotypes can be advantageous over an analysis based on individual SNPs in the presence of multiple susceptibility alleles, particularly when linkage disequilibria between SNPs is weak. The results provide motivation for further development of statistical methods based on haplotypes for assessing the potential for association methods to identify and locate complex disease genes.
我们研究了单一疾病位点上多个易感等位基因对似然比检验统计功效的影响,该检验用于在病例对照设计中检测标记位点等位基因与疾病表型之间的关联。通过使用简化假设来获得标记和疾病位点等位基因的联合频率分布,我们给出了数值结果,这些结果说明了标记等位基因与易感等位基因之间初始关联的历史变化对关联似然比检验功效的影响。我们的结果表明,易感等位基因数量的增加会导致似然比检验的功效降低。然而,对于具有多个等位基因的标记,在存在多个易感等位基因时功效的降低幅度小于具有两个等位基因的标记。我们研究了这一观察结果对基于紧密连锁单核苷酸多态性(SNP)组成的单倍型进行关联检验的意义。我们的结果表明,在存在多个易感等位基因的情况下,基于单倍型的分析可能比基于单个SNP的分析更具优势,特别是当SNP之间的连锁不平衡较弱时。这些结果为进一步开发基于单倍型的统计方法提供了动力,以评估关联方法识别和定位复杂疾病基因的潜力。