Zaykin Dmitri V, Meng Zhaoling, Ehm Margaret G
National Institute of Environmental Health Sciences, National Institutes of Health.
Department of Biostatistics and Programming, Sanofi-Aventis, Bridgewater, NJ.
Am J Hum Genet. 2006 May;78(5):737-746. doi: 10.1086/503710. Epub 2006 Mar 13.
Identification and description of genetic variation underlying disease susceptibility, efficacy, and adverse reactions to drugs remains a difficult problem. One of the important steps in the analysis of variation in a candidate region is the characterization of linkage disequilibrium (LD). In a region of genetic association, the extent of LD varies between the case and the control groups. Separate plots of pairwise standardized measures of LD (e.g., D') for cases and controls are often presented for a candidate region, to graphically convey case-control differences in LD. However, the observed graphic differences lack statistical support. Therefore, we suggest the "LD contrast" test to compare whole matrices of disequilibrium between two samples. A common technique of assessing LD when the haplotype phase is unobserved is the expectation-maximization algorithm, with the likelihood incorporating the assumption of Hardy-Weinberg equilibrium (HWE). This approach presents a potential problem in that, in the region of genetic association, the HWE assumption may not hold when samples are selected on the basis of phenotypes. Here, we present a computationally feasible approach that does not assume HWE, along with graphic displays and a statistical comparison of pairwise matrices of LD between case and control samples. LD-contrast tests provide a useful addition to existing tools of finding and characterizing genetic associations. Although haplotype association tests are expected to provide superior power when susceptibilities are primarily determined by haplotypes, the LD-contrast tests demonstrate substantially higher power under certain haplotype-driven disease models.
识别和描述疾病易感性、药物疗效及不良反应背后的基因变异仍是一个难题。分析候选区域变异的重要步骤之一是连锁不平衡(LD)的特征描述。在基因关联区域,病例组和对照组之间的LD程度有所不同。通常会针对候选区域分别绘制病例组和对照组的成对标准化LD测量值(如D')图,以直观呈现病例组与对照组在LD方面的差异。然而,观察到的图形差异缺乏统计学支持。因此,我们建议采用“LD对比”检验来比较两个样本间的不平衡整体矩阵。当单倍型相位未知时,评估LD的常用技术是期望最大化算法,其似然性纳入了哈迪-温伯格平衡(HWE)假设。这种方法存在一个潜在问题,即在基因关联区域,基于表型选择样本时,HWE假设可能不成立。在此,我们提出一种不假定HWE的计算可行方法,同时给出图形展示以及病例组与对照组样本间成对LD矩阵的统计比较。LD对比检验为现有寻找和描述基因关联的工具增添了有用内容。尽管当易感性主要由单倍型决定时,单倍型关联检验预期具有更高的效能,但在某些单倍型驱动的疾病模型下,LD对比检验显示出显著更高的效能。